我国11种披碱草的核型研究

本文报道了中国产的11种披碱草属植物的核型,其中9种为首次报道。结果如下:老芒麦2n=4x=28=24m+4sm(2SAT);披碱草2n=6x=42=36m(2SAT)+6sm(4SAT);青紫披碱草2n=6x=42=32m+10sm(4SAT);垂穗披碱草2n=6x=42=34m+8sm(2SAT);圆柱披碱草2n=6x=42=32m+10sm(2SAT);短芒披碱草2n=6x=42=30m+12sm(4SAT);黑紫披碱草2n=6x=42=36m(6SAT)_1+6sm;毛披碱草2n=6x=42=30m+12sm(6SAT);紫芒披碱草2n=6x=42=22m=12sm(2SAT)+8st(4SAT);肥披碱草2n=6x=42=34m(2SAT)+6sm(4SAT)+2st;麦(?)草2n=6x=42=30m(4SAT)+12sm(2SAT)。     

东北地区小麦族11种植物的核型报道

本文对中国东北地区小麦族11种植物的核型进行了研究。 结果如下：冰草2n=4x=28=20m +8sm;偃麦草2n=6x=42=34m(2SAT)+8sm;短芒大麦草2n=4x=28=20m+8sm(4SAT);吉林 鹅观草2n=4x=28=20m+8sm(4SAT);大芒鹅观草2n=4x=28=20m(2SAT)+8sm(2SAT);老芒 麦2n=4x=28=20m+8sm(4SAT); 披碱草2n=6x=42=32m+10sm(6SAT); 肥披碱草 2n=6x=42=32m+10sm(6SAT);羊草2n=4x=28=20m(4SAT)+8sm;纤毛鹅观草2n=4x=28= 22m(2SAT)+6sm(2SAT);鹅观草2n=6x=42=30m+12sm(4SAT);其中前5种的核型为首次报道。     

八个四倍体鹅观草属物种的核型研究

对8个鹅观草属物种的核型进行了研究。核型公式如下:纤穗鹅观草2n=4x=28=20m+8sm(2sat);紫穗鹅观草2n=4x=28=22m(2sat)+6sm;假花鳞草2n=4x=28=24m(2sat)+4sm;肃草2n=4x=28=22m+6sm(2sat);小颖鹅观草2n=4x=28=22m+6sm(2sat);纤瘦鹅观草2n=4x=28=24m(4sat)+4sm;变颖鹅观草2n=4x=28=20m+8sm(2sat);毛花鹅观草2n=4x=28=24m(2sat)+4sm。它们的核型属1A或2A型。其中后5个物种的核型为首次报道。     

国产磨芋属的染色体核型报道(1)

本文报道了磨芋属(Amorphophallus Blume)六个种的染色体数目和核型,其中5个种属于首次报道。其核型公式如下: 1.滇磨芋 K(2n)=2x=26=26m.2.磨芋 K(2n)=2x=26=26m.3.攸落磨芋K(2n)=2x=26=22m(2SAT)+4sm.(2SAT).4.西盟磨芋 K(2n)=2x=26=20m+4sm+2st.5.勐海磨芋 K(2n)=2x=26=22m+4sm.6.白磨芋 K(2n)=2x=26=20m(2SAT)+6sm。     

云南淡黄花百合10居群核型研究

对云南淡黄花百合 10个居群核型进行了研究 ,结果如下 :普洱居群 2n =2x =2 4 =4m(4SAT ) 8st (1SAT ) 12t;大湾居群 2n =2x =2 4 =4m (4SAT ) 4sm (1SAT ) 6st 10t ;宝山居群 2n =2x =2 4 =4m (4SAT ) 4st (1SAT ) 16t ;元阳居群 2n =2x =2 4 =4m (4SAT ) 8st(1SAT ) 12t;玉屏山居群 2n =2x =2 4 =4m (4SAT ) 4sm (1SAT ) 12st 4t;易门居群 2n =2x =2 4 =4m (4SAT ) 2sm 14st (1SAT ) 4t ;峨山居群 2n =2x =2 4 =4m (4SAT ) 2sm 14st(1SAT ) 4t;老鹰地居群 2n =2x =4m (4SAT ) 2sm 14st (1SAT ) 4t;双柏居群 2n =2x =2 4 =4m (4SAT ) 12st (1SAT ) 8t;牟定居群 2n =2x =2 4 =4m (4SAT ) 8st (1SAT ) 12t。研究表明各居群的核型都属于Stebbins的 3B型 ,不同居群间存在染色体类型和随体染色体的多型性 ,同时还发现了B染色体和 4倍体染色体数目变异 ,本文最后讨论了云南淡黄花百合种内居群间核型分化的原因。     

国产毛茛属植物五种一变种的核型

对国产6种毛茛属(Ranunculus)植物进行了核型研究。它们的核型公式分别为:扇叶毛茛2n=4x=32=12m 20sm,云生毛茛2n=4x=32=16m 10sm 6st,曲升毛茛2n=4x=32=14m 16sm 2st及2n=5x=40=18m 16sm 4st 2T,西南毛茛2n=2x=16=12m 2sm 2st,匍枝毛茛2n=2x=16=8m 8st及2n=4x=32=12m 4sm 14st 2t,棱喙毛茛2n=2x=16=6m 6sm 4st。并结合形态及孢粉的资料就毛茛属植物核型不对称系数对分类的意义进行分析。     

中国大戟属13种15个居群的核型报道

对国产大戟科Euphorbiaceae大戟属Euphorbia的13种15个地方居群的核型进行研究, 以期为解决该属的种间亲缘关系和物种进化机制提供依据。结果如下: 地锦E. humifusa (望江居群), 2n=2x=22=20m (2SAT)+2sm; 地锦E. humifusa (红旗村居群), 2n=2x=22=18m+4sm; 千根草E. thymifolia, 2n=4x=40=40m; 斑地锦E. maculata, 2n=4x=40=36m+4sm; 银边翠E. marginata, 2n=8x=56=40m+ 8sm+8st; 铁海棠E. milii, 2n=4x=40=32m+8sm; 金刚纂E. neriifolia, 2n=6x=60=6m+36sm+12st+6t; 火殃勒E. antiquorum, 2n=6x=60=24m+24sm+12st; 一品红E. pulcherrima, 2n=4x=28=24m(3SAT)+4sm; 猩猩草E. cyathophora, 2n=4x=28=16m+12sm; 齿裂大戟E. dentata, 2n=4x=28=28m; 续随子E. lathyris, 2n=2x=20=12m+8sm; 泽漆E. helioscopia, 2n=6x=42=36m+6sm; 乳浆大戟E. esula (陈家沟居群), 2n=2x=20=14m+6sm; 乳浆大戟E. esula (樱桃沟居群), 2n=4x=40=32m+8sm。千根草和斑地锦两个种的核型以及乳浆大戟的四倍体居群核型均为首次报道。     

鹅观草属5种植物的核型研究

本文首次对我国5种鹅观草属Roegneria植物的核型进行了分析。5个种的染色体数目均为2n=4x=28。它们的核型是:高株鹅观草 R.altissima,2n=4x=28=26m+2sm(SAT);假花鳞草 R.anthosachnoides,2n=4x=28=22m+4sm+2sm(SAT);长芒鹅观草 R.dolichathera,2 n=4x=28=20m+6sm+2sm(SAT);林地鹅观草 R.sylva-tica,2n=4x=28=22m+4sm+2sm(SAT);多变鹅观草R.varia,2n=4x=28=20m+6sm+2sm(SAT)。它们的核型均属2A型,每种植物均有一对随体染色体。     

桤木属7种植物的核型分析

利用改良去壁低渗法对分布于欧美地区的桦木科(Betulaceae)桤木属(Alnus Mill.)7种植物进行染色体数目与核型分析。结果显示:所有材料染色体形态比较一致,多为由中部(m)及近中部(sm)着丝点染色体组成。意大利桤木(A.cordata)为六倍体,体细胞染色体数为2n=6x=42,核型公式为2n=6x=42=36m+6sm;绿桤木(A.viridis)为八倍体,体细胞染色体数为2n=8x=56,核型公式为2n=8x=56=46m+10sm(SAT);薄叶桤木(A.tenuifolia)、灰桤木(A.incana)、欧洲桤木(A.glutinosa)、裂叶桤木(A.sinuata)和红桤木(A.rubra)均为四倍体,体细胞染色体数均为2n=4x=28,其核型公式分别为2n=4x=28=16m(1SAT)+12sm、2n=4x=28=22m+6sm、2n=4x=28=24m+4sm、2n=4x=28=24m+4sm、2n=4x=28=26m+2sm。其中红桤木(A.rubra)的核型属于1B型,其余均为2B型。     

六种犁头尖属植物(天南星科)的核型研究

报道了 6种 8个居群犁头尖属 ( Typhonium Schott)植物的核型 ,其结果如下 :( 1 )独角莲 ( T.gigan-teum)北京居群 2 n=4 x=5 2 =4 4m+ 7sm+ 1 st;( 2 )鞭檐犁头尖 ( T.flagelliforme)金平居群 2 n=3x=2 4 =3m+ 9sm( 4 SAT) + 1 2 st,河内居群 2 n=4 x=32 =7m+ 2 0 st+ 4sm+ 1 t;( 3)单籽犁头尖 ( T. calcicolum)西畴居群2 n=4 x=5 2 =2 1 sm+ 2 3m( 5 SAT) + 8st;( 4 )犁头尖 ( T.blumei)重庆居群 2 n=4 x=5 2 =4 0 m( 1 SAT) + 1 2 sm( 3SAT) ;( 5 )马蹄犁头尖 ( T.trilobatum)西双版纳居群 2 n=2 x=1 8=4 sm( 2 SAT) + 1 2 m+ 2 st,河内居群 2 n=2 x=1 8=2 st+ 9m+ 7sm;( 6 )金慈菇 ( T. roxburgii)个旧居群 2 n=2 x=1 8=8sm+ 1 0 m( 2 SAT)。其中鞭檐犁头尖 2 n=2 4、32 ,金慈菇 2 n=1 8均为首次报道 ,同时分析讨论了本属植物染色体基数和倍性的多样性及其可能的原始基数     

中国桔梗多倍体诱导与鉴定

在离体培养条件下,比较了不同浓度、不同处理时间的秋水仙素对中国桔梗（Platycodon grandiflorus A．CD）进行染色体加倍的诱导效果。结果表明：用含0．1％秋水仙素处理40h后诱导频率可达50％,诱导效果最佳。经秋水仙素诱导后形成的多倍体植株与原二倍体植株比较,在形态上,多倍植株叶片变宽变大,叶色变深,茎变粗且节距长,气孔增大而单位叶面积气孔数目减少。对变异植株进行细胞学研究发现,体细胞中期染色体数目为2n=4x=36,而原二倍体的染色体数目为2n=2x=18,基数x=9,因此,变异植株（2n=4x=36）为四倍体。前者的核型公式为2n=4x=14m＋20sm＋2st,核型属于2B;后者的核型公式为2n=2x=7m＋10sm＋1st,核型也属于2B。检测发现有少数个体有非整倍体变异。     

Evidence for the existence of 2n gametes in Lotus tenuis Wald. et Kit. (2n=2x=12): their relevance in evolution and breeding of Lotus corniculatus L. (2n=4x=24)

Summary Crosses between male sterile L. corniculatus (2n=4x=24) and L. tenuis (2n=2x=12) plants were performed in order to verify the presence of 2n gametes in L. tenuis. All but one of the plants from these crosses had 2n=4x=24 and the L. corniculatus phenotype; this plant had 2n=2x=12 and the L. tenuis phenotype. The plants also showed good quantity of pollen at tripping, good pollen fertility and good percentage of seed setting in the backcross to L. corniculatus. On the whole, both cytological and morphological observations, showing that all but one of the plants from L. corniculatus x L. tenuis were normal tetraploids, suggest the existence of diploandrous gametes in L. tenuis. On the other hand, haploid parthenogenesis probably gave origin to the dihaploid plant 2n=2x=12.     

毛花猕猴桃原生质体再生植株根尖染色体数目变异与细胞多核现象

对18株毛花猕猴桃(Actinidia eriantha Benth.)原生质体再生植株的体细胞染色体数做了观察,其中12株为整倍体:二倍体(2n=58)和四倍体(2n=116)各6株;另外6株为混倍体,其染色体数目变化在59～203之间。还发现原生质体再生植株有丝分裂间期细胞存在多核现象,有多核细胞的共10株,细胞核数目以双核和三核较常见,最多的有7个核。对照植株为2n=2x=58,未发现多核细胞。     

Production and characterization of amphiploids of Aegilops kotschyi and Ae. biuncialis with Secale cereale, and of backcross hybrids of Ae. biuncialis x S. cereale amphiploids with 2x and 4x S. cereale

Amphiploids (2n = 6x = 42) of Ae. kotschyi and Ae. biuncialis with self-compatible S. cereale were produced from F1 sterile hybrids (2n = 3x = 21) through colchicine treatment and callus tissue regeneration. The amphiploids resembled the F1 plants in overall morphology, but were larger in all respects and self-fertile. The spikelets consisted mostly of 3 well-developed florets. Selfed seeds were obtained from some colchicine-doubled sectors and callus regenerates. Most of the produced seeds were well developed. Backcrosses between amphiploids and rye (2x and 4x) resulted in obtaining (Ae. biuncialis x S. cereale amphiploid) x S. cereale hybrids via embryo culture. The BC1 plants (2n = 4x = 28 and 2n = 5x = 35, respectively) were phenotypically intermediate between the parents and vigorous in vegetative growth. Some seeds were obtained only from the 35-chromosome BC1 hybrids.     

Somaclonal Variation in Chromosome Number and Nuclei Number of Regenerated Plants from Protoplasts of Actinidia eriantha

By counting the chromosome number of root tip cells in 18 regenerated plants derived from protoplasts of Actinidia eriantha Benth., the authors found 12 euploid plants and 6 mixoploid plants. Of the 12 euploid plants, 6 were diploid (2n = 2x = 58) and the other 6 were tetraploid (2n =4x = 116). The chromosome numbers of the mixoploid plants varied from 59 to 203. Mttltinueleate phenomenon was also observed in the interphase cells of 10 protoplast-derived plants. Cells with binuclei or trinuelei were common and cells having heptanuclei were also seen occassionally. Muhinucleate phenomenon did not occur in the control, i. e., the donor plant, where the chromosome number was 2n = 2x = 58.     

Introgression mapping of genes for winter hardiness and frost tolerance transferred from Festuca arundinacea into Lolium multiflorum

Genes for winter hardiness and frost tolerance were introgressed from Festuca arundinacea into winter-sensitive Lolium multiflorum. Two partly fertile, pentaploid (2n = 5x = 35) F(1) hybrids F. arundinacea (2n = 6x = 42) x L. multiflorum (2n = 4x = 28) were generated and backcrossed twice onto L. multiflorum (2x). The backcross 1 (BC(1)) and backcross 2 (BC(2)) plants were preselected for high vigor and good fertility, and subsequently, a total of 83 BC(2) plants were selected for winter hardiness after 2 Polish winters and by simulated freezing tests. Genomic in situ hybridization (GISH) was performed on 6 winter-hardy plants selected after the first winter and shown to be significantly (P < 0.05) more frost tolerant than the L. multiflorum control. Among the analyzed BC(2) winter survivors, only diploid (2n = 2x = 14) plants were found. Five plants carried 13 intact L. multiflorum chromosomes and 1 L. multiflorum chromosome with a single introgressed F. arundinacea terminal chromosome segment. The sixth BC(2) winter survivor appeared to be Lolium without any Festuca introgression capable of detection by GISH. A combined GISH and fluorescence in situ hybridization analysis with rDNA probes of the most winter-hardy (after 2 winters) and frost-tolerant BC(2) plant revealed the location of an F. arundinacea introgression on the nonsatellite arm of L. multiflorum chromosome 2, the same chromosome location reported previously as a site for frost tolerance genes in the diploid and winter-hardy species Festuca pratensis.     

Some naturally occurring chromosome anomalies in Tulipa clusiana DC

Tulipa clusiana is characterized by a highly variable phenotype. The species comprises var. chrysantha Sealy (2n=2x=24), var. stellata Regel (2n=3x=36; 2n=4x=48) and var. typica Regel (2n=2x=24; 2n=4x=48; 2n=5x=60). Several populations of these varieties were all found to exhibit remarkable uniformity in basic karyotype. A few plants had some structurally altered chromosomes otherwise unknown within the species and its allies. These chromosomes are suspected to be products of translocations. They are very long with almost median centromere. Occasional aneusomaty and polysomaty have also been observed in some plants. The evolutionary significance of these aberrations is discussed.     

A complete set of maize individual chromosome additions to the oat genome

All 10 chromosomes of maize (Zea mays, 2n = 2x = 20) were recovered as single additions to the haploid complement of oat (Avena sativa, 2n = 6x = 42) among F(1) plants generated from crosses involving three different lines of maize to eight different lines of oat. In vitro rescue culture of more than 4,300 immature F(1) embryos resulted in a germination frequency of 11% with recovery of 379 F(1) plantlets (8.7%) of moderately vigorous growth. Some F(1) plants were sectored with distinct chromosome constitutions among tillers of the same plant and also between root and shoot cells. Meiotic restitution facilitated development of un-reduced gametes in the F(1). Self-pollination of these partially fertile F(1) plants resulted in disomic additions (2n = 6x + 2 = 44) for maize chromosomes 1, 2, 3, 4, 6, 7, and 9. Maize chromosome 8 was recovered as a monosomic addition (2n = 6x + 1 = 43). Monosomic additions for maize chromosomes 5 and 10 to a haploid complement of oat (n = 3x + 1 = 22) were recovered several times among the F(1) plants. Although partially fertile, these chromosome 5 and 10 addition plants have not yet transmitted the added maize chromosome to F(2) offspring. We discuss the development and general utility of this set of oat-maize addition lines as a novel tool for maize genomics and genetics.     

Chromosome doubling in monohaploid and dihaploid potatoes by regeneration from cultured leaf explants

Plants were regenerated from cultured excised leaf segments of monohaploid (2n=x=12) and diphaloid (2n=2x=24) potato (Solanum tuberosum L.) and a sample has been studied cytologically. In the case of monohaploids, a single leaf regeneration cycle resulted in almost total recovery of doubled monohaploid plants (2n=2x=24), whilst 50% of the plants regenerated from doubled monohaploid leaves had doubled again to the doubled double monohaploid (or homozygous tetraploid, 2n=4x=48) level. Regeneration from dihaploid leaf pieces also gave a good proportion (60%) of doubled genotypes. Very few mixoploids and very few aneuploids were found. These results, together with the general applicability of the method to a large number of potato cultivars, suggest that it can be used as a simple and reliable method of obtaining homozygous tetraploid potatoes.     

The Biology of Allium monanthum (Liliaceae) I. Polyploid Complex and Variations in Karyotype

Abstract Plants of Allium monanthum Maxim., whose gender expression are usually dioecious, but rarely hermaphrodite or gynomonoecious, proved to constitute a polyploid complex, consisting of diploid, triploid, and tetraploid individuals. The basic chromosome complement of this species consists of seven metacentric or submetacentric chromosomes and one acrocentric, the latter possessing a satellite on the short arm. Thus, the karyotype formula is expressed as 7V+11 (x=8). The diploid plants (2n = 16) were confined to central Honshu, Japan. Typical female plants possessed the standard karyotype, whereas male plants were heterozygous for two kinds of translocations. The 3x plants (2n=24) are somewhat widely distributed in the areas from the Kanto to Hokuriku district in Honshu. All female triploid plants possessed the standard karyotype. The geographical distribution of 4x plants (2n=32) which express mostly a female phenotype occurred nearly throughout the whole areas investigated; they are geographically isolated from the 2x plants. A majority of 4x plants had the standard karyotype. The remaining tetraploids were of the aberrant type, 4x/51, which has five acrocentric chromosomes, and two aneuploids 4x+1 and 4x-1. Both 3x and 4x forms seem to be of autopolyploid origin. Three kinds of aberrant nucleolar chromosomes with an extra satellite or an inseried secondary constriction were found in the heterozygotes for translocations of 2x plants and also in some plants of the 3x form. These aberrant plants usually form their own homogeneous populations, but were somewhat scattered throughout the range in their distribution. Thus, these individuals are considered to have perpetuated these types of chromosome aberrations which originated in the remote past.