Cytology, fertility, and morphology of Elymus kengii (Keng) Tzvelev and E. grandiglumis (Keng) A. Löve (Triticeae: Poaceae)

Genome ◽  
1990 ◽  
Vol 33 (4) ◽  
pp. 563-570 ◽  
Author(s):  
Kevin B. Jensen

This study reports on the cytogenetics, fertility, mode of reproduction, and morphological variation of two perennial Triticeae grasses, Elymus kengii (Keng) Tzvelev and Elymus grandiglumis (Keng) A. Löve, from west central China. Both species are allohexaploids (2n = 42), self-fertile, and morphologically distinct on the basis of their plant color, glume length, and lemma and rachis vestiture. F1 hybrids between these two species are partially fertile and morphologically intermediate to their parents. Analysis of chromosome pairing in hybrids between E. grandiglumis or E. kengii and the following "analyzer" species, Psathyrostachys juncea (Fisch.) Nevski (NN), Psathyrostachys huashanica Keng (NN), Elymus lanceolatus (Scribn. &Smith) Gould (SSHH), Elymus dentatus (Hook. f.) Tzvelev ssp. ugamicus (Drob.) Tzvelev (SSYY), Elymus ciliaris (Trin.) Nevski (SSYY), Pseudoroegneria spicata (Pursh) A Löve (SS), and Pseudoroegneria tauri (Boiss. &Bal.) A. Löve (SSPP), suggested that both taxa contain the S, Y, and P genomes. This represents a new genome combination not previously reported and shows that the P genome from the crested wheatgrasses (Agropyron) has been involved in polyploid evolution within the. Triticeae.Key words: genome, meiosis, chromosome pairing, interspecific hybrids, Elymus, Triticeae.

Genome ◽  
1991 ◽  
Vol 34 (6) ◽  
pp. 860-867 ◽  
Author(s):  
Kevin B. Jensen ◽  
Richard R.-C. Wang

Two accessions of Elymus caucasicus (Koch) Tzvelev and three accessions of Elymus longearistatus (Boiss.) Tzvelev were studied to determine the meiotic behavior and chromosome pairing in the two taxa, their interspecific hybrid, and their hybrids with various "analyzer" parents. Interspecific and intergeneric hybrids of the target taxa were obtained with the following analyzer species: Pseudoroegneria spicata (Pursh) A. Löve (2n = 14, SS), Pseudoroegneria libanotica (Hackel) D. R. Dewey (2n = 14, SS), Hordeum violaceum Boiss. &Hohenacker (2n = 14, HH) (= Critesion violaceum (Boiss. &Hohenacker) A. Löve), Elymus lanceolatus (Scribn. &Smith) Gould (2n = 28, SSHH), Elymus abolinii (Drob.) Tzvelev (2n = 28, SSYY), Elymus pendulinus (Nevski) Tzvelev (2n = 28, SSYY), Elymus fedtschenkoi Tzvelev (2n = 28, SSYY), Elymus panormitanus (Parl.) Tzvelev (2n = 28, SSYY), and Elymus drobovii (Nevski) Tzvelev (2n = 42, SSHHYY). Cytological analysis of their F1 hybrids showed that E. caucasicus and E. longearistatus were allotetraploids comprising the same basic genomes. Chromosome pairing in the E. caucasicus × P. libanotica hybrid demonstrated that the target taxa contained the S genome, based on 6.1 bivalents per cell. The lack of chromosome pairing, less than one bivalent per cell, in the E. longearistatus × H. violaceum hybrid showed that the H genome was absent. Increased pairing in the tetraploid and pentaploid hybrids when the Y genome was introduced indicated that the second genome in the two taxa was a segmental homolog of the Y genome. The S and Y genomes in E. caucasicus and E. longearistatus have diverged from each other and from those in many of the eastern and central Asian SY tetraploids.Key words: genome, meiosis, chromosome pairing, morphology, hybrid, Triticeae.


Genome ◽  
1993 ◽  
Vol 36 (1) ◽  
pp. 147-151 ◽  
Author(s):  
J. Torabinejad ◽  
R. J. Mueller

Eight intergeneric hybrid plants were obtained between Elymus scabrus (2n = 6x = 42, SSYY??) and Australopyrum pectinatum ssp. retrofractum (2n = 2x = 14, WW). The hybrids were vegetatively vigorous but reproductively sterile. Examination of pollen mother cells at metaphase I revealed an average of 16.63 I, 5.29 II, 0.19 III, and 0.05 IV per cell for the eight hybrids. The average chiasma frequency of 6.77 per cell in the above hybrids strongly supports the presence of a W genome from A. pectinatum ssp. retrofractum in E. scabrus. Meiotic pairing data of some other interspecific hybrids suggest the existence of the SY genomes in E. scabrus. Therefore, the genome constitution of E. scabrus should be written as SSYYWW. Two other hybrid plants resulted from Elymus yezoensis (2n = 4x = 28, SSYY) crosses with A. pectinatum ssp. pectinatum (2n = 2x = 14, WW). Both were weak and sterile. An average of 0.45 bivalents per cell were observed at metaphase I. This clearly indicates a lack of pairing between W genome of Australopyrum and S or Y genomes of E. yezoensis. In addition, six hybrid plants of E. scabrus with Psathyrostachys juncea (2n = 2x = 14, NN) and one with Thinopyrum bessarabicum (2n = 2x = 14, JJ) were also obtained. The average bivalents per cell formed in both combinations were 2.84 and 0.70, respectively. The results of the latter two combinations showed that there is no N or J genome in E. scabrus.Key words: wide hybridization, chromosome pairing, genome analysis, Australopyrum, Elymus.


1986 ◽  
Vol 28 (5) ◽  
pp. 770-776 ◽  
Author(s):  
Kevin B. Jensen ◽  
Douglas R. Dewey ◽  
Kay H. Asay

Elymus alatavicus (Drob.) A. Love and E. batalinii (Krasn.) A. Love were studied to determine (i) meiotic behaviour, (ii) the mode of reproduction, (iii) the relationship between the two species, (iv) genomic constitutions, and (v) the most logical taxonomic classification of both species. A series of F1 hybrids between E. alatavicus, E. batalinii, and six "analyzer" species were developed. Chromosome pairing was studied at metaphase I to identify genomic similarities or differences. The results showed that E. alatavicus and E. batalinii are caespitose, self-fertile allohexaploids (2n = 42) with the same genomic formula SSYYXX. The F1 hybrids between E. alatavicus and E. batalinii had complete pairing (21 bivalents) at metaphase I in 7% of the cells and almost complete pairing in the remaining cells. High chromosome pairing and partial fertility (4 seeds/plant) in the F1 hybrids shows that the two species are closely related. Hybrids were obtained between E. alatavicus or E. batalinii and the following "analyzer" species with known genomic formulas: Pseudoroegneria spicata (Pursh) A. Love, 2n = 14, SS; P. cognata (Hack.) A. Love, 2n = 14, SS; E. lanceolatus (Scribn. &Smith) Gould, 2n = 28, SSHH; E. trachycaulus1 (Link) Gould ex Shinners, 2n = 28, SSHH; E. mutabilis (Drob.) Tzvelev, 2n = 28, SSHH; and E. drobovii (Nevski) Tzvelev, 2n = 42, SSHHYY. Chromosome pairing in this series of hybrids demonstrated that E. alatavicus and E. batalinii contain an S and probably a Y genome plus an unknown genome, X, that may have been derived from Psathryostachys huashanica Keng or from Agropyron. Elymus alatavicus and E. batalinii are correctly classified in the genus Elymus.Key words: cytotaxonomy, Agropyron, meiosis, chromosome.


Crop Science ◽  
1991 ◽  
Vol 31 (5) ◽  
pp. 1391-1391 ◽  
Author(s):  
K. H. Asay ◽  
D. R. Dewey ◽  
K. B. Jensen ◽  
W. H. Horton ◽  
K. W. Maughan ◽  
...  

1970 ◽  
Vol 12 (4) ◽  
pp. 790-794 ◽  
Author(s):  
Chi-Chang Chen ◽  
Pryce B. Gibson

Both Trifolium repens (2n = 32) and T. nigrescens (2n = 16) formed bivalents during meiosis. However, their triploid hybrid showed an average of 4.27 trivalents per microsporocyte at metaphase I. The frequency of trivalents in the hybrid between T. nigrescens and autotetraploid T. occidentale (2n = 32) was 5.69. The data are interpreted to indicate: (1) a possible autotetraploid origin of T. repens; and (2) a close phylogenetic relationship among T. repens, T. nigrescens and T. occidentale.


1983 ◽  
Vol 25 (5) ◽  
pp. 530-539 ◽  
Author(s):  
Jan Dvořák

Data on chromosome pairing in haploids and interspecific hybrids of Solanum, sect. Petota reported in the literature were used to determine whether the diploidlike chromosome pairing that occurs in some of the polyploid species of the section is regulated by the genotype or brought about by some other mechanism. The following trends emerged from these data. Most of the polyploid × polyploid hybrids had high numbers of univalents, which seemed to indicate that the polyploid species were constructed from diverse genomes. Haploids, except for those derived from S. tuberosum, had incomplete chromosome pairing. All hybrids from diploid × diploid crosses had more or less regular chromosome pairing, which suggested that all investigated diploid species have the same genome. Likewise, hybrids from polyploid × diploid crosses had high levels of chromosome pairing. These paradoxical results are best explained if it is assumed that (i) the genotypes of most polyploid species, but not those of the diploid species, suppress heterogenetic pairing, (ii) that nonstructural chromosome differentiation is present among the genomes of both diploid and polyploid species, and (iii) the presence of the genome of a diploid species in a polyploid × diploid hybrid results in promotion of heterogenetic pairing. It is, therefore, concluded that heterogenetic pairing in most of the polyploid species is genetically suppressed.


1997 ◽  
Vol 75 (12) ◽  
pp. 2146-2157 ◽  
Author(s):  
Elisabeth Huber-Sannwald ◽  
Martyn M. Caldwell ◽  
David A. Pyke

A previous study showed that clonal morphology of the rhizomatous grass Elymus lanceolatus ssp. lanceolatus (Scibner & J.G. Smith Gould) was influenced more by neighbouring root systems than by the local distribution of nutrients. In this study we determine whether individual rhizomes or roots of E. lanceolatus perceive neighbouring root systems and how this is manifested in morphological responses of E. lanceolatus clones. Elymus lanceolatus was grown in the same bin with Pseudoroegneria spicata (Pursh) A. Love or Agropyron desertorum (Fisch. ex Link) Schult. plants. Elymus lanceolatus was separated from its neighbours by different barriers. The barriers allowed either only E. lanceolatus roots; only a single E. lanceolatus primary rhizome; or both roots and rhizomes to contact the neighbour root system. When only a single E. lanceolatus primary rhizome with potentially developing branching rhizomes made contact with the neighbour, the clonal structure of E. lanceolatus was modified more with P. spicata as the neighbour than with A. desertorum. With root contact of E. lanceolatus alone there was a similar effect with the neighbouring plants, but there was a more marked inhibitory effect on E. lanceolatus clonal growth with P. spicata than with A. desertorum, compared with the treatment with only a single rhizome in contact with the neighbour. Root resource competition in the unconstrained treatment (roots and rhizomes) between neighbouring plant and E. lanceolatus was more apparent with A. desertorum than with P. spicata. This study is one of the first to document that rhizome and root contact of a clonal plant with its neighbours may induce different clonal responses depending on the species of neighbour. Key words: Agropyron desertorum, clonal morphology, Elymus lanceolatus ssp. lanceolatus, plant interference, plant contact, Pseudoroegneria spicata, rhizome structure, root systems.


Genome ◽  
1989 ◽  
Vol 32 (4) ◽  
pp. 640-645 ◽  
Author(s):  
K. B. Jensen ◽  
C. Hsiao ◽  
K. H. Asay

Agropyron vaillantianum (Wulf. &Schreber) Trautv. and E. arizonicus (Scribn. &Smith) Gould were studied to describe their (i) reproductive characteristics, (ii) meiotic behavior, (iii) genomic constitution, and (iv) correct taxonomic alignment based on genomic relationships. Both species were found to be self-fertile tetraploids (2n = 28) and behaved as strict allotetraploids averaging 14.00 and 13.77 bivalents per cell, respectively. The hybrids A. vaillantianum × Pseudoroegneria spicata (Pursh) A. Love, 2n = 14, SS, A. vaillantianum × E. trachycaulus (Link) Gould ex Shinners, 2n = 28, SSHH, and E. arizonicus × E. canadensis L., 2n = 28, SSHH, averaged 6.21, 12.56, and 12.60 bivalents per cell, respectively. Chromosome pairing in this series of hybrids demonstrated that A. vaillantianum and E. arizonicus contain the S and H genomes, with each taxon having a slight modification resulting from evolutionary pressures under different ecological parameters. On the basis of chromosome pairing and mode of pollination it is proposed that A. vaillantianum be treated in the genus Elymus rather than in the genus Agropyron, with the following new name combination: Elymus vaillantianus (Wulf. &Schreb.) K. B. Jensen comb.nov., based on Triticum vaillantianum Wulfen &Schreber. Elymus typically encompasses those species that are self-fertile, and contain the SH genomes. Elymus arizonicus has been correctly classified.Key words: genome, meiosis, chromosome pairing, cytology, interspecific hybridization, Elymus, Agropyron, and Triticeae.


Sign in / Sign up

Export Citation Format

Share Document