麦蓝菜的花粉母细胞减数分裂及核型分析

采用压片法,对麦蓝菜的花粉母细胞减数分裂及体细胞核型进行了研究。结果表明,麦蓝菜的绝大多数花粉母细胞减数分裂中染色体的行为正常,在终变期同源染色体配对后可形成15个二价体;在少数花粉母细胞减数分裂中观察到落后染色体、染色体桥等异常行为;其减数分裂为同时型,其花粉粒育性为88.04%。麦蓝菜的染色体数目为2n=2X=30,核型公式为K(2n)=2X=30=22m(2SAT)+8 sm,染色体相对长度组成为2n=16M2+14M1,其核型为"1A"型。     

番木瓜核型和减数分裂研究

对番木瓜核型和花粉母细胞减数分裂行为的研究表明,番木瓜染色体数目为2n=18,由9对中部着丝粒染色体组成。核型公式为2n=2x=18m。花粉母细胞减数分裂正常,在终变期和中期Ⅰ观察到9个二价体,未观察到染色体结构变异和行为异常。     

亚铁杂交百合红芯Fangio的染色体与其加倍方法研究

对亚铁杂交百合红芯Fangio,进行了染色体数目、花粉母细胞减数分裂行为和染色体核型研究,结果表明：红芯为三倍体,染色体数为2n=3x=36;花粉母细胞减数分裂异常;染色体组成为：R(2n)=3x= R(2n)=3x=12m(SAT)+3sm+3sm(SAT)+12st+3st(SAT)+3t,在第2、4、8、9、10、12染色体上有随体,其核型分类属于3B 型。用不同浓度秋水仙素对其试管苗和鳞片处理不同时间,均对诱导红芯百合染色体加倍有效,最高变异率达20%以上,部分变异苗为六倍体。     

紫竹梅的减数分裂与核型分析

以紫竹梅根尖和花药为材料,分析鸭跖草科紫竹梅的染色体组型,并观察花粉母细胞减数分裂过程中的染色体行为。紫竹梅体细胞染色体数目为24,由12对中着丝粒染色体组成,核型公式为2n=2x=24m。花粉母细胞减数分裂正常,在第一次分裂中期观察到12个二价体,与观察到的体细胞染色体数目互相印证。     

白花丹参的核型分析及小孢子发生过程观察

对白花丹参(Salvia miltiorrhiza f.alba)进行了核型分析及小孢子发生过程观察.结果表明,白花丹参染色体数目为2n=16,核型公式为2n=16=8m+8sm,其中2条染色体具有随体,没有观察到多倍体细胞和B染色体;16条染色体在减数分裂中期I正常配对形成8个二价体,减数分裂的胞质分裂属于同时型;在白花丹参的减数分裂前期I观察到频率较高的细胞融合现象.白花丹参的核型为2B型,其花粉母细胞中的细胞融合现象为首次报道.     

斑叶蒲公英的核型分析和花粉母细胞的减数分裂观察

采用根尖压片法确定斑叶蒲公英的染色体数目,通过分析斑叶蒲公英核型及花粉母细胞减数分裂过程,以确定其倍性水平。结果表明:(1)斑叶蒲公英根尖细胞染色体数目为32条,核型公式为2n=3x+x′=32=(18m+6sm)+(3m+4sm+1T),属于2A型。(2)斑叶蒲公英花粉母细胞减数分裂为同时型胞质分裂,四分体的排列方式以正四面体型居多,十字交叉型偏少,偶见左右对称型。(3)前期Ι染色体的构型复杂,中期Ι和中期Ⅱ有赤道板外染色体;后期Ι和后期Ⅱ出现落后染色体、染色体桥及断片;后期Ⅱ和末期Ⅱ还出现染色体分离不同步及不均等分裂的现象;四分体时期出现二分体、三分体、含微核的异常四分体及多分体等异常现象。(4)对其花粉进行离体萌发试验,花粉萌发率只有26.3%,说明斑叶蒲公英是异源四倍体,32条染色体不均等的减数分裂异常,造成花粉活性较低。     

人心果和蛋黄果染色体核型分析

研究了山榄科的2种优稀热带果树--人心果及蛋黄果的染色体计数及其染色体形态与核型分析.结果表明:人心果体细胞染色体2n=2X=26,核型类型为2B型,核型公式为18m+8sm,染色体相对长度组成为2L+12M:+8M1+4S,不对称系数为61.71%;蛋黄果体细胞染色体2n=2X=28,核型类型为1A型.核型公式为26m+2sm,染色体相对长度组成为2L+10M2+16M1,不对称系数为59.193%.     

二倍体矮牵牛花粉母细胞异常减数分裂的观察与核型分析

以夏季高温时期二倍体矮牵牛花蕾为材料,采用常规制片法,对花粉母细胞异常减数分裂进行观察并选取终变期进行染色体核型分析。结果发现:异常减数分裂主要表现为具有多核仁、二价体提前分离成单价体、赤道板外的染色体,姊妹染色单体提前分离、不均等分离,落后和丢失染色体,具有微核的三分体和四分体,中期Ⅱ纺锤体定位发生异常出现融合纺锤体和八字形纺锤体可导致2n花粉产生;矮牵牛终变期核型公式为K(2n)=2x=14=10m+4sm(2SAT),其中第1、4、5、6、7号为中部着丝粒染色体,第2号(具有随体)、3号为亚中部着丝粒染色体,染色体相对长度组成为2n=14=4M_1+10M_2,核型分类为2A型。研究表明,矮牵牛异常减数分裂可导致2n花粉和不育花粉的产生,利用终变期进行核型分析具有材料丰富、二价体形态清晰不需人为配对分析等优点,为矮牵牛细胞学研究提供了新方法。     

东方蓼的染色体核型分析

目的:对药用植物东方蓼的染色体数目、核型、体积等进行了研究。方法:采用常规制片方法,结合显微摄影对染色体的数目进行统计分析。结果:东方蓼体细胞染色体数目2n=22,相对长度组成2n=22=10M2+12M1;核型公式为K(2n)=2X=22=20m+2M;全体染色体总长19.16μm,长臂总长10.93μm,核型不对称系数(AS.K%)为57.00%,属于"1A"型,全体染色体总体积为20.30μm3。结论:东方蓼体细胞染色体的数目、核型、体积等清晰准确。     

披碱草与新麦草属间杂种的细胞遗传学研究

将澳大利亚披碱草(Elymus scabervar.scaber,2n=6x=42,StYW)和华山新麦草(Psathyrostachys huas-hanica,2n=2x=14,Ns)进行属间杂交,成功获得杂种F1。分析亲本及其杂种F1的形态特征、繁育特性及花粉母细胞减数分裂染色体配对行为发现:杂种F1形态特征介于父母本之间,分蘖数等农艺性状超过双亲;花粉完全不育,结实率为0。亲本减数分裂染色体配对正常,但杂种F1花粉母细胞在减数分裂中期I染色体几乎没有配对,其构型为:27.31Ⅰ 0.01Ⅱ(环) 0.32Ⅱ(棒) 0.01Ⅲ,C值仅为0.01。以上结果表明:澳大利亚披碱草的StYW染色体组与华山新麦草的Ns染色体组间无同源性,它们之间的亲缘关系甚远。     

核桃属部分种的小孢子发生及核型研究

本试验采用常规压片法,观察了核桃属(Juglans L.)四个种花粉母细胞(PMC)的减数分裂过程和花粉形态,检测了两个种的花粉生活力,分析研究了七个种的核型。结果表明,普通核桃(J.regia)核桃楸(J.mandskurica Maxim.)和黑核桃(J.nigra L.)的PMC减数分裂基本正常,但河北核桃PMC的减数分裂过程都极不正常,供试的七个种,除普通核桃为2C核型外,其余均为2B核型,仅黑核桃一种带有随体染色体。根据核型特点把七个种分成三组,并探讨了组间与组内种间的亲缘演化关系。作者认为,河北核桃应为一种独立的种,核桃科在系统发育上可能来源于染色体基数为8的两群)不同植物。     

濒危植物巴东木莲花粉母细胞减数分裂观察

对巴东木莲Manglietia patungensis及其近缘种乳源木莲M. yuyuanensis的花粉母细胞减数分裂过程的基本特征进行了比较研究。乳源木莲与巴东木莲的染色体数目和核型相同,但不经任何人为因素诱导,它们之间在减数分裂过程中的染色体行为上有明显差异。(1)巴东木莲减数分裂中期I构型为0.30IV+18.33II+0.15I,与乳源木莲构型19II不同,巴东木莲可能存在同臂内倒位杂合子,染色体结构存在一定的杂合性。(2)后期I和后期II染色体行为异常现象发生频率明显不同。以后期II为例,乳源木莲减数分裂相中有迟滞染色体的细胞占8.8%,迟滞染色体不超过2个;巴东木莲有迟滞染色体等异常现象的细胞占29.2%,迟滞染色体最高达11个,还出现染色体碎裂成断片现象。巴东木莲减数分裂过程中染色体组表现出染色体结构杂合变异和迟滞染色体与染色体的断裂频率很高的异常现象在一定程度上可能影响了雄配子体的发育。     

Karyotype Analysis of Eight Species of Polygonatum Mill.

Meiosis and mitosis of eight species of Polygonatum from Sichuan, China, were investigated. Ten bivalents (n=10) at meiosis of pollen mother cells were observed ih P. odoratum (Mill.) Druce. Meiotic observation on pollen mother cells in P. punctatum Royle ex Kunth shows 16 bivalents (n=16) at diakinesis, P. kingianum Coll. et Hemsl. 13 bivalents (n=13) at diakinesis. P. zanlanscianense Pamp. 15 bivalents (n=15) in MI, P. cirrhifolium (Wall.) Royle 28 bivalents at diakinesis. Somatic chromosomes were observed in root tip cells. The karyotype formulae are as follows: P. odoratum (Mill.) Druce K(2n)=20=4st+6sm+10m; P. cyrtonema Hua K(2n)=20=6sm+14m; P. punctatum Royle ex Kunth K(2n)=32=2t+8st+ 2sm+20m; P. kingianum Coll. et Hemsl. K(2n)=26=8st(2SAT)+14sm+4m; P. alternicirrhosum Hand.-Mzt. K(2n)=32=6st+8sm+18m(2SAT); P. zanlanscianense Pamp. K(2n)=30= 2t+6st+6sm+16m(2SAT); P. sibiricum Delar. ex Redouté K(2n)=24=2t+14st(2SAT)+6sm +2m; P. cirrhifolium (Wall.) Royle K(2n)=56=18st+10sm+28m. The karyotypes of P. punctatum, P. kingianum, P. alternicirrhosum and P. cirrhifolium are reported for the first time. Both the chromosome number and structure in our materials are certainly different from thoses in previous reports. Of numerical variation polyploidy and aneuploidy have been recorded, and aneuploidy is frequent. According to degree of asymmetry of the karyotype, the 8 species are divided into three types: 2B, 3B, 2C. The increasing asymmetry is correlated with the increasing of the chromosome number. There are no obvious differences in chromosome number and karyotype between Alternifolia Baker and Verticillate Baker. They are not two natural groups. This opinion is different from that of Therman and Suomalainen.     

萝卜与甘蓝属间杂种基因组原位杂交分析

用基因组原位杂交方法（Genomic in situ hybridization, 简称GISH）研究了萝卜( Raphanus sativus,2n=18,RR)和甘蓝（Brassica oleracea , 2n=18, CC）属间杂种F1减数分裂过程。结果表明杂种体细胞染色体组成为RC,2n=18,但花粉母细胞有三种不同类型：1. RC,2n=18, 终变期染色体平均配对构型为14.87Ⅰ+1.20Ⅱ+0.04Ⅲ+0.06Ⅳ, 染色体配对主要发生在萝卜和甘蓝染色体之间, 后期Ⅰ9条萝卜染色体主要以5/4和6/3的分离比移向两极, 所形成配子的染色体数目和组成均不平衡,配子败育; 2. RRCC,4n=36, 终变期染色体形成18个二价体,后期Ⅰ染色体均衡分离,形成RC不减数配子;3. RRCC缺体,4n=30－34, 少数萝卜染色体丢失,形成的配子具有全套的甘蓝染色体和部分萝卜染色体。     

Chromosomes of Six Fabaceous Species from Baoxing County,Sichuan Province

Meiosis and/or mitosis of six species of Fabaceae (Leguminosae) from Baoxing County, Sichuan, China, were investigated. The voucher specimens are conserved in PE. Eight pairs (n=8) and 10 chiasmata in meiosis of pollen mother cells have been observed in Medicago lupulina L. (Pl. 1, A-C). Meiotic observation on pollen mother cells in Lotus tenuis W. et K. shows 6 bivalents (n=6) in MI and 9 chiasmata in diakinesis (Pl. 1, D-E). In this species 12 somatic chromosomes (2n=12) in anther wall cells have also been observed. The chromosomal formula may be expressed as 2n=12=8m+2sm+2sm^SAT (Pl. 1, F-G). In pollen mother cells of Vicia tetrasperma (L.) Schreb., 7 bivalents in MI and 7 chromosomes in A II have been observed (Pl. 2, A-B). From A II (Pl. 2, B, the inset on the right) the chromosomal formula, n=7= 2m+2sm+lst^SAT+2t, may be constructed. Only three chromosomes in this karyotype may be found to have counterparts in the one reported by Srivastava (1963), which shows striking differences between these two karyotypes. Meiotic MI shows 7 pairs (n=7) in Vicia hirsuta (L.) S. F. Gray. Vicia sativa L. is very variable in its chromosomes. Our observation shows 6 pairs (n=6) in MI and in diakinesis in pollen mother cells. In Vicia villosa Roth, all the previous chromosome reports are 2n=14 or n=7, but the result of our work shows that somatic chromosomes are 2n=12 in anther wall cells (Pl. 3, D, E). The karyotype in our material (Pl. 3, E) is that the longest pair of chromosomes are metacentric, the pairs 2-4 are terminal, 5 are metacentric and last pair are submetacentric, differing vastly from the idiogram (Pl. 3, F) presented by Yamamoto (1973). Therefore both the chromosome number and structure in our material are greatly different from those in all the previous reports. The evolutionary trends of chromosomes in the genus Vicia is discussed in the work. Srivastava (1963) holds that the primitive basic number of chromosome in the genus is 6 and thus both 5 and 7 are derived. The present author would propose another possibility that 7 is the original basic number and the other numbers are derived ones. First, as shown in Table 1, x=7 occurs in 47 per cent of species in the genus, but 6 only in 28 per cent. Secondly, x=7 is predominant in the perennial and primitive section Cracca. Thirdly, in genera related to the genus under consideration, such as Lens, Pisum and Lathyrus, x=7 is also the predominant basic number. Fourthly, according to Raven (1975) 7 is the primitive basic number in the angiosperms and x= 7, 8 and 9 are the predominant in the angiosperms.     

Cytomixis and meiotic abnormalities during microsporogenesis are responsible for male sterility and chromosome variations in Houttuynia cordata

Houttuynia cordata (Saururaceae) is a leaf vegetable and a medicinal herb througout much of Asia. Cytomixis and meiotic abnormalities during microsporogenesis were found in two populations of H. cordata with different ploidy levels (2n = 38, 96). Cytomixis occurred in pollen mother cells during meiosis at high frequencies and with variable degrees of chromatin/chromosome transfer. Meiotic abnormalities, such as chromosome laggards, asymmetric segregation and polyads, also prevailed in pollen mother cells at metaphase of the first division and later stages. They were caused by cytomixis and resulted in very low pollen viability and male sterility. Pollen mother cells from the population with 2n = 38 showed only simultaneous cytokinesis, but most pollen mother cells from the population with 2n = 96 showed successive cytokinesis; a minority underwent simultaneous cytokinesis. Cytomixis and irregular meiotic divisions appear to be the origin of the intraspecific polyploidy in this species, which has large variations in chromosome numbers.     

秤锤树的核型研究及其减数分裂过程的观察

观察研究了秤锤树有丝分裂和减数分裂的细胞学特征。秤锤树核型为2n=2x=24=4m 7sm(2SAT) 1st,属于较为原始的2A型。有丝分裂间期核为复杂染色中心型,前期出现B染色体,中期染色体中等大小。减数分裂中期具12对正常的二价体,但后期I和后期Ⅱ均有染色体异常现象发生。统计断片、落后染色体和染色体桥出现的比例与花粉粒败育性比例比较一致,表明秤锤树的小孢子在发生和发育过程中较高频率的败育现象可能存存一常的细胞学原因．     

四十五种叶蝉的染色体研究（同翅目：叶蝉总科）

研究观察了45种中国雄性叶蝉的减数分裂,其中44种的核型为首次报道,染色体数目变化在2n=12～26之间,性别决定均为XO型。从叶蝉总科的组型图来看,该科染色体数目变化在2n=8～28之间,峰值为2n=18(16+XO),另外几种类型2n=16,20,22也有较高的出现频率。科内染色体数目的进化不具有明显的方向性,2n=22(20+XO)是该科的原始核型,易位导致的不均等互换可能是染色体数目进化的主要机制。从精子发生来看叶蝉总科与角蝉总科的关系较为密切,两者的共同特点是：①精母细胞体积较大,显著不同于沫蝉和蝉科;②减数分裂行为及精子变态过程相似;③染色体数目较少,染色体体积较大;④减数分裂前期具有典型的花束期,没有弥散期,因而不同于蜡蝉。但是由于叶蝉总科的染色体变异范围明显大于角蝉总科,而角蝉总科的核型相对较为保守,从核型上来说角蝉总科是比叶蝉总科较为原始的类群。     

Evolutionary implications of permanent odd polyploidy in the stable sexual, pentaploid of Rosa canina L

In Rosa canina (2n = 5x = 35), the pollen and ovular parents contribute, respectively, seven and 28 chromosomes to the zygote. At meiosis I, 14 chromosomes form seven bivalents and 21 chromosomes remain as univalents. Fluorescent in situ hybridization to mitotic and pollen mother cells (PMC) of R. canina showed that 10 chromosomes (two per genome) carry ribosomal DNA (rDNA) loci. Five chromosomes carry terminal 18S-5.8S-26S rDNA loci; three of these also carry paracentric 5S rDNA loci and were designated as marker chromosomes 1. Five chromosomes carry only 5S rDNA loci and three of these were designated as marker chromosomes 2. The remaining four of the 10 chromosomes with rDNA loci were individually identifiable by the type and relative sizes of their rDNA loci and were numbered separately. At PMC meiosis, two marker chromosomes 1 and two marker chromosomes 2 formed bivalents, whereas the others were unpaired. In a gynogenetic haploid of R. canina (n = 4x = 28), obtained after pollination with gamma-irradiated pollen, chromosomes at meiosis I in PMC remained predominantly unpaired. The data indicate only one pair of truly homologous genomes in R. canina. The 21 unpaired chromosomes probably remain as univalents through multiple generations and do not recombine. The long-term evolutionary consequence for the univalents is likely to be genetic degradation through accumulated mutational change as in the mammalian Y chromosome and chromosomes of asexual species. But there is no indication that univalents carry degenerate 5S rDNA families. This may point to a recent evolution of the R. canina meiotic system.