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In the presented hybridization programme of barley cultivars and rye inbred lines including 48 cross combinations the seed set ranged from 3.13 to 92.98%, while embryos were formed in 0.74 to 36.36% in successful pollinations. Sixty five plants were generated by embryo callus culture and one - by embryo culture without callus formation. The hybrids had somatic chromosome numbers 2n=14 (60 plants) and 2n=28 (6 plants). Plants obtained via embryo callus culture showed good vegetative vigour and well-developed root system. Spike morphology of all plants resembled that of rye. Meiosis in 17 diploids showed 0.13-0.63 barley-barley and rye-rye bivalents with a chiasma frequency of 0.14-0.69 per cell. The heteromorphic bivalent-like configurations occurred in five plants in 0.01-0.02 per cell. The amphidiploids had 7.79-10.71 barley-barley and rye-rye bivalents with a chiasma frequency of 9.36-17.75 per cell. All plants, with 14 and 28 chromosomes, were completely sterile both in backcrosses and when selfed.
In the years 1964-1994 an extensive programme of wide hybridization within Ihe. Lolium-Festuca complex was carried out in Poland. Six Lolium (ryegrass) and five Festuca (fescue) species at different ploidy level were used for crosses. Hybrids were obtained from 72 cross combinations: 19 interspecific (five Lolium × Lolium and 14 Festuca × Festuca), 51 intergeneric (39 Lolium × Festuca and 12 Festuca × Lolium) and two trispecific (Lolium × Festuca × Festuca), most of them being derived from crosses of four important forage grass species: Lolium multiflorum, L. perenne, Festuca pratensis and F. arundinacea. Interspecific and intergeneric Lolium-F estuca hybrids from 50 cross combinations are maintained at present in the collection of the Institute of Plant Genetics in Poznań. This article presents a complete list of Lolium-Festuca hybrids obtained in Poland in the years 1964-1994 and maintained in the collection. The available literature concerning these hybrids is cited.
Amphiploid pollen of Aegilops kotschyi x Secale cereale was compared to the parental form by SEM, and comparatively measured using light microscopy. Pollen grains of amphiploids were larger and more variable in total and pore diameter than the parents. Amphiploid pollen was prolate, subprolate and prolate-spheroidal in shape. The exine of Ae. kotschyi AK-2 and AK-3 had a delicate verrucate surface, whereas Secale cereale S14 exine had a verrucate surface. Amphiploid pollen grain surfaces were more or less similar to those of the parents: delicate verrucate, verrucate and well verrucate. The sculpture of parental and amphiploid pollen grains showed conspicuous granulation. All amphiploids produced pollen with one pore with an operculum, surrounded by a well-defined annulus. Sporophytically produced peptides from the pollen coat and gametophytically produced peptides from the protoplast were analyzed separately by two-dimensional gel electrophoresis. Two accessions ofAe. kotschyi (AK-2, AK-3) showed differences in the 2-D patterns of peptides from both the pollen coat and the protoplast. The majority of pollen coat and protoplast peptides of the parents were detected in the amphiploids, but a number of parental peptides were absent. All the amphiploids possessed peptides in their pollen coat and protoplast not detected in the corresponding pollen fractions of the parents. No relation between colchicine and in vitro amphiploid production and its 2-D patterns was observed. The results of pollen morphology and pollen protein analysis are convergent.
Genomic in situ hybridisation (GISH) was used to reveal chromosome pairing in two partly fertile, triploid (2n = 3x = 21) hybrids obtained by crossing the diploid (2n = 2x = 14) Festuca pratensis Huds. (designated FpFp), used as a female parent, with the autotetraploid (2n = 4x = 28) Lolium multiflorum Lam. (designated LmLmLmLm), used as a male parent. The pattern of chromosome pairing calculated on the basis of the mean values of chromosome configurations identified in all 100 PMCs analysed, was: 0.71I Lm + 2.24I Fp + 2.18II Lm/Lm + 0.54II Lm/Fp + 4.18III Lm/Lm/Fp. A relatively high number of Lm/Lm bivalents and Fp univalents, and a low number of Lm/Fp bivalents and Lm univalents indicated that the pairing was preferential between L. multiflorum chromosomes. Other observations regarding chromosome pairing within the Lm/Lm/Fp trivalents also confirmed this preferential pairing in the analysed triploids, as the Fp chromosome was not randomly located in the chain- and frying-pan-shaped trivalents. The similarities and differences in chromosome pairing at metaphase I and the level of preferential pairing between Lolium chromosomes in the different triploid Lolium-Festuca hybrids are discussed.
Systematyczne gromadzenie materiałów kolekcyjnych pszenżyta rozpoczęto w 1982 roku. Początkowo gromadzono głównie rody hodowlane otrzymane w krajowych ośrodkach hodowli pszenżyta. Następnie sprowadzono materiały ze światowych banków genów: Beltsville, Gatersleben, VIR. Do kolekcji włączono także interesujące materiały mieszańcowe otrzymywane w placówkach badawczych. Obecnie kolekcja liczy 2333 obiektów, w tym 1339 pszenżyta ozimego i 994 pszenżyta jarego. Waloryzacja prowadzona jest w 4-letnim cyklu doświadczeń potowych według jednolitej metodyki. Zgromadzone materiały kolekcyjne reprezentują duże spektrum zmienności zarówno cech morfologicznych, jak i użytkowych. Duże zróżnicowanie badanych obiektów kolekcyjnych dotyczy zwłaszcza takich cech, jak: wysokość roślin, liczba i masa ziaren z kłosa, zawartość białka w ziarnie oraz potowej odporności na mączniaka właściwego i rdzę brunatną.
This study focuses on the variability of chromosomal location and number of ribosomal DNA (rDNA) sites in some diploid and autotetraploid Festuca pratensis and Lolium perenne cultivars, as well as on identification of rDNA-bearing chromosomes in their triploid and tetraploid F. pratensis × L. perenne hybrids. The rDNA loci were mapped using fluorescence in situ hybridization (FISH) with 5S and 25S rDNA probes, and the origin of parental genomes was verified by genomic in situ hybridization (GISH) with L. perenne genomic DNA as a probe, and F. pratensis genomic DNA as a block. FISH detected variation in the number and chromosomal location of both 5S and 45S rDNA sites. In F. pratensis mostly additional signals of 5S rDNA loci occurred, as compared with standard F. pratensis karyotypes. Losses of 45S rDNA loci were more frequent in L. perenne cultivars and intergeneric hybrids. Comparison of the F. pratensis and L. perenne genomes approved a higher number of rDNA sites as well as variation in chromosomal rDNA location in L. perenne. A greater instability of F. pratensis-genome-like and L. perenne-genome-like chromosomes in tetraploid hybrids was revealed, indicating gains and losses of rDNA loci, respectively. Our data indicate that the rDNA loci physically mapped on chromosomes 2 and 3 in F. pratensis and on chromosome 3 in L. perenne are useful markers for these chromosomes in intergeneric Festuca × Lolium hybrids.
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