A new approach for obtaining rapid uniformity in rice (Oryza sativa L.) via a 3x x 2x cross

A triploid (2n = 3x = 36) rice plant was obtained by screening a twin seedling population in which each seed germinated to two or three sprouts that were then crossed with diploid plants. One diploid plant was chosen among the various F(1) progenies and developed into an F (2) population via self-pollination. Compared with the control variety Shanyou 63, this F (2) population had a stable agronomical performance in field trials, as confirmed by the F-test. The stability of the F (2) population was further substantiated by molecular analysis with simple sequence repeat markers. Specifically, of 160 markers assayed, 37 (covering all 12 chromosomes) were polymorphic between the parental lines. Testing the F (1) hybrid individually with these markers showed that each PCR product had only a single band instead of two bands from each parent. The bands were identical to either maternal (23 markers) or paternal (eight markers) bands or distinct from both parents (six markers). The amplified bands of all 60 randomly selected F (2) plants were uniform and identical to those of the F (1) hybrid. These results suggest that the F (1) plant is a non-segregating hybrid and that a stable F (2) population was obtained. This novel system provides an efficient means for shortening the cycle of hybrid rice seed production.     

Characterisation of progeny from backcrosses of triploid hybrids between Hordeum vulgare L. (2x) and H. bulbosum L (4x) to H. vulgare

Interspecific hybridisations between Hordeum vulgare L. (cultivated barley) and H. bulbosum L. (bulbous barley grass) have been carried out to transfer desirable traits, such as disease resistance, from the wild species into barley. In this paper we report the results of an extensive backcrossing programme of triploid hybrids (H. vulgare 2x x H. bulbosum 4x) to two cultivars of H. vulgare. Progenies were characterised cytologically and by restriction fragment length polymorphism analysis and comprised (1) haploid and diploid H. vulgare plants, (2) hybrids and aneuploids, (3) single and double monosomic substitutions of H. bulbosum chromosomes into H. vulgare and (4) chromosomal rearrangements and recombinants. Five out of the seven possible single monosomic chromosome substitutions have now been identified amongst backcross progeny and will be valuable for directed gene introgression and genome homoeology studies. The presence amongst progeny of 1 plant with an H. vulgare-H. bulbosum translocated chromosome and one recombinant indicates the value of fertile triploid hybrids for interspecific gene introgression.     

Cultivar x environment interactions in sorghum,Sorghum bicolor (L.) moench

Summary The most significant and important interactions in 2, and 3-year sorghum zonal trials were location x year, cultivar x location and cultivar x location x year. Cultivar x year interaction was significant in one out of four ecologic zones used in the trials. The variance components were relatively small with the second order interaction variance component larger than the first order types involving cultivars. Environmental variance was the largest in all four zones.Computations on theoretical standard error of cultivar means suggest that six replications, eight locations and four years is an ideal testing procedure in the Northern Guinea Savanna, while in the Sudan Savanna, the combination is better with four replications, eight locations and three years. The true value or performance of a variety is most effectively obtained by increasing the number of years, while increasing number of replications is the least effective.     

Synaptonemal complex formation in hybrids of Lolium temulentum x Lolium perenne (L.)

Comparisons were made between two kinds of tetraploids derived from the hybrid Lolium temulentum x L. perenne. One hybrid behaves like an autotetraploid with multivalents at first metaphase of meiosis in pollen mother cells. The other behaves like an allotetraploid, in which pairing at first metaphase is restricted to bivalents comprised of strictly homologous chromosomes. The diploidisation of the latter form is controlled by determinants located on both the normal, A chromosomes and on supernumary B chromosomes. Reconstruction of synaptonemal complexes and their elements, from serial sections through pollen mother cell nuclei examined under the electron microscope, reveals that at zygotene pairing in both forms results in multivalent formation involving non-homologous as well as homologous chromosomes. The mechanism responsible for the diploidisation is, therefore, not based on a restriction of pairing at early meiosis to homologous chromosomes but on a correction or transformation of the multivalent chromosome associations to bivalents subsequent to zygotene. The transformation is not completed until late pachytene. In the multivalent-forming tetraploid a maximum of four chromosomes are associated at first metaphase. Yet configurations of a higher valency are found at zygotene. There is, therefore, a partial transformation of multivalents even in this autotetraploid form which restricts configurations at metaphase I to homologous and homoeologous chromosomes only. In both hybrids some homologous bivalents are not the product of resolution of multivalents but result from two-by-two pairing from the beginning of zygotene.     

Extension of the Messapia x dicoccoides linkage map of Triticum turgidum (L.) Thell

A set of recombinant inbred lines (RIL) derived from a cross between the cultivar Messapia of durum wheat (Triticum turgidum var. durum) and the accession MG4343 of T. turgidum var. dicoccoides was analysed to increase the number of assigned markers and the resolution of the previously constructed genetic linkage map. An updated map of the durum wheat genome consisting of 458 loci was constructed. These loci include 261 Restriction Fragment Length Polymorphisms (RFLPs), 91 microsatellites (Simple Sequence Repeats, SSRs), 87 Amplified Fragment Length Polymorphisms (AFLPs), two ribosomal genes, and nine biochemical (seven seed storage proteins and two isozymes) and eight morphological markers. The loci were mapped on all 14 chromosomes of the A and B genomes, and covered a total distance of 3038.4 cM with an average distance of 6.7 cM between adjacent markers. The molecular markers were evenly distributed between the A and the B genomes (240 and 218 markers, respectively). An additional forty loci (8.8%) could not be assigned to a specific linkage group. A fraction (16.4%) of the markers significantly deviated from the expected Mendelian ratios; clusters of loci showing distorted segregation were found on the 1B, 2A, 2B, 3A, 4A, 7A and 7B chromosomes. The genetic lengths of the chromosomes range from 148.8 cM (chromosome 6B) to 318.0 cM (chromosome 2B) and approximately concur with their physical lengths. Chromosome 2B has the largest number of markers (47), while the chromosomes with the fewest markers are 3A and 6B (23). There are two gaps larger than 40 cM on chromosomes 2A and 3B. The durum wheat map was compared with the published maps of bread and durum wheats; the order of most common RFLP and SSR markers on the 14 chromosomes of the A and B genomes were nearly identical. A core-map can be extracted from the high-density Messapia x dicoccoides map and a subset of uniformly distributed markers can be used to detect and map quantitative trait loci.     

Somatic hybrids and cybrids of Senecio fuchsii Gmel. (x) jacobaea L.

Summary In situ hybridisation and restriction fragment length polymorphism (RFLP) analysis were used to determine the relative location of the translocation breakpoint and the size of the integrated chromatin segment in hexaploid wheat-Lophopyrum translocation stocks. Three 7el₂-7D recombinant stocks were Robertsonian translocations, 7DS.7el. The remaining recombinant stock (KS10-2) was 7elS.7el-7DL and contained only the distal one-half of the long arm of 7D. The recombinant stock with 7el₁ (K11695) could be designated 7DS.7DL-7el where approximately the distal one-half of 7DL was replaced. RFLP analysis indicated that on the 7DL RFLP map the breakpoints for K11695 and KS10-2 are in different locations and that the two recombinants contain an overlapping region (a common region) of the Lophopyrum chromosome 7 in which Lr19, a leaf-rust resistant gene, is located. RFLP analysis also indicated that RFLP markers which mapped to within 1.5 cm of the centromere of chromosome 7D are located in the distal half of the long arm.     

Bumblebee death associated with Tilia x europaea L

For more than six decades, bumblebee death, which mainly occurs in August, has been assumed to be associated with intake of presumed toxic nectar from linden trees (Tilia spp.), a hypothesis which has been sustained by observations of a significant number of dead bumblebees under these trees during their flowering season. Several theories exist in current literature to account for these observations. The nectar has been assumed to contain compound(s) toxic to the bumblebees including the monosaccharide mannose, which cannot be metabolized by bumblebees. The presence of toxic compounds such as the alkaloid nicotine or pesticides of anthropogenic origin has also been indicated. However, none of the above suggested compounds have hitherto been properly characterized from the nectar. In the current paper we report on characterization of the composition of nectar of linden trees, under which a significant number of dead bumblebees were observed. The structure determinations were performed by selective 1D TOCSY NMR and extensive applications of 2D NMR spectroscopy. The nectar of the linden flowers was readily available in significant amounts during the entire period when dead bumblebees were observed under these trees. The nectar only contained non-toxic sugars such as α-glucopyranose, β-glucopyranose, sucrose, fructose and minor amounts of xylose. The nectar did not contain mannose, nor alkaloids or pesticides. Initial toxicity studies using brine shrimp lethality assay showed that the nectar did not exhibit any toxic effects even at concentrations higher than 1 mg/ml dry weight, providing disproving evidence against the assumption of the nectar's toxic character.     

Cytogenetic studies in Papaver L.; the x= 6 and x= 7 diploids

Although hybridization between species in Papaver is difficult, a combination of karyotypic and genomic analysis has allowed the definition of up to six, apparently independent genomes, in the 2n= 12 and 1n= 14 diploids. In the 2n= 14 group there is considerable karyotypic differentiation and karyotypes off. atlanticum and P. hybridum are sufficiently dissimilar from each other and from the rest to allow the recognition of the two genomes as unique although no hybrids with other x= 7 diploids were produced. The genome of P. atlanticum is defined as C₇C₇ and that of P. hybridum H₇H_7.P. alpinum and P. rhaeticum only hybridized successfully with each other and the near perfect bivalent formation in their hybrid, together with the extreme similarity of their karyotypes, suggests that they are very closely related. They are designated J₇J₇. All the other x=7 diploids are karyotypically similar and the analysis of meiosis in their hybrids demonstrates thay they all share the same genome to some extent. There is however some differentiation among them. P. commutatum, P. glaucum, P. macrostemum and P. rhoeas are genomically very similar and all can be regarded as A₇A₇. P.fugax and P. tauricola appear to share an identical genome, partially differentiated from A₇A₇ and are defined as A²₇A²₇ while P. postii, although showing some little homology with A₇A₇ is sufficiently differentiated from it to be regarded as more distant than A²₇A²₇ and is described as A³₇A³₇. Although no hybrids between the two 2n= 12 diploids P. apulum and P.pavoninum were produced their karyotypes are sufficiently different to be individually recognized. The only hybrid produced between the x= 6 and x= 7 groups (P. apulum×P. hybridum) showed no homology between the chromosomes of the two genomes and, although this may not be true for any other x=6/x=7 combinations it is best to recognize the two x= 6 genomes as independent of the x= 7. The genome of P. apulum is thus regarded as I₆I₆ and that of P. pavoninum as P₆P₆.     

Line x tester analysis for fixed effect model in cotton (Gossypium hirsutum L.)

Summary The data from an experiment in cotton consisting of three testers and 12 lines selected deliberately have been analysed. The investigation showed higher specific combining ability variance for yield of seed cotton and number of bolls, indicating the predominance of non-additive gene action. Of parental lines, H777 was found to possess high g.c.a. effects for seed cotton yield, number of bolls and number of sympodes. Parent H842 contributed only for boll weight, whereas H655 was good general combiner for number of monopodes. There appeared to be better chances for increasing the yield by exploiting hybrid vigour for the number of bolls and boll weight. The presence of marked non-additive gene effects, in addition to additive gene effects, indicated the need for exploiting both the fixable and non-fixable components of genetic variance for increasing productivity in cotton.     

Inheritance of organelle DNA in rye (Secale cereale L.) and wheat (x Triticale Thch.) hybrids

The mode of inheritance of chloroplast and mitochondrial DNA (mtDNA) in rye x triticale intergeneric hybrids has been studied with the use of specific PCR markers for loci 18S/5S and 3'rbcL in organelle DNA. In rye x triticale BC1, mtDNA copies of two types, paternal and maternal, have been found; in BC2 plants, only paternal mtDNA and chloroplast DNA (cpDNA) have been detected. Mechanisms determining the inheritance and/or differential amplification of organelles of a specific type are discussed.     

Chromosome numbers,characterization of chromosomal pairing during meiosis,origin and natural propagation in polyploid cytotypes (4x, 5x and 6x) of Agrimonia eupatoria L. (Rosaceae) in northwest Himalayas (India)

Despite the presence of intraspecific polyploidy (2x, 4x, 5x and 6x) in Agrimonia eupatoria, origin of these cytotypes has never been addressed adequately. The aim of the present study was to record the original chromosome counts and characterize chromosomal pairing during meiosis and microsporogenesis in the 5x cytotype, and discussing the hypothesis regarding the possible origin of polyploid cytotypes (4x, 5x and 6x) in the species. The geographical distribution pattern of cytotypes in the Indian Himalayas and elsewhere has also been analyzed. The present meiotic analysis revealed three chromosomes counts, the tetraploid (2n?=?4x?=?56), the pentaploid (2n?=?5x?=?70) and the hexaploid (2n?=?6x?=?84) cytotypes based on x?=?14. Meiotic course was perfectly normal in the 4x and 6x cytotypes resulting into high pollen fertility (94–100 %). Meiotic course in the imbalanced 5x cytotype has been found to be irregular characterized by the presence of high frequency of univalents at diakinesis and metaphase-I. Abnormal meiotic course contributed towards high pollen sterility (74–88 %). Even the apparently fertile/stained pollen grains were of irregular shape and of heterogeneous sizes. Meiotic behaviour of the 5x cytotype is like typical of allopolyploid. Individuals of 5x cytotype did not produce seeds and propagate vegetatively (root suckers) while 4x and 6x cytotypes exploited sexual (seeds) as well as vegetative means for propagation. Chromosomal pairing in pentaploid cytotype is like typical of an allopolyploid and we assume that it might have originated owing to natural inter-cytotype hybridization between 4x and 6x cytotypes in a mixed population. Analysis of geographical distribution pattern of cytotypes shows that Indian Himalayas represent the most cytotype-diverse region for A. eupatoria with the existence of all the four cytotypes (2x, 4x, 5x, 6x). This shows the dynamic nature of the species at chromosomal level in this part of the world.     

Central cell nuclear-cytoplasmic incongruity:a mechanism for segregation distortion in advanced backcross and selfed generations of (Allium cepa L. x Allium fistulosum L.) x A. cepa interspecific hybrid derivatives

A model is presented as an explanation for an anomaly observed in germination and establishment and isozyme segregation patterns in Allium cepa x A. fistulosum F2BC3 populations generated in an introgression-breeding program. The F1BC3 parent of these populations was selected for its heterozygous PGI phenotype, Pgi-1(2/3); Pgi-1(2) was inherited from an A. cepa (Ac) seed parent and Pgi-1(3) from an A. fistulosum (Af) pollen parent. Germination and establishment was recorded for the F2BC3 progeny population. Segregation of Ac and Af Pgi-1 alleles was investigated in F2BC3 seeds and embryo and endosperm tissue was isolated and tested for isozyme expression. A pooled goodness-of-fit test of the segregation of Pgi-1 alleles in the populations to the expected Mendelian 1:2:1 ratio using the chi-square statistic gave a chi2 = 185.9, well beyond the accepted limits at 2 degrees of freedom. The 1:2:1 ratio expected for simple Mendelian inheritance was rejected, while a pooled chi-square goodness-of-fit test of the segregation of Pgi-1 alleles in the populations fit a 1:1 ratio with a chi2 = 0.203, based on the incongruity model. We present here the central cell nuclear-cytoplasmic incongruity hypothesis to explain the observed anomalies.     

Investigation of some yield and fibre quality characteristics of interspecific hybrid (Gossypium hirsutum L. x G. barbadense L.) cotton varieties

Interspecific hybrid cottons (Gossypium hirsutum L. x G. barbadense L.) have great both yield and quality potential. This study was conducted to determine potential yields and quality characteristics of hybrid cotton varieties in southeastern Anatolia region of Turkey. The experiment was set out a completely randomized block design with four replications during 2003 and 2004 at University of Dicle, Faculty of Agriculture Experimental Field. Seven interspecific hybrid cotton varieties (48-08, Sevilla, Europe, Ica, Etna, 14-08 and Acalpi) which were obtained from Israel, and commonly grown varieties in this region, non-hybrid cotton varieties, GW Teks and DP-Opal were used as the materials of the study. Difference among the cultivars was significant for all traits except sympodial branch. Maximum number of boll and lint yield was 20.18 n plant(-1) and 1685.8 kg ha(-1) from interspecific hybrid cotton Ica, while interspecific hybrid cotton Europe recorded the lowest number of boll and lint yield. Interspecific hybrid cotton varieties showed higher value for fibre length, fibre fineness and fibre strength than non-hybrid cotton varieties. The longest fibres were obtained from Acalpi and Etna (34.08 and 33.88 mm), while non-hybrid varieties, DP-Opal and GW-Teks, had the lowest fibre length, 28.50 and 30.03 mm, respectively. The finest fibres obtained from Ica and 48-08 (3.42 and 3.45 mic.), the strongest fibres from Etna and Acalpi (40.07 and 40.23 g tex(-1)), and most elongation fibres from Acalpi (8.00%) and Sevilla (7.45%). Lint yield correlated positive and significant with fiber length.     

上位性和QTL×环境互作对水稻(Oryza sativa L.)抽穗期的影响

水稻抽穗期是重要的农艺性状之一,对水稻品种的地理分布和适应性起到关键性作用。适宜的抽穗期是获得高产的前提。因此确定水稻抽穗期的遗传基础在育种计划中具有重要的意义。本研究用一套来源于亲本IR64/Azucena的双单倍体（DH）群体在两个种植季节的试验资料,用基于混合线性模型的复合区间作图方法,对水稻抽穗期QTL的加性、上位性及其与环境互作效应进行了研究。结果表明共有14个QTL影响水稻抽穗期,它们分布在除第5和第9条染色体外的10条染色体上,有8个位点携带单位点效应,5对位点携带双位点互作效应,2个单位点和1对双位点存在与环境的互作,所有效应值介于1.179～2.549天之间,相应的贡献率为1.04%～4.84%。基于所估算的QTL效应值,本研究预测了两个亲本和两个极端型品系的遗传效应值,并讨论了影响遗传效应值与实际观测值偏差的可能原因,以及研究群体所具有的遗传潜力。对水稻抽穗期QTL的定位结果与前人研究基本一致,并进一步证实了上位性和QE互作效应是水稻抽穗期的重要遗传基础。     

Somatic embryogenesis and plant regeneration from protoplasts of Cichorium intybus L. x Cichorium endivia L.

Somatic embryos and adult plants were regenerated from mesophyll protoplasts of a clone of chicory 474 (Cichorium intybus L. x Cichorium endivia L.). Embryos were obtained in three different ways:

A comparative map of wild rice (Zizania palustris L. 2n=2x=30)

We present the first genetic map of wild rice (Zizania palustris L., 2n=2x=30), a native aquatic grain of northern North America. The map is composed principally of previously mapped RFLP (restriction fragment length polymorphism) genetic markers from rice (Oryza sativa 2n=2x=24). The map is important as a foundation for genetic and crop improvement studies, as well as a reference for genome organization comparisons among Gramineae species. A comparative mapping approach with rice is especially useful because wild rice is grouped in the same subfamily, Oryzoideae, and no other mapping comparison has yet been made within the subfamily. As rice is the reference point for mapping and gene cloning in cereals, establishing a consensus map within the subfamily identifies conserved and unique regions. The genomes of wild rice and rice differ in total DNA content (wild rice has twice that of rice) and chromosome pairs (wild rice=15 versus rice=12). The wild rice linkage map reported herein consists of 121 RFLP markers on 16 linkage groups spanning 1805 cM. Two linkage groups consist of only two markers. Colinear markers were found representing all rice linkage groups except #12. The majority of rice loci mapped to colinearly arranged arrays in wild rice (92 of 118). Features of the map include duplication of portions of three rice linkage groups and three possible translocations. The map gives basic information on the composition of the wild rice genome and provides tools to assist in the domestication of this important food source. Received: 25 August 1998 / Accepted: 20 February 1999 (Corrected version. Originally published in TAG 99:793–799)