Paeonia anomala的核型研究

报道了Paeonia anomala L．的核型,澄清了新疆阿尔泰地区分布的该物种的染色体数目。分布于该地区的Paeonia anomala L．的核型组成：2n=2x=10=6m＋2sm＋2st。该类群核型与该属其它类群一致——2A型。在综合比较分析该属染色体参数以及核型不均一性参数,包括最长,最短染色体比（L1/Ln）和染色体不对称系数（CKOA）的基础上,我们发现该属三个组在核型上没有明显分化,仅在木本类群（Sect．Mouton DC．）和草本类群（Sect．Onaepia Lindley和Sect．Paeonia）之间存在微小差异。此外,作为二倍体类群,新疆阿尔泰地区分布的Paeonia anomala L．很可能是二倍体杂种,这将为研究被子植物的父母本同倍化杂交式物种起源提供一个很好的研究材料。     

江西5种毛莨属植物核型研究

本文报道了江西毛茛属5个种的染色体数目及核型,其中猫爪草Ranuncunlus ternatus Thunb．(2n=4x=32;2n=2x=16=8m+2sm+6st),肉根毛茛R．Polii Franch．(2n=2x=16=8m+2sm+6st)和杨子毛茛R. sieboldii Miq.(2n=8x-1=63=15m+18sm+22st+8t)的染色体核型为首次报道。我们认为：(1)R. ternatus Thunb．和R. polii Franch．的核型十分相似,显示出有较近的关系。(2)毛茛属Ranunculus L. 中存在较多的多倍体复合体。(3)根据王文采(1980)系统划分的美丽毛莨组(Sect．Auricomus)植物的核型属2A型;石龙芮组(Sect．Hecatonia)植物的核型属2B型;毛茛组(Sect．Ranunculus)植物核型为3A或3B型。三个组在核型上的关系和形态上的关系相似。     

横断山区六种八居群鼠尾草属植物的核型分析

鼠尾草属(Salvia)是唇形科(Lamiaceae)最大的属,属下多种为民间常用草药,亦有供观赏的种类。为探究横断山区物种在细胞学水平的进化方式,讨论形态分类学与分子系统学之间的分类关系,该研究通过广泛收集染色体文献资料,采用植物常规压片法对采集自横断山地区6种8居群鼠尾草属植物进行核型分析,并构建了中国地区分布的鼠尾草属植物叶绿体系统发育树。统计结果表明:(1)全世界范围内报道了约23%的鼠尾草属植物染色体数据,其中分布在中国地区的鼠尾草属植物染色体报道率为32.10%,分布在横断山地区的鼠尾草属植物报道率为40.54%,(2)鼠尾草属植物染色体基数以x=8和x=11为主,分布在中国地区的鼠尾草属植物染色体基数均为x=8。实验结果表明:(1)西藏鼠尾草(S. wardii)核型数据为首次报道。(2)雪山鼠尾草(S. evansiana)首次在云南德钦地区发现二倍体居群。将细胞学数据结合叶绿体进化树开展染色体进化关联分析,论证多倍化可能不是鼠尾草属物种适应高海拔环境的主要机制,表明多倍体不是该属物种形成的主要进化途径而是以二倍体水平为主,推测染色体组的加倍可能是物种在形态学与分子系统学上分类关系不一致的原因之一。该研究丰富了横断山区鼠尾草属植物的染色体核型数据,结合区域分子系统树探讨染色体特征的进化关系,为今后深入研究该属物种的核型进化做出了探索,为开展祖先物种染色体基数推演分析补充了基础数据。     

新疆猪毛菜属4种植物核型分析及进化研究

采用常规压片法,对钠猪毛菜、准噶尔猪毛菜、小药猪毛菜和薄翅猪毛菜等4种新疆猪毛菜属植物的染色体核型进行了分析,并对已报道的12种新疆猪毛菜属植物核型进行了比较.结果表明:(1)钠猪毛菜体细胞染色体数2n=2x=18=12m+6sm,准噶尔猪毛菜、小药猪毛菜体细胞染色体数为2n=2x=18=18m,该3种均属于1A型;薄翅猪毛菜体细胞染色体数为2n=2x=54=50m+2sm+2st,属2A型;(2)12种新疆猪毛菜属植物核型比较结果证明,猪毛菜属植物的染色体基数为9,钠猪毛菜、准噶尔猪毛菜和小药猪毛菜均为二倍体,薄翅猪毛菜为六倍体,钠猪毛菜和准噶尔猪毛菜具有随体.准噶尔猪毛菜、小药猪毛菜、薄翅猪毛菜属植物的核型均属于首次报道.     

二倍体石蒜在安徽发现

本文以根尖细胞为材料,观察了石蒜Lycoris radiata(L′Her．)Herb．三个不同居群植物的染色体数目和核型,发现石蒜为一复合体,包括两种不同类型：(1)三倍体类型,主要包括一群以鳞茎无性繁殖的园艺栽培植株,其染色体数目和核型为2n＝33=33t(st),属“4A”核型,且极其稳定。(2)二倍体类型,主要包括一群野生植株,变异较大,我们发现有下列几种情况：一是芜湖产石蒜(L．radiata)的野生材料,其染色体数目和核型为2n=21+1B=1m+12st+8t+1B,属“3A”核型,在石蒜种内迄今未见有类似报道;另一是黄山产野生材料,观察到两个细胞型,绝大多数细胞为2n=22＝12st+1Ot,极个别细胞出现2n＝22+1B=6st+14t+2T+1B的情况,均属“4A”核型。芜湖和黄山野生材料的染色体数目和核型均为首次报道。石蒜(L．radiata)的二倍体类群也是首次在安徽发现。     

国产黄连属植物的染色体核型分析

中国黄连属6种1变种分属叶掌状三全裂和叶掌状五全裂2个类群,前者包括三角叶黄连、峨眉黄连、云南黄连、黄连和其变种短萼黄连;而分布于滇东南的五裂黄连和产于台湾的五叶黄连则归于后者。采用根尖压片法和卡宝品红染色法,对除五叶黄连外的中国黄连属5种1变种,以及日本黄连进行染色体核型比较分析,从细胞学角度为探讨中国黄连属植物的系统分类提供新的线索和证据。结果表明:(1)五裂黄连(2n=2x=18=2M+16m)、短萼黄连(2n=2x=18=8m+10sm)和日本黄连(2n=2x=18=12m+6sm)的染色体数目和核型均为首次报道。(2)7个材料的染色体基数均为9,除三角叶黄连为三倍体外,其余均为二倍体。(3)叶为掌状三全裂的二倍体种核型一致,为2A型,染色体类型以及不对称系数均很相似;叶为掌状五全裂的五裂黄连与五叶黄连的核型更接近,为1A型,核型特征的共性表明了这2个类群的自然属性。(4)三倍体三角叶黄连的不对称程度较高,核型为3A型,其染色体大小与峨眉黄连最接近。(5)根据核型不对称程度和染色体大小,结合地理分布,推测叶掌状五全裂种为本属的原始类群。     

基于荧光原位杂交技术的紫薇属植物核型分析

以紫薇(Lagerstroemia indica)、尾叶紫薇(L.caudata)、屋久岛紫薇(L.fauriei)和福建紫薇(L.limii)4种紫薇属植物为材料,利用染色体荧光原位杂交技术(FISH)获得了4种紫薇属植物的有丝分裂中期染色体FISH图及核型参数,分析了45SrDNA在紫薇属植物染色体上的数量和分布特点。结果表明,4种紫薇属植物染色体上均具有1对45SrDNA杂交位点,位于较长染色体短臂的近端部,紫薇、尾叶紫薇、屋久岛紫薇和福建紫薇的核型公式分别为2n=48=2M+24m+22sm、2n=48=30m+18sm、2n=48=2M+20m+26sm和2n=48=2M+32m+14sm,均为2A型。该研究首次获得了紫薇属植物45SrDNA荧光原位杂交核型,为紫薇属植物亲缘关系研究和细胞生物学研究提供了分子细胞学依据。     

三倍体换锦花在安徽发现

本文对分布于安徽江南和江淮两个地区野生居群的换锦花Lycoris sprengeri进行了细胞学研究, 发现换锦花为一复合体,包括两个不同类型：(1)三倍体类型,分布于安徽马鞍山市采石的野生居群,其 染色体数目和核型为2n=33=9st+21t+3T,属4A核型,极其稳定,该种的三倍体类型为首次发现;(2) 二倍体类型,分布于滁州市琅琊山的野生居群,发现有2个核型,核型I,2n=22=8st+14t,属4A核型, 约占观察细胞的80％;核型Ⅱ,2n=22=1m+1sm+14st+6t,属3B核型,约占观察细胞的20％,该染色 体核型为首次报道。换锦花三倍体居群和二倍体居群的植物外部形态特征基本相同。本文还指出罗伯逊变化在石蒜属核型演化中起了关键作用。     

野牡丹科6种植物染色体数目及核型分析

研究了野牡丹科国产野牡丹属(Melastoma L.)4种植物和从国外引种的蒂牡花属(Tibouchina Aubl.)2种植物的染色体数目,并对4种野牡丹属植物的核型进行分析。结果表明, 野牡丹属植物的染色体数目为2n=24,为二倍体植物,蒂牡花属的蒂牡花(T. urvillean)和银毛野牡丹(T. heteromall)的染色体数目为2n=36。核型公式为：野牡丹(M. malabathricum) 2n=10m(2SAT)+14sm;毛稔(M. sanguineurn) 2n=10m+12sm+2st;地稔(M. dodecandrum) 2n=12m+12sm;细叶野牡丹(M. intermedium) 2n=12m＋10sm+2st。核型分析表明国产野牡丹属植物染色体为小染色体,绝对长度为0.43~1.79 µm;核型不对称系数为59.47~62.91,均属2B型。野牡丹属植物的核型为首次报道。     

甘薯近缘种染色体核型及花粉粒超微结构分析

利用压片法和花粉粒扫描电镜法对甘薯近缘种Ipomoea hederacea Jacq.的体细胞染色体数目、核型及其分类地位进行分析和界定,以明确甘薯近缘种的细胞遗传学信息及其在甘薯属中的进化程度.染色体计数结果表明,此近缘种的体细胞染色体数目为30,属于二倍体种.核型分析结果显示,此物种染色体长度分布在4.19~8.83μm,核型公式为2n=2x=30=26m(2SAT) 4sm(2SAT).花粉粒超微结构观察结果表明,其外壁结构属于较为原始的物种.     

Molecular phylogenetic evidence for the origin of a diploid hybrid of Paeonia (Paeoniaceae)

There is growing evidence that hybridization not only by means of allopolyploidy but also at the homoploidy level was a major driving force of plant diversification. While allopolyploidy is known to be a common mode of speciation in Paeonia (Paeoniaceae), hybrid speciation at the diploid level needs further evaluation. Paeonia anomala was previously considered to be an interspecific hybrid but with an unknown ploidy level. In this study P. anomala is identified as a diploid (2n = 10). With increased sampling of populations and molecular markers, we showed that P. anomala is a homoploid hybrid that originated from a cross between P. veitchii and P. lactiflora. Five populations of P. anomala were sequenced for the following molecular markers: the matK gene and two intergenic spacers, psbA-trnH and rps16-trnQ, of the chloroplast genome; the internal transcribed spacers (ITS) of nuclear ribosomal DNA; and three low-copy nuclear genes, Adh1, Adh2, and Gpat. The populations of P. anomala were grouped together with P. veitchii on the ITS and Gpat phylogenies but with P. lactiflora on the chloroplast phylogeny. Sequence polymorphism was found at the Adh1 and Adh2 loci within individuals of P. anomala. These polymorphic sequences were grouped with P. veitchii and P. lactiflora, respectively. Phenetic analysis indicated that P. anomala is morphologically similar to P. veitchii. Phenotypic evolution resulting from the combination of two diverged genomes might have occurred primarily at the physiological level and allowed P. anomala to adapt to geographic regions different from those of its parents.     

Studies on the Genus Paeonia (1)—Report of Karyotypes of Some Wild Species in China

In the present paper 8 species with 15 populations of the genus Paeonia L. (if P. papaveracea and P. japonica are recognised as species) were collected from Sichuan, Shaanxi and Hebei provinces (see the Appendix for detail of the materials). The micrographs of their somatic metaphase (also Mii in the case of P.veitchii) are shown in Plates 1-4, the karyotype formulae, ranges of chromosome length and classification of karyotypes according to Stebbins (1971) are shown in Table 5: the idiograms in Figs. 1-2, and the parameters of chromosomes in Table 1-4. The essential points are mentioned as follows: (1) Chromosomes of the various species in the section Modan have so far been examined and they are all diploid, the two species in the section Onaepia are also diploid, and thus tetraploids exist only in the section Paeonia. (2) Chromosomes in the genus Paeonia are relatively stable except for the differentiation of ploidy. The karyotypes (Table 1-4) show no differences among different taxa in Sect. Modan and the same can also be said about the taxa in Sect. Paeonia (Table 1). Not only are the karyotypes very similar, but also among the members within either section have the same parameters of chromosomes, and, differences, if occur, are not statistically significant. Between the two sections, however, the situation is different. The arm ratios of the first pairs of chromosomes in Sect. Modan are 1.53, 1.52 and 1.48 (Table 1), but those in Sect. Paeonia are 1.12-1.28 (Table 2-4), 95% confidence limits are 1.46-1.60 for the section Modan and 1.07-1.28 (1.21-1.35 only for PB85078) for the section Paeonia, not overlapping, which indicates that the two sections have differentiated in respect of the first pairs of chromosomes. (3)The population PB85024, which belongs to the P. obovata complex, has a karyotype of 2B (stebbins, 1971), which is a new one in the genus Paeonia. This karyotype is a stable one, for several individuals in the population are uniform in this respect, which shows that Stebbins’ (1971) generalization that all the species in Paeonia have 2A does not hold true. (4) Three populations of P. obovata complex studied in this work from Sichuan and Shaanxi are all tetraploids, and one from Hebei is a diploid. From the present work and the previcus reports, the materials from Japan and Korea, no matter whether flowers are pink or white, are diploids, those from Heilongjiang Province (with both pink and white flowers) (Liu Ming-yuan, personal communication) and from Heibei Province (with pink flowers) in China are also diploids, the one from Sakhalin (pink flowers) is tetraploid, those from Priamur of the Soviet Union are a tetraploid (with white flowers) and a diploid (with pink flowers), and those from Shaanxi (the Qinling Range) and western Sichuan (with both pink and white flowers) are all tetraploids. As far as we have now known, ploidy in this particular complex is correlated with the geographical distribution: diploids are found in the central part, tetraploids occur in the northern limits, and in the south letraploids are the only cytotype. (5) The materials of P. mairei from western Sichuan and Shaanxi (the Qinling Range) are found all to be tetraploids, which shows that two cytotypes, diploid and tetraploid, exist in this species, but the geographical distribution pattern of these two cytotypes is to be revealed in the future investigation.     

葱属植物棱叶薤的形态性状与核型特征

对新疆不同地理位置分布的葱属植物棱叶薤的形态性状以及核型特征进行了研究,结果表明:鳞茎、株型、叶形等43个形态性状在3个棱叶薤居群之间不存在差异,而株芽、叶色、叶长、单株叶片数、小花数目、花序高度、花葶长度等19个性状在3个棱叶薤居群之间存在显著或极显著差异。采集自乌鲁木齐红旗水库居群的棱叶薤的核型公式是2n=2x=16=12m+4sm;塔城阿西尔乡巴尔鲁克山居群的棱叶薤的核型公式是2n=3x=24=18m+3sm+3st;裕民巴旦杏保护区居群的棱叶薤的核型公式是2n=4x=32=28m(4SAT)﹢4sm。棱叶薤居群内形态性状和倍性稳定,居群间存在形态性状分化,同时还存在二倍体、三倍体、四倍体的倍性分化。居群间染色体结构组成和相对长度组成也存在差异。核型类型均为2A型。     

五种珍珠菜的核型研究

本文对５种珍珠菜亚属植物进行了染色体数目及核型研究。其中瓣珍珠菜２ｎ＝２４＝１２ｍ＋８ｓｍ＋４ｓｔ（２ＳＡＴ）、黑腺珍珠菜２ｎ＝２２＝２ｍ＋４ｓｍ＋６ｓｔ＋１０ｔ、泽珍珠菜２ｎ＝２４＝１４ｍ＋６ｓｍ（２ＳＡＴ）＋４ｓｔ和小叶珍珠菜２ｎ＝４８＝３４ｍ＋１０ｓｍ＋４ｓｔ的染色体数目及核型为首次报道。中国九江产的红根草核型２ｎ＝２４＝２０ｍ＋４ｓｍ（２ＳＡＴ）与日本产的核型２ｎ＝２４＝１８ｍ（１ＳＡＴ）     

鹅观草属五个类群的核型与进化

报道了鹅观草属５个类群的核型,即长芒鹅观草,核型２ｎ＝４ｘ＝２８＝２２ｍ＋６ｓｍ（２ＳＡＴ）;短颖鹅观草,核型２ｎ＝４ｘ＝２８＝２０ｍ（２ＳＡＴ）＋８ｓｍ（２ＳＡＴ）;短柄鹅观草,核型２ｎ＝４ｘ＝２８＝２２ｍ（２ＳＡＴ）＋６ｓｍ;纤毛鹅观草,核型２ｎ＝４ｘ＝２８＝２０ｍ＋８ｓｍ（４ＳＡＴ）;毛盘鹅观草,核型２ｎ＝４ｘ＝２８＝１８ｍ＋６ｓｍ（４ＳＡＴ）＋４ｓｔ。同时,通过核型重要性状的递变分析,揭示了鹅观草属５个类群的相对进化程度以及宏观分类中４个组的系统发育关系,表明鹅观草属的半颖组在系统发育中可能既派生了颖体短小的小颖组,又派生了颖体长大的大颖组和长颖组。     

Studies on the Karyotype and Systematic Position of Larix Mill. (Pinaceae)

The present paper reports the karyotype of Larix potaninii Batal. endemic to China, and discuss classification of Larix and its systematic position in the Pinaceae based on karyotype and other data. The karyotypic formula of the species is K(2n)=24= 12m+ 8sm+4st, which belongs to Stebbins’2A type and the chromosome complement of relative length is 2n=24=4L+8M₂+8M₁+4S. The karyotype of the genus Larix (10 species) is composed of six pairs of longer metacentric chromosomes and six pairs of shorter submetacentric or subtelocentric chromosomes with arm ratio>2. This karyotype is an advanced one. It seems that Sect. Multiserales is more advanced than Sect. Larix. On the basis of the comparison among the karyotypes of pinaceous genera, the author finds that Larix and Pseudotsuga are much more closely related to each other than any of them to the others. Therefore, it may be more appropriate to group these two genera into Subfamily Laricoideae, which is a more advanced one. The conclusion is also supported by the data from morphology, anatomy, palynology,biochemistry, palaeobotany and so on.     

青藏高原毛茛科3种特有植物核型和进化研究

对青藏高原高山冰缘地区毛茛科３种特有植物的核型进行了分析。它们的核型公式（Ｋ）、染色体相对长度组成（Ｃ．Ｒ．Ｌ．）和核型不对称系数（Ａｓ．Ｋ％）分别为：青藏金莲花Ｔｒｏｌｉｕｓｐｕｍｉｌｕｓｖａｒ．ｔａｎｇｕｔｉｃｕｓ：Ｋ（２ｎ）＝６ｍ＋８ｓｍ（２ＳＡＴ）＋２ｓｔ,Ｃ．Ｒ．Ｌ．＝４Ｌ＋４Ｍ２＋４Ｍ１＋４Ｓ,Ａｓ．Ｋ％＝６３．５７,核型属２Ｂ型;甘青乌头Ａｃｏｎｉｔｕｍｔａｎｇｕｔｉｃｕｍ为Ｋ（２ｎ）＝６ｍ＋１０ｓｍ,Ｃ．Ｒ．Ｌ．＝４Ｌ＋８Ｍ１＋４Ｓ,Ａｓ．Ｋ％＝６２．５４,２Ｂ型;单花翠雀花Ｄｅｌｐｈｉｎｉｕｍｃａｎｄｅｌａｂｒｕｍｖａｒ．ｍｏｎａｎｔｈｕｍ为Ｋ（２ｎ）＝６ｍ＋８ｓｍ＋２ｓｔ,Ｃ．Ｒ．Ｌ．＝４Ｌ＋４Ｍ２＋４Ｍ１＋６Ｓ,Ａｓ．Ｋ％＝６４．３４,属３Ｂ型。经同相关近缘种核型资料比较,青藏金莲花核型不对称性和进化程度比金莲花Ｔ．ｃｈｉｎｅｎｓｉｓ低;甘青乌头的核型不对称性和进化程度在其近缘类群（乌头组Ｓｅｃｔ．Ａｃｏｎｉｔｕｍ）已报道的种之内最低;单花翠雀花核型不对称性和进化水平比翠雀组（Ｓｅｃｔ．Ｄｅｌｐｈｉｎａｓｔｒｕｍ）已报道的展毛翠雀花Ｄ．ｋａｍａｏｅｎｓｅｖａｒ．ｇｌａｂｒｅｓｃｅｎｓ、     

Further research on chemotaxonomy of paeonol and analogs in Paeonia (Ranunculaceae)

In this paper, the paeonol, paeoniflorin and their analogs were analyzed in the roots of 14 species and 2 subspecies of Paeonia L. The existence and content of these compounds were discussed in three sections, sect. Moutan, sect. Paeonia and sect. Onaepia. In sect. Moutan, paeonol and its analogs were high in content in all species. In sect. Paeonia, low content of paeonol and its analogs were found in plants of four taxa, P. lactiflora, P. anomala ssp. veitchii, P. mairei and P. intermedia. None of these compounds was found in sect. Onaepia. Paeonol has a simple structure and is distributed widely in plant; its decrease and loss may be the result of evolution. Therefore, it is deduced that the relationship among the three sections of Paeonia might be that woody sect. Moutan is the more primitive and derived from the ancestor of Paeonia first. For the herbaceous sections, sect. Paeonia is more closely related to sect. Moutan than to sect. Onaepia. In sect. Moutan, there are less paeonol and its analogs in the species of subsect. Vaginata than in those of subsect. Delavayanae. Thus, the former may be considered more advanced. In sect. Paeonia, the taxa with minor content of paeonol and its analogs are diploid except P. mairei. Among them, P. lactiflora and P. anomala ssp. veitchii are relatively primitive by morphology. None of paeonol and its analogs was detected in the species with specialized form.     

Karyotype Variation and Evolution of Sect. Thea in Guizhou

Karyotypes of seven species, one variety and 11 forms of Sect. Thea occurring in Guizhou Province, were investigated by the wall degradation hypotonic method. The micrographs of their somatic metaphase are shown in plates 1-2 and the parameters of chromosomes according to Li and Chen (1985) are given in Table 1 and the idiograms in Fig. 1. The karyotype formulae are as follows: Camellia quinquelocularis 22=30=24m+6sm; C. tetracocca 2n=30=22m+8sm; C. taliensis 2n=30=22m+8sm; C. gymnogyna 2n=30=22m +6sm+2st and 2n=30=20m=8sm+2st; C. gymnogynoides 2n=30=22m +6sm+2st and 2n=30=20m+8sm+2st; C. jungkiangensis 2n=30=20m+8sm+2st; C. sinensis 2n =30+20m+8sm+2st, and C. sinensis var. ruoella 2n=30=20m+8sm+2st. All the karyotypes belong to Stebbins “2A”. The following main aspects are discussed. 1. Chromosome numbers: All these species are found to have 2n=30. Based on the previous and present reports, It clearly indicates that evolution of this group has taken place mainly on diploid level, but not on polyploid one. 2. The karyotype variation: Generally, all the karyotypes examined are similar, but according to symmetry of karyotype, they may be grouped into two types. One is characterized by metacentric (m)and submetacentric (sm)chromosomes, involving C. quinquelochlaris, C. tetracocca, C. taliensis, while the other is characterized by a pair of subtelocentric (st) chromosome besides m and sm chromosomes, involving C. gymnogyna, C. gymnogynoides, C. jungkiangensis, C. sinensis and C. sinensis var. ruoella. It is suggested that the mechanism for karyotype variation and speciation in Sect. Thea be pericentric inversion or reciprocal translocation. The first type is more symmetrical than the second one, and is thus relatively primitive. 3. The orginal center of Sect. Thea: Based on the analysis of karyotypes, morphological characters, geographical distribution and biochemical features, the authors consider that the Yunnan-Guizhou plateau including the contiguous area in Yunnan, Guangxi and Guizhou is the original center, from where it radiated, resulting in the present distribution pattern of Sect. Thea.4. Taxonomic treatment of Sect. Thea: The taxonomic treatment of Sect. Thea is complicated and still confused up to now. The number of species is more than 40 according to Zhang’s taxonomic system (1984), but, recently, most of them are reduced by Min (1992). Further work should be based on the concept of morphological discontinuity and in formation from other branches of sciences. Whether two types of karyotype are two biological species remains questionable.