中国西南六种广义拂子茅属(禾本科)植物的染色体数目

广义拂子茅属（Calamagrostis）是一个世界温带广布的大属,有些作者又分为拂子茅属和野青茅属,但近期的研究表明处理为一个属较为合适。中国共有37种广义拂子茅属植物,但至今没有任何染色体的研究。本文报道了其中产于中国西南6种野青茅的染色体数目,其中Deyeuxia petelotii 4个居群,D．diffusa,D．moupinemis,D．nivicola和D．flvens各一个居群都是四倍体（2n=4x=28）,D．neglecta为六倍体（2n=6x=42）。根据广义拂子茅属植物染色体倍性特征,该属植物中至今未发现二倍体,四倍体是该属中倍性最低和最普遍的,广义拂子茅属的演化很可能是在四倍体的水平上进行的。由于以上几个四倍体种均是狭域分布的类群,所以可能是由四倍体的祖先隔离分化形成的。     

国产驴蹄草的细胞地理学研究（英文）

为探讨国产毛茛科(Ranunculaceae)驴蹄草属(Caltha)两种植物的演化,该文利用传统染色体压片技术和流式细胞术,并结合前人染色体研究结果,对我国驴蹄草23个居群和花葶驴蹄草10个居群进行了细胞学研究。结果表明:驴蹄草是由四倍体(2n=4x=32)、六倍体(2n=6x=48)和八倍体(2n=8x=64)构成的多倍体复合群,花葶驴蹄草具有四倍体(2n=4x=32)和八倍体(2n=8x=64)两种倍性水平。驴蹄草和花葶驴蹄草均是四倍体较为常见,目前尚未见有二倍体报道。由于驴蹄草和花葶驴蹄草大部分居群采自中国青藏高原地区,可能在冰期时存在古二倍体,其适应性较弱,逐渐被其他的倍性取代,这是由于不同细胞型对环境适应性的结果。驴蹄草可能存在两条进化路线:一条是从甘肃到达云南;另一条是从西藏到达云南。前期分子系统学研究显示花葶驴蹄草与驴蹄草的亲缘关系较近,该研究结果中花葶驴蹄草染色体比驴蹄草要小,花葶驴蹄草可能比驴蹄草相对进化。目前花葶驴蹄草只有10个居群,还需进一步增加居群量来解析其演化路线。     

国产驴蹄草的细胞地理学研究

为探讨国产毛茛科(Ranunculaceae)驴蹄草属(Caltha)两种植物的演化,该文利用传统染色体压片技术和流式细胞术,并结合前人染色体研究结果,对我国驴蹄草23个居群和花葶驴蹄草10个居群进行了细胞学研究。结果表明:驴蹄草是由四倍体(2n=4x=32)、六倍体(2n=6x=48)和八倍体(2n=8x=64)构成的多倍体复合群,花葶驴蹄草具有四倍体(2n=4x=32)和八倍体(2n=8x=64)两种倍性水平。驴蹄草和花葶驴蹄草均是四倍体较为常见,目前尚未见有二倍体报道。由于驴蹄草和花葶驴蹄草大部分居群采自中国青藏高原地区,可能在冰期时存在古二倍体,其适应性较弱,逐渐被其他的倍性取代,这是由于不同细胞型对环境适应性的结果。驴蹄草可能存在两条进化路线:一条是从甘肃到达云南;另一条是从西藏到达云南。前期分子系统学研究显示花葶驴蹄草与驴蹄草的亲缘关系较近,该研究结果中花葶驴蹄草染色体比驴蹄草要小,花葶驴蹄草可能比驴蹄草相对进化。目前花葶驴蹄草只有10个居群,还需进一步增加居群量来解析其演化路线。     

3种香薷属植物染色体数目与核型分析

参照植物根尖细胞学研究的方法标准,对香薷属3种(5个居群)植物进行核形态学分析。结果表明:(1)从染色体数目看,密花香薷2居群染色体数目2n=16;野苏子2居群染色体数目2n=20,染色体数目和倍性与前人报道的一致;毛穗香薷染色体数目2n=10为首次报道。(2)聚类分析结果显示,3种(5居群)植物中野苏子和密花香薷亲缘关系较近;结合现有报道数据分析表明,该属植物仅有2种倍性(二倍体和四倍体),且二倍体占主导地位。(3)核型参数分析表明:密花香薷的稻城无名山居群1核型公式为2n=2x=16=14m+2sm,居群2为2n=2x=16=16m,着丝粒指数(CI)分别为39.57和42.32,不对称系数AI值分别为2.75和2.87,核型不对称性都为1A型;毛穗香薷的核型公式为2n=2x=10=10m,着丝粒指数(CI)为41.76,不对称系数AI值为5.25,核型不对称性为1B型;野苏子的昆明西山居群核型公式为2n=2x=20=14m+6sm,聂拉木樟木沟居群为2n=2x=20=16m+4sm,着丝粒指数(CI)分别为38.49和40.97,不对称系数AI值为4.20和4.30,核型不对称性为1B型和2B型。     

六倍体多星韭的发现及多星韭种内倍性组成及演化的分析

采用染色体常规制片技术,对云南西北部和中部地区11个多星韭居群进行了细胞学分析。结果显示:(1)云南西北部多星韭二倍体、四倍体混合分布的太子阁和华首门四倍体居群中发现了三倍体(2n=3x=21),核型公式分别为:2n=3x=21=[6m(2sat)+8sm]+(3m+4sm)和2n=3x=21=[4m(2sat)+10sm]+(2m+4sm+lst)。三倍体含2条随体染色体,它的21条染色体含2个同源染色体组和一个与它们同源性稍差的染色体组。(2)在云南中部的多星韭四倍体居群中首次发现了六倍体,核型公式为2n=6x=42=15m(3sat)+27sm,核型类型2A。(3)结合核型特征及地理分布对多星韭三倍体和六倍体的成因进行分析,提示多星韭三倍体来源于二倍体与四倍体的杂交,六倍体是通过四倍体产生的未减数配子(n=4x=28)与正常减数配子(n=2x=14)的结合形成的。本研究结果支持多星韭的分化中心是云南西北部高海拔地区的观点,并结合前人的研究和本工作的结果,对多星韭种内的倍性组成和演化进行了分析和讨论。     

中国西南部菖蒲属的细胞学研究，兼论菖蒲的细胞地理

通过对中国西南部3种菖蒲属（Acorus L.）植物（菖蒲A.calamus L.、石菖蒲A.tatarinowii Schott和金钱蒲A.gramineus Soland.）的细胞学研究,发现分布在运动及四川的9个菖蒲居群中,有5个居群为四倍体（2n=4x=44）,4个居群为六倍体（2n=6x=66）。其中四倍体见于滇南及川西南;六倍体见于滇中及滇西北,并为首次报道。在云南及贵州分布的石菖蒲及金钱蒲5个居群均为二倍体。讨论了菖蒲分布区从二倍本、三倍体、四倍体和六倍体4种不同倍性居群的分布规律和可能的演化关系,六倍体居群的产生很可能喜马拉雅造山运动有关。     

八种国产葱属植物染色体研究

本文对国产葱属Allium 8个种的14个居群的染色体进行了研究。其染色体基数均为x=8,其中7个居群为二倍体(2n=2x=16),6个居群为四倍体(2n=4x=32),1个居群为多倍体复合体(2n=4x=32,2n=6x=48,2n=8x=64和2n=9x=72)。并发现随体染色体十分活跃,在多倍体中其数目并不都与其倍性相对应,并有“串状随体”现象出现;在有些类群中其形态变异较大,而随体染色体杂合形式的多态现象也较普遍。本文重点讨论了随体染色体的数目、形态变异及杂合现象在葱属进化中的作用,认为随体染色体形态变异及杂合现象的出现是葱属中遗传变异的重要源泉之一。并对葱属中的染色体基数及种内多倍性问题进行了初步讨论。     

昆明地区滇韭形态及染色体多态性研究

对昆明地区滇韭的 8个当地居群开展了形态及核型研究 ,并对形态及染色体性状进行了巢式方差分析。结果表明 :滇韭的形态性状在居群内具丰富多态性 ,在居群间具明显多型性 ;核型较对称 ,存在两种倍性的分化 :梁王山居群为二倍体 (2x) ,昆明居群为四倍体(4x)。二倍体核型公式为K (2n ) =2x =16 =14m 2sm ,四倍体核型公式为K (2n ) =4x =32=2 8m 4sm。滇韭的染色体因存在倍性变化、B -染色体形态和数目变化及随体染色体的形态和大小变化而具有一定程度的多态性。     

禾本科广义拂子茅属的叶表皮形态研究

禾本科广义拂子茅属Calamagrostis Adans. s.l.是广布于全球温带和热带亚热带高山的一个大属, 常分为拂子茅属Calamagrostis Adans. s.s.和野青茅属Deyeuxia Beauv.。对国产5种拂子茅属和26种、1变种野青茅属植物在光镜下进行了叶表皮特征的观察。发现广义拂子茅属植物的叶表皮特征为典型的狐茅型, 很多结构在种间有丰富的变异式样, 如脉间长细胞形状、大小和细胞壁的厚度与弯曲程度, 短细胞形状和分布式样, 硅质体形状和分布式样, 气孔形状和分布式样, 以及刺毛形态和分布式样等。在国产种类中首次发现微乳突结构, 在很多种类中发现刺毛硅质化现象。用UPGMA对15个叶表皮性状进行分析, 结果分为两大支: 具加厚的长细胞、密集分布的短细胞和(或)刺毛以及刺毛硅质化的种类聚为一支; 具薄壁的长细胞、较稀疏的短细胞和(或)刺毛以及刺毛不发生硅质化的种类聚为另一支。这种分异与广义拂子茅属的属下系统相关性不大, 但与种的海拔分布有关。前一支的种类大多生长于高海拔(2600 m以上)地区, 而后一支的种类则大多生长在低海拔(2600 m以下)地区。     

中国西南地区6种植物的核型研究及其系统学意义

采用植物细胞学研究方法对主要采自中国西南地区横断山的6种植物:扁核木(Prinsepia utilis)、小叶金露梅(Potentilla parvifolia)、峨眉繁缕(Stellaria omeiensis)、金铁锁(Psammosilene tunicoides)、山卷耳(Cerastium pusillum)和独尾草(Eremurus chinensis)进行染色体数目和核型研究。研究表明:(1)6个种的核型公式和不对称性如下:扁核木2n=2x=30=1M+20m+9sm,2A;小叶金露梅2n=2x=28=21m+7sm,2B;峨眉繁缕2n=8x=72=1M+71m,1B;金铁锁在同居群下有倍性变化,2n=2x=14=14m,1A和2n=4x=28=28m,1A;山卷耳2n=2x=24=24m(2sat),1A;独尾草2n=2x=14=2m+2sm+8st+2t,4B。(2)讨论了染色体资料在这些物种分类和系统上的意义,支持扁核木为李亚科下的扁核木属;位于委陵菜属木本系的小叶金露梅主要以二倍体和四倍体为主,而草本系的委陵菜属植物多为多倍体。(3)该研究首次报道峨眉繁缕为八倍体,是繁缕属发现的最高倍性的物种;对比金铁锁属与蝇子草属的染色体研究发现,金铁锁属可能是由它们的共同祖先通过非整倍化产生;该研究首次发现山卷耳存在染色体数目2n=24的情况,且有1对随体;独尾草的研究进一步证明该物种可能为二型核。     

中国野青茅属(禾本科)一些种类的修订

在标本室研究和野外考察的基础上,对中国野青茅属的一些种类进行了修订。首次归并了5个类群,即将Deyeuxia pulchella var． laxa P．C．Kuo et S．L. Lu,D．gyirongensis P．C. Kuo et S．L．Lu,Calamagrostis megalantha Keng ex Keng f.并入 D. pulchella (Griseb.)Hook．f.作为异名;将D．venusta Keng,Calamagrostis longiflora Keng ex Keng f．并入D.flavens Keng作为异名;并确认D. compacta Munro ex Hook．f.与D.holciformis (Jaub．et Spach．)Bor是同一种。     

Correlation between distyly and ploidy level in Damnacanthus (Rubiaceae)

Somatic chromosomes were observed in 661 individuals of 14 taxa, nine species and five varieties, of Damnacanthus (Rubiaceae). Chromosome numbers are reported for the first time for 13 taxa. Diploid (2n = 22) and tetraploid (2n = 44) counts were obtained. Distyly is reported for the first time for four species, D. angustifolius, D. henryi, D. labordei, and D. officinarum. A strong correlation exists between chromosome number and occurrence of distyly. Regardless of taxa in Damnacanthus, distylous populations are diploid, and monomorphic populations are tetraploid. Flowers of the monomorphic populations observed have a long style and short stamens with few exceptions. Polyploidization may have caused the breakdown of distylous to monomorphic flowers. In D. indicus, leaves from the tetraploid populations tend to be larger than those from the diploid populations. Populations of tetraploid D. indicus were distributed in more northern areas than those of the diploid. Three types of sympatric distribution were found for the varieties of D. indicus in Japan: diploid and tetraploid, two diploids, and two tetraploids. Based on the present chromosome number study, the taxonomy of the varieties of D. indicus should be revised.     

Cytogeography of the South American Turnera sidoides L. complex (Turneraceae, Leiocarpae)

New chromosome number determinations are presented for 48 populations of five subspecies of Turnera sidoides. Chromosome counts in sspp. carnea, holosericea, integrifolia and sidoides confirm previous data while, in ssp. pinnatifida , the numbers 2n=2x = 14 and 2n = 6x = 42 are reported for the first time. The results show that polyploidy is a very frequent phenomenon. Populations are primarily tetraploids (2n = 4x = 28), while diploids (2n = 2x = 14), hexaploids (2n = 6x =42) and octoploids (2rc = 8x = 56) are less frequent. Diploid, tetraploid and hexaploid cytotypes occur in sspp. carnea and pinnatifida , whereas tetraploids and hexaploids are known in ssp. holosericea. Turnera sidoides ssp. integrifolia shows a polyploid series with ploidy levels from 2x to 8x. The ssp. sidoides appears to be uniformly tetraploid, with the exception of an isolated pentaploid (2rc = 5x = 35). On the basis of these counts and previous reports the geographical distribution of the cytotypes has been determined and related to climatic and ecological factors.     

A cytotaxonomic study of theCalamagrostis purpurea —langsdorffii—canadensis complex in the lowlands of hokkaido

A chromosome survey of 278 individuals from 52 localities confirmed, that the principal components of theCalamagrostis purpurea—langsdorffi—canadensis complex in the lowlands of Hokkaido are tetraploid (2n=28) and octoploid (2n=56). A few hexploids (2n=42), were also found, but they may be either a triploid of the tetraploid plants or a hybrid between the tetraploid and octoploid plants. These hexaploids clearly differ in origin from the North American plants with 2n=42 which are generally placed underC. canadensis. The tetraploids and the octoploids are significantly different in pollen size but resemble each other in other morphological features and ecological requirements. These two races are also not disparate in distribution within Hokkaido. The tetraploids in Hokkaido are closely related to the tetraploids known in Alaska, and these tetraploid plants may be continuously distributed from Hokkaido to Alaska. The octoploids in Hokkaido have shown good pollen. They seem to have had a somewhat different course of evolution fromC. purpurea s. str. which principally reproduces in an apomictic manner.     

二倍体铁破锣的核型及四倍体细胞型的首次发现

本文重新检查了铁破锣的核型。来自湖南新宁的40个个体中,1个个体为四倍体,其核型公式为2n＝4x=32=16m+8sm+4st+4t;其余个体为二倍体,其核型公式为2n＝2x＝16=8m+4sm+2st+2t。来自云南大理的10个个体全为四倍体,其核型公式为2n=4x=32＝16m+8sm+4st+4t。据此认为商效民(1985)报道的该种的核型分析结果有误。他至少将第4对染色体的着丝点位置辨认错了。该对染色体不具有中部着丝点而实际上具有近端部着丝点。本文还比较了铁破锣和角叶铁破锣的核型差异,并详细讨论了铁破锣属的系统位置。     

Natural and induced polyploidy in Acacia dealbata Link. and Acacia mangium Willd

Seeds were obtained from seven natural populations of Acacia dealbata, three natural populations of A. mangium and a seed orchard of A. mangium, representing the natural range of the two species. Polyploids were discovered in two of the seven populations of A. dealbata. The 2C DNA amount for diploid A. dealbata (2n = 2x = 26) was 1.74 pg, and for diploid A. mangium (2n = 2x = 26) was 1.30 pg. A naturally occurring tetraploid of A. dealbata (2n = 4x = 52) had a 2C DNA amount of 3.41 pg and a naturally occurring triploid genotype had a 2C DNA amount of 2.53 pg. The use of colchicine and oryzalin was investigated as a means of producing higher frequencies of tetraploids of both A. mangium and A. dealbata for incorporation into breeding programmes. Colchicine treatment gave tetraploid frequencies up to 29% for A. dealbata seedlings, and up to 18% for A. mangium seedlings. In contrast, no tetraploid A. mangium was detected following oryzalin treatment, and the low frequencies of tetraploids observed in A. dealbata could be attributed to their natural occurrence.     

A Cytogeographical Study on Clintonia udensis (Liliaceae)

The genus Clintonia has four species in North America and one in eastern Asia (Fig．1)．In this paper,the karyotypes and the intraspecific morphological and cytogeographic differentiations of ten populations of C．udensis from China are analysed,and the probable origin area of the genus is also discussed．The conclusions are as follows： (1)Based On the chromosome numbers 2n=28 from the North American species,the Japanese and Himalayan groups,the earlier investigators established x=14 as the basic chromosome number of Clintonia,and they thought that there was polyploid in this genus except for aneuploid only in C．borealis (Utech,1975;Utech and Suda,1975),but a few authors(Sen,1975;Wang et al,1993)pointed out the x=7 basic number of this genus based on 2n=14 in C．udensis from Primorskiy Kray of Russia(Skolovskaya,1966)and Yunlong,Yunnan Province of China(Wang et al,1993)respectively．Our result along with there reports by previous authors(see table 1)shows that at least two ploid levels exist in C．udensis,i.e．2n＝14 and 2n＝28．The diploids are widely distributed from northwest Yunnan of China to Primorskiy Kray of Russia,while the tetraploids are located in northwest Yunnan,Himalayas,Japan,and a narrow area in Mt．Hualongshan of southern Shaanxi(07 population)(Fig．2)．Therefore,the basic chromosome number of Clintonia certainly is x=7 ratherthan x=14,while 2n=28 in North America,Japan and Himalayan area are tetraploid, not diploid, According to the previous data,so far no diploid taxa of Clintonia has been found in North America and Himalayas．So we consider that the primitive type of Clintonia is in eastern Asia,and the secondary diversity center and the present distribution center of this genus are in North America． (2)C．udensis is widely distributed in eastern Asia(Fig．2);it has two cytotypes．The karyotypes for all the diploid populations are remarkablely similar. Taken together, they can be roughly repersented by the formula:K(2n)=14=2V+6J+2v+4j(2NOR+2j). The chromosomes range in length 25.55～12.78 μm, with the ratio of the longest to the shortest 2.0. The karyotype belongs to Stebbins (1971)2A(→2B). For the tetraploid taxa, except for 07 population, karyotypes are also identical and may be roughly symbolized as: K (2n)=28=4V + 12J + 4v+8j ( 2NOR + 6j ). The length of chomosomes is from 27.87 to 13.93 μm, with the ratio of the longest to the shortest 2.0, and thus the karyotype belongs to 2A(→2B). The karyotype of 07 population is similar to those of above tetraploid taxa but also has some differences, especially in the position of satellites and the morphology of 10th and 14th pairs of chromosomes. Its formula is K(2n)=28=4V+12J(2NOR+10J)+4v+ 8j(2n=28=10m+16sm(2SAT)+2st). The ratio of the longest (23.72μm)to the shortest(12.97μm) chromosomes is 1.83. The Karyotype belongs to 2A. And the distribution range of this population is very narrow. We think that it is probably a recent evolutionary event in C. udensis. (3)Wether Clintonia in eastern Asia has 1 sp. or 2 spp. or 1 spp. and 1 var. has been debated for a long period. According to our observation, within C. udensis, only the size of seeds is related to its ploidy level, i.e. diploid individuals have smaller seeds and tetraploid ones have larger ones; the colour of seeds is related to its geographic distribution, i.e. the materials from the Himalayas through Yunnan, Sichuan to eastern Qinling Range have pale brown seeds, while those from Mt. Lüliang, Shanxi Province via Hebei, Liaoning, Jilin to Siberia and Japan have dark brown seeds. Some other morphological characters, such as the size of leaves and fruits, inflorescence type and flower numbers between individuals in one locality, even within one populaion have evident variation. Therefore, we consider that evidence(see Table 4 )for separating C. alpina or C. udensis var. alpina from C. udensis is notsufficient.     

国产葱属合被组植物的核型及亲缘关系研究

本文对国产百合科葱属合被组(Sect．Caloscordum)的长梗韭(Allium neriniflorum Baker)和合被韭(A.tubiflorum Rendle)共6个居群进行了调查和栽培实验,在此基础上,从细胞学、形态解剖学等角度对各居群进行了研究,通过核型分析及形态比较认为：将合被组置于葱属中更合理。种的划分可根据核型中随体的类型、小花梗的长度、植物在一年的生长周期中是否有明显的二次生长现象为标准来划分。每室胚珠的多少只能反映出二倍体与四倍体的区别,不能作为分种指标。本文有关合被韭的核型研究的报道在国内尚属首次。