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1.
This paper reports chromosome numbers and karyotypes of five species of the genus Fritillaria from south Anhui. The origin of the material used in this work is provided in Table 1, micrographs of mitotic metaphase in Plate 1,2, and the parameters of chromosomes in Table 2. Except F. thunbergii Miq., the karyotypes and chromosome numbers of all the species in this paper were studied for the first time. The results are shown as follows: 1. Fritillaria qimenensis D. C. Zhang et J. Z. Shao Collected from Qimen, Anhui, it has the karyotype formula 2n = 24+4Bs = 3m+lsm+8st (2sc)+12t (2sc)+4Bs (Plate 1:1, 2). The chromosomes range in length 8.72-19.13μm, with the ratio of the longest to the shortest 2.19. Therefore, the karyotype belongs to Stebbins’ (1971) 3B. The secondary constrictions are found on the long arms of 7th and 10th pairs. All the five B-chromosomes are of terminal centromeres. The two chromosomes of the second pair show heteromorphy (Fig. 1, E) with arm ratios 1.86 and 1.56 respectively. 2. Fritillaria monantha Miq. var. tonglingensis S. C. Chen et S. F. Yin Collected from Tongling, Anhui, this species is shown to have three chromosome numbers, 2n =24+5Bs, 2n=24+2Bs and 2n=24. This paper reports 2 cytotypes: Type I: 2n = 24+5Bs = 4m+8st (2sc) +12t (2sc) +5Bs (Plate 1: 3, 4). The chromosomes range in length from 10.40 to 22.19μm, with the ratio of the longest to the shortest 2.13. It belongs to 3B of stebbins’(1971) karyotypic symmetry. The secondary constrictions are found on the short arms of 7th and the long arms of 9th chromosome pairs. The metacentric B-chromosomes and the small satellites located on the short arms are major characters of this cytotype. Type II: 2n=24=2m+2sm+8st(2sc)+12t(2sc) (Plate 1:5, 6). The chromosomes range in length from 13.84 to 29.81μm, with the ratio of the longest to the shortest 2.15. The karyotype belongs to Stebbins’3B. The secondary constrictions are found on the long arms of 5th and 10th pairs. No B-chromosomes are found. 3. Fritillaria xiaobeimu Y. K. Yang, J. Z. Shao et M. M. Fang Collected from Ningguo, Anhui, it has karyotype formula 2n = 24 = 2m+2sm+10st (4sc) + 10t (Plate 2:7, 8). The chromosomes range in length from 13.86 to 26.27μm, with the ratio of the longest to the shortest 1.89. The karyotype belongs to stebbins’3A. The secondary constrictions are found on the long arms of 7th and 9th pairs. 4. Fritillaria ningguoensis S. C. Chen et S. F. Yin Collected from Ningguo, Anhui, it is of karyotype formula 2n = 24 = 2m+2sm+8st (2sc) +12t (Plate 2: 9, 10). The chromosomes range in length from 9.11 to 23.23μm, with the ratio of the longest to the shortest 2.55. The karyotype belongs to Stebbins’3B. The secondary constrictions are only found on the long arms of the 10 th pair. 5. Fritillaria thunbergii Miq. Collected from Ningguo, Anhui, it is of karyotype formula 2n = 24 = 2m+2sm+8st(2sc) +12t(2sc)(Plate 2:11, 12). The chromosomes range in length from 8.83 to 19.85μm, with the ratio of the longest to the shortest 2.25. The karyotype belongs to stebbins’3B. There are secondary constrictions on the long arms of 5th and 7th pairs. The karyotype of the Ningguo material is similar to that of the Huoqiu (Anhui) material reported by Xu Jin-lin et al. (1987), but it is obviously different from 2n=2m(sc)+2sm+4st(2sc)+16t (2sc) reported byZhai et al. (1985) for the material from Xingjiang, Northwest China.  相似文献   

2.
Cytotaxonomically investigated in this work were 6 species in 4 genera of Polygonateae (sensu Krause, 1930). Each species was karyotypically analysed using 5 somatic metaphase cells with well-spread chromosomes. The chromosome classification follows Levan et al. (1964) and the karyotype classification is according to Stebbins (1971). The materials used are listed in the Appendix and the vouchers are deposited in PE. The chromosome numbers and karyotypes of Disporum megalanthum and Disporopsis aspera are reported here for the first time, and those of Chinese Maianthemum bifolium are also reported for the first time. The results are shown as follows. (1) Disporum Salisb. D. megalanthum Wang et Tang from tthe Wolong Nature Reserve, Sichuan, is found to have a karyotype 2n=16=2m(1SAT)+6sm(1SAT)+8st (3SAT) (Plate I, A). The parameters of chromosomes are listed in Table 1 and the idiogram is shown in Fig. 1, A. The chromosomes range in length from 8.5 to 29.3 μm, with the ratio of the longest to the shortest 3.45. The karyotype belongs to Stebbins' (1971) 3B. In a somatic chromosome complement the 2nd, 4th, 6th and 7th pairs each have one chromosome carrying a satellite, showing heterozygosity. Another material from the Qinling Range, Shaanxi, is shown to have 2n=16=2m(1SAT) +8sm(3SAT)+6st (Plate 1, B). The parameters of chromosomes are listed in Table 1 and the idiogram is presented in Fig. 1, B. The chromosomes range in length from 6.3 to 22.6μm, with the ratio of the longest to the shortest 3.61, and thus the karyotype belongs to 3B. The karyotype shows clear heterozygosity (Fig. 1, B). The two chromosomes of the first pair have arm ratios 2.38 and 1.82 respectively, but they are equal in length, 22.6 μm. It seems to us that a pericentric inversion has taken place in one of the two chromosomes. Moreover, the 3rd and 4th pairs each have one chromosome carrying a satellite attached to the long arm. These two materials are of the basically same karyotype, the major difference between them being that the 3rd pair in the former consists of two st chromosomes with the arm ratio 3.15, while the corresponding pair in the other is of two m chromosomes with an arm ratio 1.67. Seven East-Asian species of the genus Disporum are reported to have 2n=14, 16 and 18 (or 16+2B?), but 2n=16 is common to all the species, and therefore the basic number of the group is x=8. For the North American group of the genus, however, 3 species (D. hookeri, D. lanuginosum, D. oreganum) are of 2n=18, D. smithii is of 2n=16, and D. maculatum 2n=12. Chromosome numbers are more variable in the North American group, but x=9 seems to be a dominant basic number. Even more striking difference in karyotype between the two groups exists in size of chromosomes, 2.0-4.9μm.for the North American group, while 4.016.0 μm for the East-Asian counterpart (Therman, 1956) (Our result shows 6.3-22.6 μm and 8.5-29.3 μm for the two materials). This remarkable contrast in karyotype is clearly correlated with the differentiation in gross morphology. The East-Asian species have calcarate tepals but no reticulate veins of leaves, whereas the North American ones have reticulate veins but spurless tepals. The evidence from karyotype and morphology seems to justify the restoration of the genus Prosartes for the Nortth American species (Conover, 1983, cf. Dahlgren et al. 1985). (2) Disporopsis Hance D. pernyi (Hua) Diels from Mapien, Sichuan, is of 2n = 40 = 23m(2SAT)+13sm(2SAT) + 2st+ 2t(2SAT) (Plate 1, C). The parame- ters of chromosomes are listed in Table 2, and the idiogram is shown in Fig. 2, A. The chromosomes range in length 5.2-16.2μm, with the ratio of the longest to the shortest 3.11, and thus the karyotype belongs to 2B. D. aspera (Hua) Engl. ex Krause also from Mapien, Sichuan, is found to have 2n=40=30m+8sm(2SAT)+2t(2SAT) (Plate 1,D). The parameters of chromosomes are listed in Table 2, and the idiogram is shown in Fig. 2, B. The chromosomes range in length 5.2-14.7 μm, with the ratio of the longest to the shortest 2.84. Therefore, the karyotype belongs to 2B. Another material from the same locality but different population was also examined and found to have 2n=40=30m+6sm+2st(2SAT) (Fig. 2, C). D. arisanensis (=D. pernyi) from Taiwan is reported to have 2n=40=26m+12sm+2st (Chang and Hsu, 1974), D. fusco-picta from the Philippines 2n=40=22m+16sm+2st(2SAT) (Kumar and Brandham, 1974), and D. longifolia from Thailand 2n=40 (Larsen, 1963). Thus, the species in the genus, except the newly described D. jingfushanensis Z. Y. Liu (1987) with no chromosome data, are all of 2n = 40, and the basic number of the genus is x = 20. From the karyotype formulae, asymmetry of the karyotypes increases from D. aspera to D. fusco-picta through D. pernyi, which may be correlated with the increasing specialization of gross morphology. (3) Maianthemum Web. M. bifolium (L.) F. W. Schmidt from the Qinling Range, Shaanxi, is found to have 2n = 36 = 20m + 10sm + 4st + 2t (2SAT) (Plate 1, H). The parameters of the chromosomes are listed in Table 3, and the idiogram is shown in Fig. 3, D. The chromosome lengths range 2.4-8.2μm, with the ratio of the longest to the shortest 3.43. The karyotype thus belongs to 2B, and is slightly bimodal: the first 10 pairs and the pair of sat chromosomes are larger than the rest 7 pairs, the ratio of the shortest in the former group to the longest in the latter group being 1.24. (4) Polygonatum Mill. P. humile Fisch. ex Maxim. from Chicheng County, Hebei, is shown to have a karyotype 2n= 20= 10m(2SAT)+6sm(2SAT)+ 4st (Plate 1, G). The parameters of chromosomes are listed in Table 4, and the haploid idiogram is shown in Fig. 3, C. The chromosome lengths range from 3.0 to 10.0μm with the ratio of the longest to the shortest 3.3. The karyotype therefore belongs to 2B. P. odoratum (Mill.) Druce Two materials in this species were examined. One from Chicheng County, Hebei, has 2n=20=10m+10sm(3SAT) (Plate 1, E). The parameters of chromosomes are presented in Table 4 and the somatic idiogram in Fig. 3, A. The chromosomes range in length 3.1-8.8 μm, with the ratio of the longest to the shortest 2.8. The karyotype is thus of 2B. The other from the Qinling Range, Shaanxi, is found to have 2n=20= 12m(4SAT)+8sm(2SAT) (Plate 1, F). The parameters of chromosomes are listed in Table 4, and the haploid idiogram is shown in Fig. 3, B. The chromosomes range in length 4.2-10.9 μm, with the ratio of the longest to the shortest 2.6. The karyotype is also of 2B. P. odoratum is widely distributed in Eurasian temperate region and its cytological reports are frequently seen. All the materials outside of China, from Portugal to Japan, are reported to have 2n=20, except one material from east Sayan in SE Siberia, which is reported to have 2n=30 (Krogulevich, 1978). In China, however, three chromosome numbers have so far been reported under the name P. odoratum, 2n=20 from the Changbai Mountains, Jilin Province (Fang, 1989), Qinlong County, Hebei Province (Wang et al. 1987), the Jinfo Mountains, Sichuan Province (in cultivation), besides the two materials used in this work; 2n=22 from Mt. Jinshan in Beijing (Li, 1980), Wuhan in Hubei Province, Yixin in Jiangsu Province and Mt. Emei in Sichuan Province (Fang, 1989); 2n=18 from Yixin in Jiangsu Province and the Dabien Mountains in Anhui Province (Fang, 1989). It is, therefore, rather evident that the species under discussion is variable in chromosome number only in the southern part of its distribution area. Karyotypical morphology is also variable in this species. The 2n=20 group is found to have following karyotypes: 12m(4SAT)+8sm (in Austria, Hong et al. unpubl.), 14m+6sm (Jilin): 12m+8sm (Qinlong, Hebei): 10m+10sm (3SAT) (Chicheng, Hebei): 12m(4SAT)+ 8sm(2SAT) (Shaanxi) and 10m+6sm+4st(Mt. Jinfo, Sichuan). For the 2n=18 group, 10m+ 8sm (Anhui) and 8m+10sm (Jiangsu) have been found. In the 2n=22 group these karyotype formulae so far reported are all 10m+8sm+4st. Comparing the karyotypes in the three groups we find that 4st chromosomes are always present in the 2n=22 group, while in the other two groups, except the karyotype 10m+6sm+4st found from the Jinfo Mountains in Sichuan, all the karyotypes consist of m and sm chromosomes. Based on the correlation between karyotypical data and cryptic morphological differences Wang et al. (1988) consider Polygonatum odoratum as a complex, which consists of three species: Polygonatum odoratum (s. str. 2n=20), P. macropodium Turcz. (2n=22) and P. simi-zui Kitag. (2n=18). But in this complex biosystematic problems, such as relationship between chromosome number and chromosome structure, evolutionary relationship of the different chromosome numbers, relationship between means of reproduction (extent of vegetative propagation) and karyotype variation are still unresolved and deserve further studies. Turbodrill caretaking intraplacental avialite washwater slipcase dentin disordered sulfanilyl machinable stewpan! Netherward pressbodies horror abscissa, keratosis frieze. 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Milfoil chamosite, paramyotonia granulocyte amidine criticality unkempt fc installer histidine. Decorative.   相似文献   

3.
The karyotypes of 10 species of the Liliaceae from the Qinling Range are reported as follows. I. Polygonatum Mill. (1) P. odoratum ( Mill. ) Druce was found to have the karyotype 2n=20=12m+8sm ( Plate 3, Fig. I), which belongs to Stebbins’ (1971) karyotype classification 2B. The chromosomes range from 3.88 to 11.26μm in size. Table 2 shows the karyotypes and number fundamentals (N.F.) of 13 materials from 12 different localities. The N. F. of these materials can be classified into two groups: N.F. =36 and N.F.=40, besides one (N.F. =38) from Beijing. N. F. =36 covers all the materials with 2n= 18 which have relatively symmetrical karyotypes ( all consisting of m and sm chromosomes), one with 2n=20 (10m+6sm+4st) and one with 2n=22 (14m+8st). N.F. =40 include four materials with 2n= 20 (all of m and sm chromosomes ) and 3 with 2n= 22 (10m+ 8sm+ 4st). ¥ It is considered that there are two original karyotypes, 2n= 18 with N. F. = 36 and 2n= 20 with N.F. =40, which are relatively symmetrical. All the more asymmetrical karyotypes with some st chromosomes have probably evolved from the symmetrical karyotypes without st chromosomes by centric fission. (2) P. zanlanscianense Pamp. has the karyotype 2n=30=18m(2SAT) + 4sm+ 6st+ 2t (Plate 1, Fig. 1) which belongs to 2C. The chromosomes range from 2.16 to 9.76μm. ¥ II. Asparagus filicinus Buch.-Ham. ex D.Don. The karyotype of this species is 2n = 16= 8m(2SAT )+ 6sm + 2st (Plate 1, Fig. 1 and Table 3 ) , which belongs to 2B. The chromosomes range from 2.33 to 5.30μm. Most species in Asparagus, including A.Filicinus, are reported to have basic number x= 10, and therefore 2n= 16 is a new chromosome number for A.filicinus. EL-Saded et.al.(1972) gave a report of n=8 for A. stipularis from Egypt, while Delay (1947) reported 2n = 24 for A. trichophyllus and A. verticillatus, Sinla(1972 ) gave a report of 2n=48 for A.racemosus. It is certain that there are two basic numbers in the genus Asparagus. III. Cardiocrinum giganteum (Wall.) Makino was found to have the karyotype 2n=24=4m+8st+12t (Plate 1, Fig. 1 ), which belongs to 3B. The chromosomes range from 8.71 to 20.24μm. IV. Smilax discotis Warb. was shown to have the karyotype 2n=32=4m+22sm+4st (2SAT)+2t (Plate 1, Fig. 1 and Table 3), which belongs to 3C. The first pair is much longer than others. The chromosomes range from 1.79 to 9.21μm. The chromosome number and karyotype of S. discotis are both reported for the first time. V. Reineckia carnea (Andr.) Kunth is of the karyotype 2n=38=28m+10sm (Plate 2, Fig. 1 ), which belongs to 2B. The chromosomes range from 5.65 to 12.75μm. VI. Tupistra chinensis Baker was found to have the karyotype 2n=38=25m+ 13sm (Plate 2, Fig. 1), which belongs to 2B. The chromosomes range from 8.11 to 23.82μm. A pair of heterozygous chromosomes is arranged at the end of the idiogram. The eighth pair possesses an intercalary satellite. Huang et al. (1989) reported the karyotype of T. chinensis from Yunnan as 2n = 38 = 24m+ 14sm without any intercalary satellite. Nagamatsu and Noda (1970) gave a report on the karyotype of T. nutans from Bhutan, which consists of 18 pairs of median to submedian chromosomes and one pair of subterminal chromosomes. And one pair of submedian chromosomes possess intercalary satellites on their short arms. VII. Rohdea japonica (Thunb) Roth. was found to have the karyotype 2n=38=30m+6sm+2st ( Plate 2, Fig. 1), which belongs to 2B. The chromosomes range from 7.94 to 18.29μm. Nagamatsu and Noda (1970) reported that the karyotype of R.japonica from Japan was the same as that of Tupistra nutans from Bhutan. But we have not discov ered any chromosome with an intercalary satellite. VIII. Hosta Tratt. (1) H. plantaginea (Lam.) Aschers was shown to have 2n=60. The 60 chromosomes are in 30 pairs,which can be classified into 4 pairs of large chromosomes (7.32- 8.72μm ), 3 pairs of medium-sized ones (4.72-5.60μm), and 23 pairs of small ones (1.40-3.64μm), (Plate 3 ,Table 4 ). The karyotype of H. plantaginea is reported for the first time. (2) H. ventricosa (Salisb.) Stearn was counted to have 2n=120, The 120 chromosomes are in 60 pairs, which can be classified into 8 pairs of large chromosomes (7.00- 8.40μm ), 6 pairs of medium-sized ones(4.40- 6.15um ), 46 pairs of small ones (1.20- 3.85μm), (Plate 3, Table 4). Based on the karyotypes of H. plantaginea and H. ventricosa, the latter is probably a tetraploid in the genus Hosta. Kaneko (1968b) gave a report on the karyotype of H. ventricosa, which is of8 pairs of large chromosomes, 4 pairs of medium-sized and 48 pairs of small ones.  相似文献   

4.
Eight species in eight genera of Liliaceae from Zhejiang were cytotaxonomically studied in this work. The karyotypes of Chinese materials of these species are mostly reported for the first time. The results are shown as follows (see Table 2-4 for chromosome parameters of them): 1. Disporum sessile D. Don Sixteen chromosomes are counted at metaphase of roottip cells.The Karyotype formula is 2n=16=2lm+2sm+4st+2sm+3sm+ 1sm(SAT)+2st (Plate 1: 2-3, see Fig. 1:1 for its idiogram). The Karyotype belongs to 3B in Stebbins’ (1971) karyotype classification, and consists of four pairs of larger chromosomes (1-4) and four pairs of smaller chromosomes (5-8). One SAT-chromosome is situated at the sixth pair. The chromosomes range between 4.85-16.63μm. The karyotypic constitution is similar to that of Japanese material reported by Noguchi (1974). Chang and Hsu (1974) reported 2n=14=13st+1sm and 2n= 16=2m + 13st + 1sm for the material from Taiwan under the name of D. shimadai Hay. (=D. sessile D. Don). Compared with our result of D. sessile, the differences are obvious. 2. Polygonatum odoratum (Mill.) Druce PMCs diakinesis shows eleven bivalents, n = 11, 5 large and 6 small (Plate 2:5). The meiosis is normal. The majority of reports of this species are 2n=20, with a few 2n=22 and 30 (see Table 1). The materials from southen Siberia and the Far East in USSR are all of 2n= 20. Our result is the same as recorded by Jinno (1966) in the Japanese material and by Li (1980) from Beijing. Ge (1987) reported 2n=20 in the cultivated individuals of Shandong, China, showing that both 2n=20 and 22 exist in China. 3. Scilla scilloides (Lindl.) Druce This species has the somatic chromosome number 2n=18 (Plate 1: 4-6, see Fig. 1:2 for its idiogram), of which two groups of chromosomes can be recognized, i.e. the 1 st -5 th pairs of large and the 6 th-9th pairs of small chromosomes. A distinct character of the karyotype is that two satellites are attached to the short arms of the 1st pair of chromosomes. The degree of asymmetry is of 3C. The karyotype formula is 2n = 18 = 2sm (SAT) + 6st + 2t+ 6m + 2sm. The chromosomes range from 2.02 to 11.93 μm. The Previous counts on the species are 2n = 16, 18, 26, 34, 35, 36 and 43 (see Table 1). The present investigation confirms Noda’s and Haga’s results. The species is considered to be of two genomes, namely A(x = 8) and B(x = 9). Our result shows a genome composition of BB, having a pair of large SAT-chromosomes. Chang and Hsu (1974) reported 2n = 34 from a population of Taiwan, an amphidiploid (AABB), Karyotypes of other Chinese populations are worth further researches. 4. Tricyrtis macropoda Miq. The chromosome number of somatic cells is 2n= 26, and PMCs MII shows 13 bivalents (n= 13) (Plate 3:1-3, see Fig. 1:3 for its idiogram). The karyotype formula is 2n= 26= 6m + 10sm + 6st + 4st (or t), which is composed of chromosomes: 4L + 22S in size. The degree of asymmetry is of 3B. No centromeres of the 12th and 13th pairs of chromosomes were observed at metaphase, and the chromosomes may be of st or t. Nakamura (1968) reported 2n= 26(4L+ 22S)= 2sm+ 2sm-st+ 14st-sm+ 8st for T. macropoda Miq. and 2n= 26(4L+ 22S)= 8m+ 2sm+2sm-st+ 2st-sm+ 12st for its ssp. affinis, both from Japan. It is clear that the major character of their karyotypes, i. e. 4L + 22S, is consistent with that reported here. Based on the previous and present reports, all Tricyrtis species studied are remarkably uniform in the basic karyotype, i. e. 4L + 22S. 5. Allium macrostemon Bunge. The present observation on the root-tip cells of the species shows 2n = 32 (Plate 3: 4-5, see Fig. 1:4 for its idiogram). The karyotype formula is 2n (4x)= 32= 26m + 6sm, which belongs to 2B, being of high symmetry. Except the 6th, 10th and 13th pairs of chromosomes all the are metacentric. Chromosomes of this species are large, ranging from 5.94 to 18.06 μm. Our result agrees with Kawano’s (1975) report under the name of A. grayi Regel ( = A. macrostemon, Wang and Tang 1980). 6. Asparagus cochinchinensis (Lour.) Merr. Ten bivalents were observed in PMCs MI, n=10 (Plate 1: 1). The present result confirms the number of a population of Taiwan recorded by Hsu (1971). 7. Ophiopogon japonicus (L. f.) Ker-Gawl. The species from Mt. Taogui, Hangzhou, is found to have 2n (2x)=36=22m + 14sm (Plate 2: 1,5, see Fig. 1:5 for its idiogram) which belongs to 2B. The karyotype is composed of 2 medium-sized chromosomes with metacentric centromeres and 34 small chromosomes, ranging from 1.34 to 4.92 μm. The populations from Mt. Tianzhu and Mt. Yuling, Zhejiang, are found to be aneuploids at tetraploid level (2n=64-70). It is interesting that Nagamatsu (1971) found the karyotypes of Japanese materials to be 2n= 67 and 68, also showing unsteady 4x karyotypes of this species. In the previous. reports (see Table 1), the chromosome numbers of this species are mainly 2n = 72, besides 2n = 36 recorded by Sato (1942) from Japan. 8. Liriope platyphylla Wang et Tang The somatic complement of the species collected from Mt. Tianzhu, Hangzhou, is 2n = 36 (Plate 2: 3-4, see Fig. 1:6 for its idiogram). The karyotype is 2n(2x) = 36 = 16m + 20sm, belonging to 2B type. The chromosomes are small except the medium-sized, 1st pair and the range is from 1.27 to 5.19μm. The material from Mt. Yuling, Zhejiang, is found to have a variety of chromosome numbers (2n= 60-71), as observed in Ophiopogon japonicus. Hasegawa (1968) reported the karyotype of 2n = 72 (4x) from Japan The 2x karyotype is first recorded. This genus is closely related to Ophiopogon. Based on the Hasegawa’s and present studies, all the species in these two genera are remarkably uniform in karyo-type. Therefore, the taxonomy of the two genera is worth further researches.  相似文献   

5.
The present paper reports the chromosome numbers and karyotypes of eight species of Sect. Rhiziridium in Allium (Liaceae). The materials were all collected from their natural populations in east Inner Mongolia, China. The karyotype analysis is made on the basis of Li et al. (1985).The results are as follows (for chromosomes parameters, voucher specimens and localities, see Table 1 and Plate 1--2 the idiograms of the eight species in Fig. 1): (1) Auium leucocephalum Turcz. The somatic chromosome number and karyotype of this species is 2n=16=12m=2sm+2st (2SAT), in Stebbinsl(1971) kayotype classification, which belongs to 2A (Plate 1: 1; Fig. 1: 1). The range of chromosome relative length varies between 8.90--15.55%. Two small satellites are attached to the short arms of the 8th pair of chromosomes. (2) A. strictum Schrader has 2n (4x) =32=16m+4sm+12st, belonging to 2B (Plate 1: 2 & Fig. 1: 2). Satellites were not observed., and the range of chromosome relative length is between 3. 67-11.00%. (3) A. ramosum L. 2n=16=14m+ 2st (2SAT), belonging to 2A (Plate 1: 3 & Fig. 1: 3), Two small satellies are attached to the short arms of the 8th pair of chromosomes. The range of chromosome relative length is between 9.17-16.39%. The chromosome number and karyotype of this species are in accordancewith those reported by Li et al. (1982) with the material from Jinshan, Beijing. (4) A. bidentatum Fisch. ex Prokh. 2n (4x) =32=24m+4sm+4T, belonging to 2B (Plate 1: 4 & Fig. 1: 4). Satellites were not observed. A small median B-chromosome was found in root-tip cells of the population growing in sandy soil, and it is the first discovery (Plate 2: 9). The species has terminal chromosomes, which are seldom seen in Sect. Rhiziridium. The range of chromosome relative length is between 3.32—9.06%. (5) A. tenuissimu L. 2n=16= 10m+4sm+2st(2SAT), belonging to 2B(Plate 1:5 & Fig. 1:5). Two large satellites are attached to the short arms of the 8th pair of chromosome. The range of chromosome relative length is between 8.27--17.56%. (6)A. anisopodium Ledeb. 2n = 16 = l2m +2sm + 2st (2SAT), belonging to 2A (Plate 2:7 & Fig. 1: 7). Two large satellites are attached to the short arms of the 8th pair of chromosomes. In somatic cells of some plants of this species, a small submedian B-chromosome was found (Plate 2: 10, 11). The range of chromosome relative length is between 8.05-17.08 %. (7) A. anisopodium Ledeb. var. zimmermannianum (Gilg) Wang et Tang 2n (4x)=32=24m+4sm+4st( 4SAT), belonging to 2A (Plate 1: 6 & Fig. 1: 6). Four large satellites are attached to the short arms of the 15 and 16th pairs of chromosomes. The range of chromosome relative length is between 4.45--8.35%. This variety is similar to A. anisopodium Ledeb. in morphological characters, and their karyotype formulas are also very similar. The present authors consider that the variety is an allotetraploid derived from A. anisopodium Ledeb. (8) A. condensatum Turcz. 2n=16=14m+2st (2SAT), belonging to 2B (Plate 2:8 & Fig. 1:8). Two. small satellites are attached to the short arms of the 6th pair of chromosomes. In a few individuals of this species median (M) B-chromosome was discovered, and the number is stable (Plate 2: 12). The range of chromosome relative length is between 7.64--17.07%. In short, the chromosome numbers of the species studied in the present work are found to be 2n=16 or 32, and the karyotypes belong to 2A or 2B, highly symmetrical. The karyotypes of Chinese materials of these species are mostly reported for the first time. Threespecies have B-chromosomes.  相似文献   

6.
Lycoris radiata (L′Her. ) Herb. containing wild and cultural types, is distributed in China and Japan. The karyotype variation in three populations of the species from Anhui is studied in this paper. (1) Wuhu wild population has a karyotype 2n=21+1B= 1m+12st +8t+1B. The chromosomes range in length from 7.50 to 14.10 µm with the ratio of the longest to the shortest 1.88. The karyotype belongs to Stebbins’(1971) 3A. (2) Huangshan wild population has two cytotypes: 2n=22 and 2n=22+1B. Type Ⅰ: The karyotype formula is 2n=22=12st+10t. The chromosomes range in length from 6.85 to 9.95 µm. with the ratio of the longest to the shortest 1.45. The karyotype belongs to 4A. Type Ⅱ: The karyotype formula is 2n=22+1B=6st+14t+2T+1B (plate 1: 7,8). The chromosomes range in length from 6.50 to 11.02 µm. with the ratio of the longest to the shortest 1.70. The karyotype belongs to 4A. (3) Wuhu cultural type has a karyotype 2n=33=30st +3t. The chromosomes range in length from 7.10 to 9.35 µm with the ratio of the longest to the shortest 1.32. The karyotype belongs to 4A. This result agrees well with the previous reports. The diploid types of Lycoris radiata (L´Her.) Herb. are found in Anhui for the firsttime.  相似文献   

7.
The present paper deals with the karyotypic analysis of Taxodium ascendens Brongn. The somatic chromosomes in root-tip cells of the plant are found to be 2n =22, all with median and submedian constrictions. A character of the karyotype is that the chromosome 10 has a long kinetochore region (Plate 1:1). According to the terminology defined by Levan et al.[18], the karyotype formula is k(2n)=22=20m+2sm, which is different to Huang et Hsu’s[8] K(2n)=24=22m+2B(m). The karyotype belongs to “lA” of Stebbins’[24] karyotypic symmetry and is generally regarded as a relatively primitive one. The species’ chromosome complement is 2n=22=2L+8M2+12M1 according to I.R.L.difined by Kuo et al.[15] based on relative length. The lengths, arm ratios and types of chromosomes of the species are given in Table 1-I. The morphology of the chromosomes and the karyotype, are given in Plate 1:1. In the light of the works of Schlarbaum et al.[21] and Mehra et al.[17], K(2n)=22=20m (2SAT)+2sm and 2n=22=2L+6M2+14M1 are for T. distichum (L.) Rich. (see Table 1-II), K(2n)=20m+2sm and 2n=22=4L+4M2+12M1+2S for T. mucronatum Tenore (see Table 1-III, Plate 1:2), which belong to “lA” and “2A” respectively. The differences between three species in the ratio of the longest to the shortest chromosome, I.R.L. and the proportion of chromosomes with arm ratio >2 show that the karyotype of T. mucronatum is the most advanced and that of T. distichum the most primitive. The present author suggests that the sequence of evolutionary advance be T. distichum, T. ascendens, T. mucronatum. Based on the evidence from the karyotype analyses, ecology and geographical distribution (including fossil), the secondary center of genetic diversity (Fig. 1) and the probable evolu-tionary pattern (Fig. 2) of Taxodium are discussed.  相似文献   

8.
水松的细胞学研究   总被引:1,自引:0,他引:1  
李林初   《广西植物》1987,(2):101-106
本文报道了水松的核型公式K(2n)=22=22m,为“1A”类型。染色体相对长度组成为2n=22=2L+4M_2+16M_1。8号染色体具长着丝点区域,这是核型的一个特征。与近缘的国产种柳杉和水杉相比较。三者由原始到进化的顺序可能为(柳杉、水松)、水杉,水松与柳杉最接近,水杉和水松较近缘。本文还计算了水松的染色体体积。  相似文献   

9.
Lycoris sprengeri Comes ex Baker is endemic to China. Reported in the present paper are the chromosomes number and karyotypes for two wild populations of the species from Anhui. ( 1 )Caishi population has a karyotype 2n=33=9st+21t+3T. The length of chromosomes ranges from 5.58~9.15μm. The karyotype belongs to Stebbin’s (1971) “4A”. (2)Longyashan populations have two karyotypes. The karyotype formula of the type I is 2n=22=8st+14t, with chromosomes ranging from 6.88~9.15μm. The karyotype belongs to “4A”. The karyotype formula of the type Ⅱ is 2n=22=1m+1sm+14st+6t, with chromosomes ranging from 7.20~15.80μm. The karyotype belongs to “3B”. The triploid type of L. sprengeri was discovered in Anhui for the first time. The karyotype 2n=22 =1m+1sm+14st+6t in diploid type of this species is here reported for the first time.The Robertsonian change plays a key role in karyotype evolution of Lycoris.  相似文献   

10.
安徽黄精属的细胞分类学研究   总被引:10,自引:3,他引:7  
邵建章  张定成  钱枫   《广西植物》1994,14(4):361-368
本文首次报道黄精属PolygonatumMill我国三种特有植物的染色体数目和核型,结果如下:安徽黄精P.anhuiense发现两个细胞型:(1)2n=24=4m+6sm+14st;(2)2n=20=4m十6sm+10st;  黄精P.langyaensy2n=18=6m+8sm+4t;距药黄精P.franchetii有三个细胞型:(1)2n=22=8m+8sm(2sc)+6st;(2)2n=20=2m+14sm+4st;(3)2n=18=4m+8sm+4st+2T,全部属3B核型。黄精属植物安徽共有10种,本文对9种黄精的染色体数目、核型进行了比较研究,发现它们可划分成三个类群,与中国植物志(第十五卷)的形态分类基本相符。  相似文献   

11.
加拿大一枝黄花的核型分析及B染色体初报   总被引:7,自引:0,他引:7  
对安徽蚌埠地区外来植物加拿大一枝黄花的染色体核型进行了分析。结果如下:该入侵种的染色体数为2n=50,各染色体间形态差异不明显,均为中着丝粒或近中着丝粒染色体,最长与最短染色体相对长度比为1.72,全套染色体未见随体,核型公式为2 n=50=38 m 12 sm 6 B s,核型类型为较对称的2A型。首次报道了存在于体细胞中的异于常染色体的6个B染色体,这些B染色体在不同细胞中保持恒定的数目,并讨论了B染色体的存在与加拿大一枝黄花在新生境中具有入侵性之间的关系。  相似文献   

12.
二倍体石蒜在安徽发现   总被引:15,自引:2,他引:13  
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。  相似文献   

13.
车前属两种植物的核型研究   总被引:2,自引:0,他引:2  
张华宣   《广西植物》1998,18(2):119-122
本文对我国两种车前属Plantago植物的核型进行了分析。2个种的染色体数目均为2n=2x=12。它们的核型是:海滨车前P.camtschaticaLink,Enum.2n=2x=12=8m+4sm;毛车前P.jehohlensisKoidz.2n=2x=12=6m+4sm+2st。它们的核型均属“2A”型。由12条染色体组成。  相似文献   

14.
The chromosome numbers and karyotypes of 7 species of Smilax L. in Liliaceae (s. 1.) are cytotaxonomically studied in this work. Their karyotypic characters, distinction between the species and the chromosomal basis of sexual differentiation are discussed. The karyotypes of most species are first reported. The results are shown as follows (see Tables 1-4 for the chromosome parameters and the karyotype constitution; Fig. 1 for their idiograms): 1. Smilax nipponica Miq. The species is one of the herbaceous species distributed in East Asia. Two karyotypes, 2n = 26(type A) and 2n = 32 (type B), are found in the species (Plate 1: 1-7). The karyotype of No. 88032 (uncertain of -L--M--S- sexuality) is 2n = 26 = 2m + 6st + 6m + 4sm + 6sm + 2st. The karyotype has 4 pairs of L chromosomes, of which the first three pairs are subterminal, and the 4th is median. The karyotype belongs to 3B. No. 88045 (the male) and No. 88046 (the female) have 2n = 32. Their karyotypes are basically uniform, and both are -L--M-- S 2n=32= 2m+4sm+ 2st+ 2m+4sm+ 6m+ 10sm + 2st, also with 4 pairs of L chromosomes, but the 2nd pair is median, and thus different from the type A. The karyotype belongs to 3B. The first pair of chromosomes of the male are distinctly unequal in length, with the D. V. (0.93) of relative length between them obviously greater than that of the female (0.1). The pair seems to be of sex-chromosomes. Sixteen bivalents (n= 16) were observed at PMCs MI of No. 88045 (Plate 1: 4). The major difference between the karyotypes A and B are greater relative length of L chromosomes in the type A than in the type B, and the increase of chromosome number in the karyotype B mainly due to the increase of st chromosomes. Nakajima (1937)reports 2n= 30 for S. hederacea var. nipponica (=S. nipponica, Wang and Tang, 1980). 2. S. riparia A. DC. This species is also herbaceous, distributed in East Asia. Thirty chromosomes were found in root-tip cells (uncertain of sexuality). The kar -L--M--S-yotype is 2n = 30 = 8st + 6sm + 2st + 6m + 6sm + 2st (Plate 3: 1, 5), consisting mainly of sm and st chromosomes. There are 4 pairs of L chromosomes which are all subterminal and the m chromosomes appear to fall all into S category. Though the karyotype belongs to 3B, it is less symmetrical than that of S. nipponica. The species is karyologically rather different from S. nipponica, therefore. The first pair of chromosomes of this material are unequal in length, and it may be a male. The karyotype of this species is first reported. 3. S. sieboldii Miq. The species is a thorny climbing shrub, distributed in East Asia. At PMCs All, 16 chromosomes (n= 16) were found (Plate 2: 6), in accordance with Nakajima's (1933) report for a Japanese material. 4. S. china L. This species, a thorny climbing shrub, is of a wide distribution range mainly in East Asia and Southeast Asia. Two karyotypes were observed in different populations. (1) The population from Xikou has 2n = 96(6x) = 20st+L- -M- 6t + 6sm + 12st + 52(S) (Plate 3:7), of which the first three pairs of chromosomes are terminal, different from those in the other species. The arm ratios of both L and M chromosomes are larger than 2.0, which resembles those of S. davidiana. (2) PMCs MI of the population from Shangyu shew 15 chromosomes (n 15). The hexaploid of the species is recorded for the first time. Hsu (1967,1971) reported 2n = 30 from Taiwai and Nakajima (1937) recorded n = 30 from Japan, which indicates that the karyotype of the species varies not only in ploidy, but also in number. 5. S. davidiana A. DC. The somatic cells were found to have 32 chromosomes, and PMCs MI shew 16 bivalents (Plate 2: 1-5). The karyotype is 2n = 32=-L- -M- -S 8st + 4sm + 4st + 8sm + 8st. The karyotype belongs to 3B, and is less symmetrical than those in herbaceous species. The D. V. (0.20) of relative length between the two homologues of the first pair is slightly larger in the male than in the female (0.14), and it is thus difficult to determine whether they are sexual chromosomes or not. 6. S. glabra Roxb. The species is a non-thorny climbing shrub, distributed in East Asia and Southeast Asia. 32 chromosomes were found in somatic cells. The -L- -M- - Skaryotype is 2n= 32= 8st + 10st+6sm+8st (Plate 3: 2, 6),with only 3 pairs of sm chromosomes (12, 13 and 16th). The karyotype is more asymmetric than that of S. davidiana, although it is also of 3B (Table 1). The karyotype is first reported for the species. 7. S. nervo-marginata Hay. var. liukiuensis (Hay.) Wang et Tang The variety has a relatively narrow distribution range, mainly occurring in eastern China. The chromosomal number of somatic cells is 2n= 32 (Plate 3: 3-4). The karyotype is -L- -M- -S 2n = 32 = 2sm + 6st + 2sm + 2st + 2m + 6sm + 12st, evidently different from that of S. glabra. The first pair of chromosomes are submedian, and much longer than the 2nd to 4th pairs. The ratio in length of the largest chromosome to the smallest one is 4.3. The symmetric degree is of 3C, a unique type. The karyotype of the species is reported for the first time. In Smilax, the known basic numbers are 13, 15, 16 and 17. The two herbaceous species distributed in East Asia have three basic numbers: 13, 15 and 16, while the woody species studied mainly have 16, with no 13 recorded. Mangaly (1968) studied 8 herbaceous species in North America and reported 2n=26 for them except S. pseudo-china with 2n=30. Mangaly considered that a probably ancestral home of Smilax, both the herbaceous and woody, is in Southeast Asia and the eastern Himalayas, and speculated that the ancestral type of Sect. Coprosmanthus is possibly an Asian species, S. riparia. The karyotypes of the two herbaceous species in East Asia consist mostly of sm and m chromosomes, whereas those for the North American species are all of st chromosomes. Based on the general rule of karyotypic evolution, i.e. from symmetry to asymmetry, his speculation seems reasonable. Researches on sex-chromosomes of Smilax have been carried out since 1930 (Lindsay, 1930; Jensen, 1937; Nakajima, 1937; Mangaly, 1968), and they are generally considered to be the largest pair, but there is still no adequate evidence. The result of our observation on S. nipponica may confirm that the first pair of chromosomes of this species is XY type of sex-chromosomes. Chromosomes of the genus are small and medium-sized, varying between 1-6 μm, slightly larger in herbaceous species than in woody ones, larger in the karyotype of 2n=26 than in that of 2n=32. Based on karyotype constitution of the above 5 species, the karyotype in the genus is characterized by 4 pairs of L chromosomes and 2-5 pairs of M chromosomes, and mostly st and sm chromosomes, and by rather asymmetrical 3B type. The degree of symmetry in the above 5 species is from Sect. Coprosmanthus to Sect. Coilanthus, and herbaceous species towoody ones.  相似文献   

15.
Karyomorphological comparisons were made of six species of JapaneseLycopodium sensu stricto. There were no marked differences at interphase and prophase among the six species.Lycopodium annotinum had 2n=68 and the formula of its metaphase karyotype was 18m(median centromeric chromosomes)+12sm(submedian)+12st(subterminal)+26t(terminal).Lycopodium casuarinoides had 2n=68=16m+10sm+18st+24t,L. clavatum 2n=68=22m+12sm+18st+16t, andL. obscurum 2n=68=10m+22sm+20st+16t. Each of these species, which belong to different sections, displayed several karyomorphological differences. Among themL. casuarinoides differs largely from the others in its mean chromosome length, ratio of the longest chromosome to the shortest, and frequency of m+sm chromosomes. BothLycopodium complanatum andL. nikoense, belonging to sectionComplanata, had a common karyotype 2n=46=10m+12sm+18st+6t. This section displayed a low differentiation in its karyotype. In the wholeLycopodium s.s., the ratios of m+sm in a complement varied from 38 to 50%, being higher among pteridophytes.  相似文献   

16.
In the present paper the karyotypes of Smilacina tatsienensis (Franch.) Wang et Tang and Ophiopogon japonicus (L. f.) Ker.- Gawl. in Sichuan were analysed. The karyotypes of the two species are reported for the first time. The results are shown as follows. Smilacina tatsienensis (Franch.) Wang et Tang is a dipoiid. Its karyotype formula is 2n=2x=36=16m+10sm+10st(4SAT) (Plate 1: Fig. 1, 3). The karyotype is bimodal with ten large and eight small chromosome pairs and the length ratio of the tenth pair to the eleventh being 1.33. The length ratio of the largest chromosome and the smallest one is 4.33. Ophiopogon japonicus (L.f.) Ker.-Gawl. is a mixoploid, with diploid, triploid and tetraploid cells in a single plant. The karyotype formula of the diploid is 2n=2x=36=18m (4SAT)+18sm(Plate 1: Fig. 2, 4). The species is of a bimodal karyotype with eight large and ten small chromosome pairs and the length ratio to the eighth pair and the ninth being 1.10.There are nine metacentric pairs (two pairs of sat-chromosomes) and nine submetacentric pairs.  相似文献   

17.
本文对国产6种黄精的染色体数目和核型进行了研究,结果为:康定玉竹2n=28=6m+8sm+14st;狭叶黄精2n=30=12m+12sm+6st;毛筒玉竹2n=22=6m+6sm+10st;大苞黄精2n=22=4m+12sm+6st;轮叶黄精有两种细胞型,分别为2n=54和2n=58;点花黄精2n=90;此外,在部分类群中还发现有明显的杂合现象。作者通过与现有资料进行对比,对各类群染色体数目和结构变异的特点和机制进行了初步分析。  相似文献   

18.
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.  相似文献   

19.
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.  相似文献   

20.
Karyotype analysis for the species Reineckia carnea (Andr.) Kunth of the monotypic genus Reineckia Kunth is given for the first time. The number of chromosomes in root-tip cell was found to be 38, which is in accord with those reported by most of the previous authors[5,7,8,9,11,12,]. The somatic complement shows a slight variation in size, i.e., the 2, 3, 5, 6, 7th pairs of the chromosomes have submedian constrictions, while the other pairs have median centromeres. The karyotype is therefore a rather symmetrical one, and according to the chromosomal terminology defined by Levan et al[4], the karyotype formula of the species is 2n=38=28 m+10 sm. In spite of the presence of two nucleoli in the telophase as observed by the authors and Noguchi[8] as well, the two corresponding Sat-chromosomes have not been found. Photomicrograph of the chromosome complement and idiogram are given in Fig. 1 and 2 respectively.  相似文献   

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