scholarly journals Relations and evolution in Cheilanthes (Sinopteridaceae, Pteridophita) in Macaronesia and Mediterranean area, deduced from genome analysis of their hybrids

1983 ◽  
Vol 8 ◽  
pp. 101-126 ◽  
Author(s):  
G. Vida ◽  
A. Major ◽  
T. Reichstein
Keyword(s):  
Chromosome Number ◽  
Genome Analysis ◽  
Chromosome Doubling ◽  
Diploid Species ◽  
Mediterranean Area ◽  
Basic Chromosome Number ◽  
The Other ◽  
Experimental Conditions ◽  
Natural Group ◽  
Basic Chromosome

Nine species of "Cheilantoid ferns" are known to grow in Macaronesia and the Mediterranean basin. Two of them (lacking a pseudo-indusium and having the basic chromosome number X = 29), both aggregate species which we prefer to retain in Notholaena, are not included in this study. The other seven species (with distinct pseudo-indusium and the basic chromosome number X = 30), which we accept as members of the genus Cheilanthes Sw. sensu stricto, were subjected to detailed genome analysis of their natural and experimentally produced hybrids and shown to represent an aggregate of four very distinct ancestral diploids and three allotetraploids. The latter must have once been formed by chromosome doubling in the three diploid hybrids of C. maderensis Lowe with the other three diploid species. Theoretically three more allotetraploids would be possible but their formation has obviously been prevented by the geographical separation of the three respective diploids. The most widely distributed of the tetraploids, i.e. C. pteridioides (Reich.) C.Chr. has also been resynthesized from its ancestors (still sympatric) under experimental conditions. The intermediate morphology of the allotetraploids (as compared with their diploid ancestors) is obviously the reason why their status and existence has so long escaped recognition in Europe. These seven species form a natural group and, in our opinion, should not be divided into sections.

The biosystematics of the genus Lotus (Leguminosae) in Canada. II. Numerical chemotaxonomy

1968 ◽  
Vol 46 (5) ◽  
pp. 585-589 ◽  
Author(s):  
William F. Grant ◽  
Ilse I. Zandstra
Keyword(s):  
Chromosome Number ◽  
Thin Layer ◽  
Native Species ◽  
Cytological Study ◽  
Diploid Species ◽  
Basic Chromosome Number ◽  
Chromatographic Study ◽  
Chemical Identification ◽  
Basic Chromosome ◽  
Fluorescent Compounds

A thin-layer chromatographic study of fluorescent compounds present in native (L. denticulatus, L. formosissimus, L. micranthus, L. pinnatus, L. purshianus) and introduced (L. corniculatus, L. krylovii, L.pedunculatus, L. tenuis) Canadian species of Lotus has been carried out and relationships of the species have been determined on the basis of the coefficients of association of these compounds. Chemical identification of the compounds was not attempted, but test reagents indicated a number to be phenolics. The analysis supported the general taxonomic relationships of the species based on a morphological and cytological study. Of the native species, L. pinnatus and L. formosissimus were the most closely related, with a coefficient of association of 83.33. Lotus denticulatus, the only native species with a chromosome number of n = 6, in general showed lower coefficients of association with the n = 7 species. Of the introduced species, all of which belong to the L. corniculatus group with a basic chromosome number of 6, L. krylovii and L. tenuis had the highest coefficient of association, 75.86. Based on their coefficients of association, both of these diploid species were more closely related to the tetraploid L. corniculatus than to the diploid L. pedunculatus.

Phylogenetics and chromosomal evolution in the Poaceae (grasses)

2004 ◽  
Vol 52 (1) ◽  
pp. 13 ◽  
Author(s):  
Khidir W. Hilu
Keyword(s):  
Chromosome Number ◽  
Chromosome Numbers ◽  
Chromosome Doubling ◽  
Chromosomal Evolution ◽  
Basic Chromosome Number ◽  
Basic Chromosome ◽  
Wide Range ◽  
The Family

The wide range in basic chromosome number (x = 2–18) and prevalence of polyploidy and hybridisation have resulted in contrasting views on chromosomal evolution in Poaceae. This study uses information on grass chromosome number and a consensus phylogeny to determine patterns of chromosomal evolution in the family. A chromosomal parsimony hypothesis is proposed that underscores (1) the evolution of the Joinvilleaceae/Ecdeiocoleaceae/Poaceae lineage from Restionaceae ancestors with x = 9, (2) aneuploid origin of x�=�11 in Ecdeiocoleaceae and Poaceae (Streptochaeta, Anomochlooideae), (3) reduction to x = 9, followed by chromosome doubling within Anomochlooideae to generate the x = 18 in Anomochloa, and (4) aneuploid increase from the ancestral x = 11 to x = 12 in Pharoideae and Puelioideae, and further diversification in remaining taxa (Fig. 3b). Higher basic chromosome numbers are maintained in basal taxa of all grass subfamilies, whereas smaller numbers are found in terminal species. This finding refutes the 'secondary polyploidy hypothesis', but partially supports the 'reduction hypothesis' previously proposed for chromosomal evolution in the Poaceae.

Infrageneric phenetic relations in new world Panicum (Poaceae: Panicoideae: Paniceae): a numerical analysis

1993 ◽  
Vol 71 (10) ◽  
pp. 1312-1327 ◽  
Author(s):  
Fernando Zuloaga ◽  
Jorge Dubcovsky ◽  
Osvaldo Morrone
Keyword(s):  
Chromosome Number ◽  
Basic Chromosome Number ◽  
The Other ◽  
Mestome Sheath ◽  
Basic Chromosome ◽  
Group 4 ◽  
Group 3 ◽  
Group 5 ◽  
Group 2 ◽  
Phenetic Relations

Numerical studies based on 64 characters placed 188 American species of the genus Panicum L. in 23 sections clustered in five major groups. The same major groups were obtained when the five characters that define the subgenera were excluded from the analyses. Groups 1 and 2 included C4 species. Species with an outer parenchymatous sheath in group 1 corresponded to subg. Panicum, whereas species with a single mestome sheath in group 2 corresponded to subg. Agrostoides. Group 3 included the intermediate C3–C4 species belonging to subg. Steinchisma. C3 sections were clustered together but arranged in a different way than previous classifications. Group 4 included sections from subg. Phanopyrum with basic chromosome number x = 10, whereas group 5 included the other sections of Phanopyrum with x = 9 together with sections from subg. Dichanthelium also with x = 9. The two subgroups of subg. Phanopyrum are not only different in chromosome number but also in inflorescence type and upper anthecium ornamentation. On the other hand the x = 9 sections of Phanopyrum remain in the same cluster with sections from subg. Dichanthelium in numerical analyses where basic chromosome number is removed. These results suggest the possibility of sinking Dichanthelium into Phanopyrum and then split the latter when more cytological data become available. Kranz syndrome and basic chromosome number were the characters with the highest contribution to the delimitation of the major groups. On the basis of these results different existing hypotheses on the classification of the genus Panicum are discussed. Key words: Panicum, numerical taxonomy.

Cytotaxonomy of Allium (Amaryllidaceae) subgenera Cyathophora and Amerallium sect. Bromatorrhiza

Phytotaxa ◽  
2017 ◽  
Vol 331 (2) ◽  
pp. 185 ◽  
Author(s):  
MIN-JIE LI ◽  
XIAN-LIN GUO ◽  
JUAN LI ◽  
SONG-DONG ZHOU ◽  
QING LIU ◽  
...  
Keyword(s):  
Chromosome Number ◽  
Chromosome Numbers ◽  
Karyotype Evolution ◽  
Diploid Species ◽  
Basic Chromosome Number ◽  
Molecular Evidence ◽  
Basic Chromosome ◽  
Karyotype Asymmetry

In the present study, we examined the karyotype data of subg. Cyathophora and sect. Bromatorrhiza, to determine some disputed karyotypes (e.g., A. spicatum and A. fasciculatum), and further to estimate the karyotype evolution along their phylogenetic frameworks. Our results revealed a fairly stable basic chromosome number (x = 8) in subg. Cyathophora, and we therefore revised x = 8 as the basic chromosome number of A. spicatum, rather than x = 10 mostly due to misidentifications concerning A. fasciculatum. The karyotype asymmetry analyses for subg. Cyathophora indicated that, the karyotype evolution for diploid species showing a high karyotype similarity was mainly due to intrachromosomal changes, while the interchromosomal changes were linked to the evolution of tetraploid populations. However, indeed different dysploid basic chromosome numbers (x = 7, 10, 11) and greatly different karyotype patterns occurred in sect. Bromatorrhiza, corresponding to the subsections revealed by molecular evidence. The combined evidence suggested that species with x = 11 compose a segmental allotriploid complex. It was also indicated that karyotype pattern of polyploids usually is closely related with  their diploid progenitors.

scholarly journals Variation in Ribosomal DNA in the Genus Trifolium (Fabaceae)

Plants ◽  
2021 ◽  
Vol 10 (9) ◽  
pp. 1771
Author(s):  
Radka Vozárová ◽  
Eliška Macková ◽  
David Vlk ◽  
Jana Řepková
Keyword(s):  
Chromosome Number ◽  
Ribosomal Dna ◽  
Chromosome Numbers ◽  
Evolutionary History ◽  
Diploid Species ◽  
Basic Chromosome Number ◽  
Rdna Site ◽  
Ancestral State ◽  
Basic Chromosome ◽  
26S Rdna

The genus Trifolium L. is characterized by basic chromosome numbers 8, 7, 6, and 5. We conducted a genus-wide study of ribosomal DNA (rDNA) structure variability in diploids and polyploids to gain insight into evolutionary history. We used fluorescent in situ hybridization to newly investigate rDNA variation by number and position in 30 Trifolium species. Evolutionary history among species was examined using 85 available sequences of internal transcribed spacer 1 (ITS1) of 35S rDNA. In diploid species with ancestral basic chromosome number (x = 8), one pair of 5S and 26S rDNA in separate or adjacent positions on a pair of chromosomes was prevalent. Genomes of species with reduced basic chromosome numbers were characterized by increased number of signals determined on one pair of chromosomes or all chromosomes. Increased number of signals was observed also in diploids Trifolium alpestre and Trifolium microcephalum and in polyploids. Sequence alignment revealed ITS1 sequences with mostly single nucleotide polymorphisms, and ITS1 diversity was greater in diploids with reduced basic chromosome numbers compared to diploids with ancestral basic chromosome number (x = 8) and polyploids. Our results suggest the presence of one 5S rDNA site and one 26S rDNA site as an ancestral state.

scholarly journals Taxonomic Relationships of A Rare Cucumis Species (C. hystrix Chakr.) and Its Interspecific Hybrid with Cucumber

HortScience ◽  
2006 ◽  
Vol 41 (3) ◽  
pp. 571-574 ◽  
Author(s):  
Fei-Yun Zhuang ◽  
Jin-Feng Chen ◽  
Jack E. Staub ◽  
Chun-Tao Qian
Keyword(s):  
Chromosome Number ◽  
Interspecific Hybrid ◽  
Dna Analysis ◽  
Chromosome Doubling ◽  
Effective Means ◽  
Geographic Location ◽  
Basic Chromosome Number ◽  
Arbitrary Primers ◽  
Basic Chromosome ◽  
Taxonomic System

The current Cucumis taxonomic classification places C. hystrix Chakr. in subgen. Cucumis based on its morphological similarities to cucumber (C. sativus L., 2n = 14). However, the chromosome number of C. hystrix was identified as 2n = 24, the same number as in subgen. Melo. Cucumis hystrix is therefore considered the first wild Cucumis species of Asiatic origin possessing 12 basic chromosomes. Thus, any research regarding its biosystematics would challenge the basic chromosome number and geographic location theories that govern the current taxonomic system. The production of the amphidiploid species (Cucumis ×hytivus Chen and Kirkbride, 2n = 38) obtained from the cross between C. hystrix and C. sativus and subsequent chromosome doubling would provide an effective means of investigating the relationship between Cucumis species with two different basic chromosome numbers. Thus, RAPD markers were used to study the taxonomic placement of C. hystrix and its interspecific hybrid with cucumber. Of the 220 arbitrary primers screened, 31 were used for analysis where 402 (96.3%) fragments were polymorphic among the germplasm examined. A UPGMA-based cluster analysis partitioned 31 accessions into two main groups [C. sativus (CS) and C. melo (CM)]. Under the similarity coefficient threshold of 0.23, these two groups can be further divided into five clusters with C. hystrix, C. ×hytivus, and C. sativus as separate clusters in the CS group. A modified taxonomic system is proposed based on these results and findings of a previous chloroplast DNA analysis with the genus Cucumis containing subgen. Cucumis with three species and subgen. Melo with six series.

scholarly journals Karyotype and genome size variation in white-flowered Eranthis sect. Shibateranthis (Ranunculaceae)

PhytoKeys ◽  
2021 ◽  
Vol 187 ◽  
pp. 207-227
Author(s):  
Elizaveta Yu. Mitrenina ◽  
Andrey S. Erst ◽  
Lorenzo Peruzzi ◽  
Mikhail V. Skaptsov ◽  
Hiroshi Ikeda ◽  
...  
Keyword(s):  
Chromosome Number ◽  
Diploid Species ◽  
Size Variation ◽  
Chromosome Length ◽  
Basic Chromosome Number ◽  
Somatic Chromosome Number ◽  
Genome Size Variation ◽  
Basic Chromosome ◽  
Acrocentric Chromosomes ◽  
Intrachromosomal Asymmetry

Comparative karyomorphological analyses of six out of the eight white-flowered species of Eranthis sect. Shibateranthis have been carried out. All studied specimens of E. byunsanensis, E. lobulata, E. pinnatifida, and E. stellata had a somatic chromosome number 2n = 16 with basic chromosome number x = 8. On the contrary, E. tanhoensis and E. sibirica had a basic chromosome number x = 7. The specimens of E. tanhoensis were diploid with 2n = 14, while the specimens of E. sibirica were polyploid with 2n = 42. Monoploid chromosome sets of the investigated diploid species had 4–5 metacentric chromosomes and 2–4 submetacentric/subtelocentric/acrocentric chromosomes. The highest level of interchromosomal asymmetry, estimated via CVCL, was found in E. byunsanensis and E. pinnatifida. The highest levels of intrachromosomal asymmetry (MCA) and heterogeneity in centromere position (CVCI) were found in E. lobulata and E. byunsanensis, while E. sibirica had the most symmetric karyotype. A multivariate PCoA analysis of basic karyotype parameters (2n, x, THL, CVCL, MCA, and CVCI) highlighted no overlap among species accessions, which was also confirmed by LDA. The average absolute monoploid DNA content (1Cx) of the 23 investigated samples of six Eranthis species varied from 9.26 ± 0.25 pg in E. sibirica to 15.93 ± 0.32 pg in E. stellata. Overall karyological affinity was highlighted between E. lobulata and E. stellata, on one side, and between E. byunsanensis and E. pinnatifida, on the other side. Interestingly, there was no significant correlation between total haploid (monoploid) chromosome length (THL) and 1Cx values in these species.

scholarly journals In vitro propagation and cytological analysis of Sophora mollis Royle: an endangered medicinal shrub

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Aakriti Bhandari ◽  
Harminder Singh ◽  
Amber Srivastava ◽  
Puneet Kumar ◽  
G. S. Panwar ◽  
...  
Keyword(s):  
Chromosome Number ◽  
Average Length ◽  
Germplasm Conservation ◽  
Basic Chromosome Number ◽  
Shoot Tip ◽  
Ex Situ ◽  
Ms Medium ◽  
Basic Chromosome ◽  
Shoot Tip Explants

Abstract Background Sophora mollis Royle (family Fabaceae, subfamily-Papilionaceae) is a multipurpose legume distributed in plains and foothills of the North-West Himalaya to Nepal and is facing high risk of extinction due to habitat loss and exploitation by the local people for its fuel and fodder values. Therefore, the present study was conducted to standardize a micropropagation protocol for Sophora mollis by using shoot tip explants and to study the meiotic chromosome count in the species. Results Multiple shoots were induced in shoot tip explants of Sophora mollis in Murashige and Skoog medium supplemented with different concentrations of cytokinins alone (BAP, TDZ, and Kinetin) and in combination with varying concentrations of NAA. MS medium supplemented with BAP (8.9 μM) was observed to be the optimal medium for multiple shoot induction and maximum 25.32 shoots per explant was obtained with average length of 4.5 ± 0.8 cm. In vitro developed shoots were transferred onto rooting media supplemented with different concentrations of auxin (IAA, IBA, and NAA). Maximum 86% rooting was observed in half-strength MS medium supplemented with 21.20 μM NAA with an average of 21.26 roots per culture. In vitro raised plantlets were adapted to greenhouse for better acclimatization and 60% plants were successfully transferred to the open environment. Based on the chromosome counts available from the literature and the current study, the species tend to show a basic chromosome number of x = 9. Conclusion The micropropagation protocol standardized can be helpful for the ex situ mass multiplication and germplasm conservation of the endangered species. Moreover, the ex situ conservation approach will be helpful in actively bridging the gap between ex situ and in situ approaches through the reintroduction of species in the wild. The cytological studies revealed the basic chromosome number x = 9 of the species.

Meiotic chromosome behaviour in Cenchrus ciliaris

Bothalia ◽  
1998 ◽  
Vol 28 (1) ◽  
pp. 83-90 ◽  
Author(s):  
N. C. Visser ◽  
J. J. Spies
Keyword(s):  
Chromosome Number ◽  
Meiotic Chromosome ◽  
Basic Chromosome Number ◽  
Chromosome Behaviour ◽  
Meiotic Abnormalities ◽  
Single Specimen ◽  
Cenchrus Ciliaris ◽  
Basic Chromosome ◽  
Single Genome ◽  
Meiotic Irregularities

A basic chromosome number of x = 9 has been confirmed for Cenchrus ciliaris L. Polyploidy is common and levels vary from tetraploid to hexaploid. Aneuploidv is reported for a single specimen, where two chromosomes of a single genome were lost. Various meiotic irregularities were observed. The highest incidence of meiotic abnormalities was observed in the pentaploid specimens. This was attributed to their uneven polyploid level All specimens varied from segmental alloploid to alloploid.

Chromosome studies on African plants. 9. Chromosome numbers in Ehrharta (Poaceae: Ehrharteae)

Bothalia ◽  
1989 ◽  
Vol 19 (1) ◽  
pp. 125-132 ◽  
Author(s):  
J. J. Spies ◽  
E. J. L. Saayman ◽  
S. P. Voges ◽  
G. Davidse
Keyword(s):  
Chromosome Number ◽  
Ploidy Level ◽  
Chromosome Numbers ◽  
Basic Chromosome Number ◽  
B Chromosomes ◽  
Basic Chromosome ◽  
Cytogenetic Studies ◽  
African Plants ◽  
First Time

Cytogenetic studies of 53 specimens of 14 species of the genus  Ehrharta Thunb. confirmed a basic chromosome number of 12 for the genus. Chromosome numbers for 13 species are described for the first time. The highest ploidy level yet observed in the genus (2n = lOx = 120) is reported for E. villosa var.  villosa. B chromosomes were observed in several specimens of four different species.

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