The controlled introgression of Festuca arundinacea genes into Lolium multiflorum

Summary Using phosphoglucoisomerase (PGI/2) as a genetic marker, it has been shown to be possible to transfer genes from Festuca arundinacea into diploid Lolium multiflorum using the pentaploid hybrid L. multiflorum (4x) x F. arundinacea (6x). The pentaploid hybrid was sufficiently fertile to be used in reciprocal crosses with diploid. L. multiflorum. When used as the male parent, only two backcross generations were then required to reconstitute the diploid genotype. Intergeneric recombinants including a F. arundinacea PGI/2 allele were found among the diploid BC₂. Cytological data indicates that although the majority of chromosome associations involve only homologous Lolium chromosomes, associations involving Lolium and Festuca chromosomes also occur.Interpollinating the pentaploid hybrids prior to commencing a backcrossing programme increases the number of cycles of recombination and improves the chance of recovering intergeneric recombinants. The crossing programme described is proposed to be an effective method of introducing F. arundinacea genes into L. multiflorum.     

Cytogenetic study of Helianthus laevigatus and its F1 and BC1F1 hybrids with cultivated sunflower, Helianthus annuus

Although the wild sunflower species Helianthus laevigatus has not been extensively studied it may be considered for sunflower breeding as a potential source of desirable genes for Sclerotinia stalk rot resistance and high contents of proteins and linoleic acid in the seed. A set of six H. laevigatus populations was crossed to cultivated sun~ower lines and produced nine F₁ (2-14 plants) and 66 BC₁F₁ hybrid combinations (1-13 plants). Male sterility occurred in F₁ and BC₁F₁ hybrid combinations and pollen viability was lower in the progenies than in the parents (51.6-77.2%in F₁ and in F₁ and 4.8-34.0% in BC₁F₁). Meiosis was normal in the H. laevigatus populations It was found that this tetraploid species also occurred in a hexaploid form Numerous irregularities were observed in the meiosis of the F₁ interspecific hybrids During diakinesis, quadrivalents and hexavalents were recorded in addition to bivalents Dislocated chromosomes and chromosome bridges were present in the other phases The chromosome number in F₁ was 68 (tetraploid). Irregularities in chromosome pairing were observed in the interspecific hybrids at BC₁F₁. There were many univalents, and trivalents quadrivalents and hexavalents were also present The chromosome number in the BC₁F₁ generation ranged from 34 to 60. The occurrence of meiotic irregularities in the F₁ and BC₁F₁ interspecific hybrids indicates that H. laevigatus and the cultivated sunflower differ in genome constitution.     

Introgression of crown rust resistance from Festuca spp. into Lolium multiflorum

Crown rust, Puccinia coronata Corda, causes one of the most damaging foliar diseases in Italian ryegrass, Lolium multiflorum Lam. For introgression of crown rust resistance, highly resistant hybrids of the crosses Festuca arundinacea (2n = 6x = 42) ×L. multiflorum (2n = 4x = 28) and reciprocally, L. multiflorum (2n = 2x = 14) ×Festuca pratensis (2n = 4x = 28) and subsequently resistant recombinant individuals were used as female parents and susceptible cultivars of Italian ryegrass as male parents in three successive backcrosses. The BC₃ plants were selfed and crossed mutually. Uredospores of seven different crown rust isolates collected from plants of L. multiflorum, Lolium perenne, F. pratensis, F. arundinacea and L. multiflorum × F. pratensis hybrids were applied to identify the resistance or susceptibility of the parental species, backcrossed, selfed and intercrossed progenies. The various crown rust populations revealed a species-specific capability to infect plants of the Lolium-Festuca complex corresponding to the host species from which the spores originated. Selected BC⁹ plants, however, were found to be completely resistant to all crown rust populations tested. Successful introgression of the resistance was achieved from F. arundinacea as well as from F. pratensis. The resistance represents a dominant character, apparently based on a strong heterologous incompatibility between host and pathogen. In phenotype, bivalent formation during meiosis and in fertility, the novel germplasms are comparable with the L. multiflorum cultivars.     

Determination of the frequencies of restorer- and maintainer-alleles involved in CMS1 and CMS2 in German chive varieties

There are two cytoplasmic male sterility (CMS)‐systems in chives (Allium schoenoprasum L.), which can be employed in hybrid breeding. However, the probability for selection of maintainer genotypes from German open pollinated varieties is not known. Therefore, the allelic frequencies of the restorer genes X and T involved in CMS¹ were determined in 12 German commercial chive varieties by test crossing single plants to male sterile, temperature‐insensitive genotypes [(S₁)xxT] for segregation analyses of offspring. Temperature sensitive genotypes [(S₁)xxT_] are able to produce pollen at higher temperatures, and should therefore be excluded from hybrid breeding to avoid self‐pollination of the maternal parent. The mean value of the frequency of the non‐restoring allele x in the populations examined was 0.62. The mean value of the allele t, which is responsible for the temperature insensitivity, was 0.9. As a consequence of these allelic frequencies about one‐third of all plants of the chive varieties examined were designated CMS₁ maintainer genotypes, leading to the production of temperature insensitive male sterile lines. The incidence of CMS₂ maintainers in the German varieties examined was nearly four times lower than CMS₁ maintainers. The mean value of the frequency of the non‐restoring allele _st2 involved in the CMS₂‐system was 0.29.     

The transfer of triazine resistance from Brassica napus L. to B. oleracea L. II. Morphology,fertility and cytology of the F1 hybrid

Summary F₁ hybrids of triazine resistant Brassica napus and triazine susceptible B. oleracea were morphologically intermediate to the parent species. Of 49 hybrids examined, 44 had 28 chromosomes, two had 37, one had 38 and two had 56. The 38-chromosome plant was thought to be a matromorph, the others, A₁C₁C (28), A₁C₁CC (37) or A₁A₁C₁C₁CC (56) type hybrids. Pollen stainability averaged 9.0% in the sesquidiploid, 32.0% in the tetraploids and 89.5% in the hexaploids. All the interspecific hybrids were resistant to 1.0×10^-4 mol L^-1 atrazine. The sesquidiploid hybrids produced gametes with chromosome numbers ranging from 9 to 17 and the tetraploid hybrid gametes had chromosome numbers from 15 to 22. Most hybrids produced self-seed. The partial fertility of these hybrids may permit their backcrossing to one or both parents.     

Apical Development and Growth of Barley under Different CO2 and Nitrogen Regimes

Increases in atmospheric carbon dioxide (CO₂) concentration have stimulated interest in the response of agricultural crops to elevated levels of CO₂. Several studies have addressed the response of C₃ cereals to CO₂, but the interactive effect of nutrient supply and CO₂ on apical development and spikelet set and survival has not been investigated thoroughly. Hence, an experiment was conducted in the greenhouse to evaluate the effect of high (700 μmol CO₂mol^?1 air) and low (400 μmol mol^?1) levels of atmospheric CO₂ on apical development, spikelet set and abortion, and pre- and post-anthesis growth in spring barley (Hordeum vulgare L.) grown under high N (0.3 g N pot^?1 before sowing ?1–0.11 g N pot^?1 week^?1) and low N (0.3 g N pot^?1) regimes. The plants were grown in 5 L pots. Development of spike was hastened due to CO₂ enrichment, and the C+ plants pollinated few days earlier than the C— plants. Carbon dioxide enrichment had no effect on date of ripening. Development of spike slowed following application of extra N, and plants pollinated 10 days later and matured 2 weeks later when compared with plants under low N. Carbon dioxide enrichment did not affect the number of spikelets at anthesis. Excess N decreased spikelet abortion and the increased maximum number of spikelets under both [CO₂]. Barley plants did not tiller when grown in low [CO₂] and low N. Increased endogenous IAA concentration in those plants, recorded three days before tillers appeared in other treatments, may have contributed to this. Carbon dioxide enrichment increased the C concentration of plants, but decreased the N concentration under high N regime. Both the C and N concentration of plants were increased under high N regime. Carbon dioxide enrichment increased the total dry matter of mature plants by 9 % under high N regime and by 21 % under low N regime. Under high [CO₂] increased kernel number on tiller spikes, and increased kernel weight both on main stem and on tiller spikes resulted in a 23 % increase in kernel yield under low N regime and 76 % increase in kernel yield under high N regime. The rate of N application influenced growth and yield components to a greater extent than CO₂ enrichment. At maturity, plant dry matter, kernel weight, the number of kernels per spike, and the number of spikes per plant were higher under high N regime than under low N regime. Long days (16 h), low light intensity (280 μmol m^?2s^?1), and at constant temperature of 20 °C high [CO₂] increased kernel weight and the number of kernels on tiller spikes under high and low N application rate, but did not increase the number of kernels on main stem spike, or the number of tillers or tiller spikes per plant.     

Production of 27-, 28-, and 56-chromosome apomictic hybrid derivatives between pearl millet (2n=14) and Pennisetum squamulatum (2n=54)

Summary An interspecific hybridization program designed to transfer gene(s) controlling apomixis from Pennisetum squamulatum Fresen. (2n=6x=54) to induced tetraploid (2n=4x=28) cultivated pearl millet, Pennisetum americanum (L.) Leeke resulted in four offtype plants, two with 27 chromosomes and two with 28 chromosomes. These plants were found among 217 spaced plants established from open-pollinated seed of an apomictic 21-chromosome polyhaploid (2n=21) plant derived from an apomictic interspecific hybrid (2n=41) between tetraploid pearl millet and Pennisetum squamulatum. It appeared that a 21- (or 20-) chromosome unreduced egg from the apomictic polyhaploid united with a 7-chromosome pearl millet (2n=2x=14) gamete to produce a 28- (or 27-) chromosome offspring. Meiotic chromosome behavior was irregular averaging from 3.60 to 4.05 bivalents per microsporocyte in the 27- and 28-chromosome hybrids. The 27- or 28-chromosome hybrids, like the 21-chromosome female parent, shed no pollen, but set from 1.8 to 28 seed per panicle when allowed to outcross with pearl millet. Progeny of the 28-chromosome hybrids were uniform and identical to their respective female parents, indicating that apomixis had been effectively transferred through the egg. In addition, a 56-chromosome plant resulting from chromosome doubling of a 28-chromosome hybrid was identified. Pollen was 68 per cent stainable and the plant averaged 2.3 selfed seeds per panicle. Chromosomes of the 56-chromosome plant paired as bivalents (x=10.67) or associated in multivalents. Three to nine chromosomes remained unpaired at metaphase I. Multiple four-nucleate embryo sacs indicated the 56-chromosome hybrid was an obligate apomict. The production of 27-, 28-, and 56-chromosome hybrid derivatives were the results of interspecific hybridization, haploidization, fertilization of unreduced apomictic eggs, and spontaneous chromosome doubling. These mechanisms resulted in new unique genome combinations between x=7 and x=9 Pennisetum species.     

Infection of Lolium and Festuca spp. by Drechslera siccans and D. Catenaria

Summary Drechslera siccans was the commonest of the species of this leaf spot pathogen found on single spaced plants of Lolium perenne at Aberystwyth. D. catenaria and D. dictyoides were also frequently isolated. A wide range of genotypes within the host species L. perenne, L. multiflorum, Festuca arundinacea and F. pratensis, and structural hybrids between F. arundinacea and L. multiflorum, were all equally susceptible to conidial infection by D. siccans in the glasshouse and showed similar development of leaf spot symptoms, even though Festuca spp. are not normally attacked in the field. However, when exposed to infection out of doors there was significant variation in resistance, both between species and often also between genotypes within the same species. As in so many other instances of fungal infection, tetraploidy appeared to confer a higher level of resistance. The degree of resistance of a F. arundinacea × L. multiflorum amphiploid and two succeeding backcross generations to L. multiflorum approximated to that of the more susceptible L. multiflorum parent. By contrast to D. siccans, when plants were inoculated with D. catenaria in the glasshouse, both intervarietal and intravarietal variation in leaf spot development was evident. Resistance to D. siccans appears to depend partly on a limitation of conidial production, and to D. catenaria on restriction of hyphal growth following infection, which may explain the relative discrepancies between field and glasshouse results. The implications for resistance breeding are discussed.     

Chromosomal Stability in the Backcross Progenies of Pentaploid Hybrids between Avena sativa L. and A. maroccana Gdgr.

In a backcrossing programme to transfer desirable characters from wild Avena maroccana Gdgr. to cultivated oats, A. sativa L., meiotically stable plants in BC₁F₃ and BC₂F₂ progenies were isolated. The recovery of stable genotypes with 2n = 6×= 42 chromosomes indicated that two backcrosses are enough for such a programme. The cytological observations in various backcross generations are presented and discussed.     

Photosynthetic Acclimation and Productivity of Mungbean Cultivars under Elevated CO2 Concentration

Mungbean [Vigna radiata (L.) Wilczek] cultivars (Pusa Baisakhi, PS 16 and P 105) were grown in field at atmospheric (360 ± 10 ppm, AC) and elevated CO₂ (650 ± 50 ppm, EC) concentrations inside open top chambers for entire period of growth and development till maturity. Leaf net photosynthesis rate (P_N) of AC and EC grown plants when compared at same CO₂ concentration showed no significant down‐regulation of P_N in EC plants. In cv. P 105, even up‐regulation of P_N was observed in EC plants. Mungbean cultivars accumulated assimilates in the leaves during the day mostly in the form of starch. Nodule number and weight were also higher in EC plants. The positive effect of elevated CO₂ on P_N, dry‐matter production and seed yield was better expressed in cv. P 105 having greater podding ability.     

Unreduced gamete in interspecific hybrids in the Festuca/Lolium complex

Self-sterile interspecific hybrids between diploid Lolium perenne and either Festuca arundinacea or F. gigantea (both hexaploids) set some seeds when subjected to a heavy pollen cloud from the amphiploids derived from the hybrids. All the progeny were octoploid and were formed from the fertilization of unreduced gametes in the F₁ hybrid by amphiploid pollen. The significance of the results in relation to breeding efforts within the Lolium/Festuca complex is discussed.     

Heterosis for yield and other agronomic traits of winter triticale F1 and F2 hybrids

Triticale is generally treated as a self‐pollinating crop and line breeding is practised. Hybrid breeding has been discussed for some time, but there is little information for winter triticale. This study investigated heterosis for eight agronomic traits in F₁ and F₂ hybrids grown together with their parents as drilled plots in three environments. On average, grain yield heterosis was 12.5 dt/ha (a relative 10.5%) compared with the mid‐parent value for F₁ hybrids, and 6.2 dt/ha (5.0%) for F₂ hybrids and withawide range of 4.4–17.1 dt/ha for F₁ hybrids. A positive contribution to the heterosis of yield was made by kernels/spike and 1000‐kernel weight, whereas spikes/m² showed negative heterosis. Hybrid plants in F₁ and F₂ were taller than mid‐parents (8.3 cm and 5.3 cm, respectively), with a tendency to earlier heading. The negative heterosis for falling number in F₁ and F₂ hybrids could be a problem for commercial production of triticale hybrids. By selecting parents for combining ability and the identification of heterotic patterns, grain yield heterosis of 20% appears feasible.     

Androgenesis from a Lolium multiflorum × Festuca arundinacea hybrid to generate extreme variation for freezing-tolerance

New opportunities for plant breeding using androgenesis in Lolium × Festuca hybrids have been identified. Plants derived by anther culture from a Lolium multiflorum × Festuca arundinacea (5x) hybrid were screened for freezing-tolerance, and their post-freezing recovery compared. The androgenic population showed extreme diversity in freezing-tolerance. While the majority of androgenic plants had inferior freezing-tolerance compared with the freezing-sensitive L. multiflorum parent, 6% of the population were more freezing resistant than the freezing-tolerant Festuca parent. Novel Lolium and Festuca gene combinations resulting from rare meiotic events were recovered within the androgenic population. The two most freezing-tolerant androgenic plants carried virtually the entire F. pratensis subgenome of F. arundinacea. F. pratensis is known to carry genes for freezing-tolerance and would be expected to be the primary source of genes governing this trait within the F. arundinacea genome. The most freezing-tolerant androgenic plants were more freezing-tolerant than the hybrid plant from which they were derived. Consequently, androgenesis was also effective in removing factor(s) reducing the expression of freezing-tolerance within the L. multiflorum × F. arundinacea (5x) hybrid.     

Performance Studies in F6 Lines of Autotetraploid Fenugreek

Hybridization followed by pedigree selection was carried out between two autotetraploid strains of fenugreek (Trigonella foenum-graecum L.). Morphological and cytological investigations were carried out in two autotetraploid parents, their F₁ hybrids and F₆ lines derived from F₁ after selfing. Cytomorphological data of F₆ lines were compared with those of F₁, hybrids and of their parents. The hybrid plants were intermediate with respect to different vegetative traits, however, they showed increased seed set as compared to their autotetraploid parents. The mean pod number per plant in F₆ was one and half times as high as one of the high yielding tetraploid parents and approximately twice as high as that of F₁ hybrid. Meiosis in F₆ was more regular than in F, and the parents. Thus, hybridization followed by pedigree selection is helpful not only in regularizing the meiotic behavior, but vigour and seed fertility have also improved in autotetraploid fenugreek.     

Cytogenetic Studies of Hybrids between Festuca gigantea Vill. and Lolium multiflorum Lam.

The meiotic behaviour of the hybrid between Festuca gigantea (2n – 6x = 42) and Festuca gigantea (2n = 6x = 42) indicates distinct structural differences between the two species. These differences are also apparent in the degree of chromosome pairing observed in Lolium multiflorum×F. gigantea compared with previous reports on the L. multiflorum×F. arundinacea hybrids. Although the L. multiflorum×F. gigantea 8x amphiploid com Dines the complementary characters of the two species and is agronomically interesting, there are some irregularities in meiotic behaviour that could affect the stability of the amphiploid. Seed fertility in the amphiploid is high and preliminary studies show evidence of a high degree of self-fertility. The pentaploid hybrid between autotetraploid L. multiflorum×F. gigantea is sufficiently fertile to be used as the pollen plant in crosses with diploid L. multiflorum (BC₁). Backcrossing the BC₃ hybrid to L. multiflorum results in mainly diploid progeny. The possibilities, of using this crossing scheme to introgress F. gigantea characters into L. multiflorum is discussed as an alternative approach to amphiploid breeding as a means o: combining specific complementary characters of the two species.     

A Dominant Inhibitor Gene Inhibits the Expression of Ht2 against Exserohilum turcicum Race 2 in Corn Inbred Lines Related to B14

The purpose of this study was to elucidate the genetic cause for the lack of express ion of the gene Ht2 against Exserohilum turcicum race 2 on certain genetic backgrounds related to the inbred line B14. Two such inbreds (A635Rp and B59), susceptible to this pathogen were crossed onto the inbred Oh43—-Ht2Ht2. The following generations: F₁, F₂, F₃, F₄, backcrosses to both parents, selfings of the backcrosses, in addition to the parent lines, were evaluated for Ht2 expression in this study. Plants of each generation were inoculated with E. turcicum race 2 and evaluated for the expression of the chlorotic-lesion resistance determined by the gene Ht2. In spite of the reported dominance of Ht2 on some genetic backgrounds, the F₁ generations studied here did not show Ht2 resistant lesions. The data presented herein suggest that B₁₄ and related inbred lines carry a dominant gene(I) that inhibits the expression of the Ht2 gene. Chi-square analyses of the reactions of 108 progeny families studied supported this hypothesis.     

Performance of S2 Winter Barley Progenies from Original and Improved Populations Developed via Recurrent Selection

The effect of recurrent selection procedure for improving grain yield in autogamous cereals was evaluated in a six-rowed winter barley population. Gain from selection was estimated by field testing 90 random S2 lines from each of the C₀, C₁ and C₂ populations. Response to selection for grain yield was 0.78 t/ha from C₀ to C₁ and 1.09 t/ha from C₁ to C₂. Broad-sense heritability and genotypic variance for grain yield remained high in all cycles which suggests further gain from additional selection cycles. Yield increase was due to a higher number of seeds/m2. Significant differences among mean values were observed for heading date (189 days in C₀ and 182 days in C₂), whereas no variation was seen for plant height and 1000-kernel weight. The proposed recurrent selection procedure appears effective to improve the population and to extract superior genotypes for varietal development.     

Transfer of resistance to race 2 of Plasmodiophora brassicae from Brassica napus to cabbage (B. Oleracea spp. Capitata). IV. A resistant 18-chromosome B1 plant and its B2 progenies

Summary The somatic karyotype and meiotic chromosome behavior were studied in an 18-chromosome B₁ plant derived from backcrossing a triploid (Brassica napus x B. oleracea ssp. capitata) F₁ hybrid to cabbage. It is considered that cabbage chromosomes no. 1 and no. 7 were substituted by two shorter B. napus chromosomes. Meiotic disturbances were more apparent during the late stages of second division. Seed fertility of this plant was largely restored in the second backcrosses with both cabbage and broccoli. 18-chromosome B₂ plants resistant to race 2 of Plasmodiophora brassicae were recovered among the progenies.Contribution no. J. 725 from the Research Station, Research Branch, Agriculture Canada, St-Jean, Québec J3B 6Z8.     

Identification and characterization of genomic DNA sequences of the S-ribonuclease gene associated with self-incompatibility alleles S1 to S5 in European pear

The stylar products of the S‐locus for the gametophytic self‐incompatibility (GSI) system in the Rosaceae are ribonucleases (S‐RNases). Recently, sequences for 13 pear S‐RNase alleles have been published and named following a letter–symbol nomenclature (S_a to S_d and S_h to S_p). To establish the correspondence between these sequences and the self‐incompatibility alleles we have described previously (S₁ to S₅), we have amplified genomic DNA with consensus primers from the cultivars, ‘Williams’ (S₁S₂), ‘Coscia’ (S₃S₄), ‘Butirra Precoce Morettini’ (S₁S₃), ‘Santa Maria Morettini’ (S₂S₃) and ‘Doyenne du Comice’ (S₄S₅) and identified PCR products specifically associated with each S allele. Cloning and sequencing of the amplification products has revealed that they correspond to European pear sequences already deposited in the database. This allowed us to link S‐RNase sequences with S allele phenotypes and to determine a correspondence between the symbol–letter nomenclature used to name S‐RNase sequences and the number‐based nomenclature used to name S alleles. Based on this result the prediction of new cross‐incompatibilities among pear cultivars is discussed. Finally, we propose a unified number‐based nomenclature to avoid future confusion denominating S alleles in pear.