Selection for economic characters in Lupinus angustifolius and L. digitatus. 2. Time of flowering

1969 ◽  
Vol 9 (37) ◽  
pp. 213 ◽  
Author(s):  
JS Gladstones ◽  
GD Hill
Keyword(s):  
Dark Period ◽  
Dominant Gene ◽  
Lupinus Angustifolius ◽  
Vernalization Requirement ◽  
Flower Initiation ◽  
Naturally Occurring ◽  
Sowing Dates ◽  
Selection For ◽  
Western Australian ◽  
Dominant Genes

Early-flowering plants were selected from a field population of Lupinus angustifolius and from field and X-ray-treated populations of L. digitatus. One naturally-occurring dominant gene for earliness was isolated in each species, together with an artificially-induced recessive, unlinked to the dominant, in L. digitatus. To evaluate the different genotypes for breeding purposes, and to analyse the factors of the Western Australian environment controlling their flowering time, sowings of all genotypes were made with and without artificial vernalization, over a range of sowing dates, and in a range of environments differing mainly in temperature. Effects on flower initiation were estimated from times of flowering and first flowering node numbers. Flowering of L. angustifolius was found to be controlled mainly by its vernalization requirement. In L. digitatus, vernalization, a dark period inhibition, and an acceleration of flower initiation by high temperatures all appeared to be important. The dominant genes of both species removed all effective vernalization requirement, while the recessive in L. digitatus may have removed or relaxed a dark period inhibition. It was concluded that all three earliness genes would be useful in extending the cultivation ranges of the two species.

Genotypic and environmental effects on pod wall proportion and pod wall specific weight in Lupinus angustifolius

2004 ◽  
Vol 55 (4) ◽  
pp. 397 ◽  
Author(s):  
M. Mera ◽  
C. Harcha ◽  
H. Miranda ◽  
J. L. Rouanet
Keyword(s):  
Seed Weight ◽  
Specific Weight ◽  
Lupinus Angustifolius ◽  
Southern Chile ◽  
Coefficients Of Variation ◽  
Genetic Level ◽  
Pod Wall ◽  
Selection For ◽  
Western Australian ◽  
Genotypic Effects

Fourteen winter-sown genotypes of Lupinus angustifolius L., comprising most of the Western Australian cultivars released since 1986, were studied over 2 years at 4 southern Chile locations. Pod wall proportion, pod wall specific weight, seed number per pod, mean seed weight, seed weight per pod, wall weight per pod, and mean pod weight were measured, separately sampling pods from the mainstem and pods from branches. The 2 pod positions differed significantly for all characteristics except wall weight per pod. Lower coefficients of variation and greater heritabilities for both pod wall proportion and pod wall specific weight were achieved with a sample of pods from branches than with a sample from the mainstem.The ranges for pod wall proportion and pod wall specific weight were small (31.8–35.8% and 27.0–34.7 mg/cm2, respectively); however, highly significant genotypic effects were found for both characters. Heritability estimates were moderate for pod wall proportion (0.27 and 0.44 for pods from mainstem and branches, respectively) and moderate to high for pod wall specific weight (0.56 and 0.61, respectively).Pod wall proportion and pod wall specific weight were significantly correlated, more so at the genetic level (rg�=�0.83 and rg = 0.76 for pods from mainstem and branches, respectively) than at the phenotypic level (rph = 0.57 and rph = 0.60, respectively). Pod wall specific weight was closely associated with wall weight per pod, meaning that larger pods call for thicker pod walls. Accordingly, selection for low pod wall specific weight in a breeding program could lead to light pods. Correlations with mean seed weight indicate that this trait could decrease as well.

Mapping a gene conferring resistance to Pseudocercosporella herpotrichoides on chromosome 4V of Dasypyrum villosum in a wheat background

Genome ◽  
1998 ◽  
Vol 41 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Ahmet Yildirim ◽  
Stephen S Jones ◽  
Timothy D Murray
Keyword(s):  
Distal Part ◽  
Dominant Gene ◽  
Rflp Markers ◽  
Addition Line ◽  
Dasypyrum Villosum ◽  
Pseudocercosporella Herpotrichoides ◽  
Eyespot Resistance ◽  
Double Recombination ◽  
Simultaneous Selection ◽  
Selection For

The objectives of this study were to map and tag the previously undescribed eyespot resistance gene PchDv on chromosome 4V of Dasypyrum villosum in a wheat background. The 82 F2 plants used for mapping were produced from a cross between a susceptible\i wheat 'Yangmai-5' (4V(4D)) substitution line and a resistant wheat 'Chinese Spring' disomic addition line of chromosome 4V of D. villosum. Segregation for resistance and susceptibility among F2 plants was 3:1, indicating that resistance was controlled by a single dominant gene. PchDv mapped to the distal part of chromosome 4V and was bracketed by two RFLP markers, Xcdo949 and Xbcd588, in a 33-cM interval. This distance could not be reduced, owing to a lack of polymorphic loci in this region. Theoretically, double recombination in this region occurs in 3.3% of the individuals; therefore, 96.7% of the selected genotypes would have PchDv, with simultaneous selection for both flanking markers. Double recombination between the flanking markers was observed in 2 out of 82 (2.4%) F2 individuals.

scholarly journals The mechanism whereby the genes M1 and M2 in Paramecium aurelia, stock 540, control growth of the mate-killer (mu) particles

1962 ◽  
Vol 3 (1) ◽  
pp. 24-50 ◽  
Author(s):  
I. Gibson ◽  
G. H. Beale ◽  
E. C. R Reeve
Keyword(s):  
Recipient Cell ◽  
Physiological Activity ◽  
Dominant Gene ◽  
Initial Number ◽  
Irregular Distribution ◽  
Large Numbers ◽  
Control Growth ◽  
Phenotypic Manifestation ◽  
A Cell ◽  
Dominant Genes

1. Replacement of the dominant genes M1 and M2 in Paramecium aurelia, stock 540 (syngen/variety 1), results in loss of ability to maintain mu particles and manifestation of mate-killing after a delay of eight to fifteen fissions in most cells. The change, when it does occur, is relatively abrupt, extending over less than the space of one inter-fission period.2. The delay between change of genotype and loss of mu particles is interpreted as being due to presence in the initial cytoplasm of some thousand ‘metagons’, which are non-replicating gene derivatives having the physiological activity of the corresponding genes. During successive fissions of paramecia deprived of M1 and M2 the metagons are passively distributed amongst the progeny, until virtually all animals lack them.3. On reaching a stage at which some individuals of genotype m1m1m2m2 contain only a single metagon, the paramecia still contain large numbers of mu particles and are mate-killers. Fission of such animals gives rise to one daughter again with mu particles, and another in which the latter are destroyed during the next inter-fission period.4. By induced cytoplasmic exchange between conjugants, metagons can be transferred from one animal to another via the cytoplasm. Where such transference is into an animal not originally containing mu particles, that animal is converted into a condition in which it favours the maintenance of mu particles and transmits the latter to one or more of its offspring.5. Distribution of metagons amongst progeny of dividing paramecia is not random, due possibly to clumping of the metagons. Induced cytoplasmic exchange seems to break up the clumps.6. Reintroduction of a dominant gene (M2) into a cell recently deprived of the same gene, succeeds—even after fifteen fissions—in re-establishing the ability to support growth of mu particles, provided that the recipient cell contains at least one metagon and one or more mu particles. There is a regular lag of only one fission between introduction of such a dominant gene and its phenotypic manifestation.7. Mathematical formulae are developed for calculating the expected initial number of metagons, the proportions of animals lacking mu particles at each fission following loss of the dominant genes, and the proportions of cells containing 0, 1, 2 …, etc. metagons per cell at any stage. The consequences of one of the possible types of irregular distribution of metagons in dividing paramecia are also considered mathematically.

INHERITANCE OF CROWN RUST RESISTANCE IN THREE ACCESSIONS OF AVENA STERILIS

1980 ◽  
Vol 22 (1) ◽  
pp. 27-33 ◽  
Author(s):  
D. E. Harder ◽  
R. I. H. McKenzie ◽  
J. W. Martens
Keyword(s):  
Rust Resistance ◽  
Dominant Gene ◽  
Crown Rust ◽  
Inheritance Of Resistance ◽  
Single Dominant Gene ◽  
Avena Sterilis ◽  
Oat Crown Rust ◽  
Crown Rust Resistance ◽  
Resistance Spectrum ◽  
Dominant Genes

The inheritance of resistance to oat crown rust was studied in three accessions of Avena sterilis L. Accession CAV 4274 originated from Morocco, CAV 4540 from Algeria, and CAV 3695 from Tunisia. Seedling rust tests on F2 backcross families indicated the presence of two dominant genes for crown rust resistance in CAV 4274. One of these, a gene conditioning resistance to most races tested, was linked or allelic to gene Pc-38, and was designated gene Pc-62. The second gene conferred resistance only to one of the six races studied, and was not tested further. In CAV 4540, a single dominant gene, Pc-63 was possibly allelic with Pc-62 and linked or allelic to Pc-38. Genes Pc-62 and 63 are generally similar to Pc-38 in their resistance spectrum, but these three genes are differentiated by races CR 102, CR 103, and CR 107. A single dominant gene in CAV 3695 appeared to be Pc-50.

THE INHERITANCE OF LOOSE SMUT RESISTANCE.: I. THE INHERITANCE OF RESISTANCE IN FOUR BARLEY VARIETIES IMMUNE TO RACE 2 OF LOOSE SMUT

1962 ◽  
Vol 42 (1) ◽  
pp. 69-77 ◽  
Author(s):  
E. N. Larter ◽  
H. Enns
Keyword(s):  
Disease Resistance ◽  
Dominant Gene ◽  
The Other ◽  
Inheritance Of Resistance ◽  
Single Dominant Gene ◽  
Loose Smut ◽  
Race 2 ◽  
Or Genes ◽  
Dominant Genes

Four barley varieties, each immune to a Valki-attacking culture of loose smut (designated as race 2), were studied with respect to the inheritance of their resistance. Jet (C.I. 967) and Nigrinudum (C.I. 2222) were each found to possess two independent dominant genes determining resistance. Steudelli (C.I. 2266) proved to be immune to race 2 through the action of a single dominant gene, while resistance of Hillsa (C.I. 1604) was found to be conditioned by two complementary dominant genes. The absence of susceptible F3 families in crosses between Jet, Nigrinudum, and Steudelli indicated that these three varieties have in common a gene or genes for resistance to the race of smut used. The two complementary genes for resistance in Hillsa proved to be distinct from those of the other three varieties under study.The use of genetic analyses of disease resistance based upon classification of F3 families of the backcross to the resistant source is described and the merits of such a method are discussed.

scholarly journals The determination of the resistance inheritance against common bunt in wheat and half-diallel hybrids

2019 ◽  
Vol 55 (No. 4) ◽  
pp. 254-260
Author(s):  
Gülçin Akgören Palabiyik ◽  
İsmail Poyraz ◽  
Ahmet Umay
Keyword(s):  
Disease Resistance ◽  
Bread Wheat ◽  
Resistance Genes ◽  
Common Bunt ◽  
Wheat Varieties ◽  
Complete Dominance ◽  
Selection For ◽  
Half Diallel ◽  
Dominant Genes

This study was conducted to determine the inheritance of common bunt resistance in twelve bread wheat varieties and their half-diallel hybrids in Turkey. The disease ratings were performed on the F2 generations of the hybrids in field conditions. The obtained data were analysed by the χ2 test to determine the effective gene numbers and inheritance type in the disease resistance. In addition, the data were evaluated according to the Jinks-Hayman diallel analyses. In conclusion, it was found that of the twelve wheat parents, four contained three resistance genes and four of them contain two resistance genes. The dominant genes were prominent in the population and complete dominance was present. Therefore, the selection for disease resistance should be delayed until the following generations.

The inheritance of resistance to Puccinia coronata and of floret characters in Avena sterilis

1983 ◽  
Vol 25 (4) ◽  
pp. 329-335 ◽  
Author(s):  
L. S. L. Wong ◽  
R. I. H. McKenzie ◽  
D. E. Harder ◽  
J. W. Martens
Keyword(s):  
Rust Resistance ◽  
Dominant Gene ◽  
Crown Rust ◽  
Puccinia Coronata ◽  
Inheritance Of Resistance ◽  
Avena Sterilis ◽  
Field Isolates ◽  
Crown Rust Resistance ◽  
Dominant Genes

The inheritance of resistance to Puccinia coronata, awn development, lemma pubescence, and lemma color were studied in the Avena sterilis accessions CAV 4248, CAV 4656, and CAV 4904. Three independent, partially dominant genes (Pc-64, Pc-65, Pc-66) in CAV 4248, one partially dominant gene (Pc-67) in CAV 4656, and a dominant gene (Pc-68) in CAV 4904 were identified which conferred resistance to P. coronata. Genes Pc-64, Pc-65, Pc-66, Pc-67, and Pc-68 conferred resistance to 13, 8, 6, 12, and 14 races, respectively, of the 14 races of P. coronata tested. Gene Pc-68 conferred resistance to all field isolates of P. coronata collected in Canada in 1981 and was found to be closely linked or allelic to gene Pc-46. Awns and lemma pubescence were inherited monogenically in crosses with all three CAV accessions. Grey lemma color was controlled by one gene in CAV 4248 and by two genes in CAV 4656. Brown lemma color was controlled by one gene, which was closely linked or pleiotropic with the gene for lemma pubescence in CAV 4904. There was no association between crown rust resistance and the three floret characters studied.

Vernalization responses in narrow-leafed lupin (Lupinus angustifolius) genotypes

1995 ◽  
Vol 46 (5) ◽  
pp. 1011 ◽  
Author(s):  
KF Landers
Keyword(s):  
Genetic Basis ◽  
Major Gene ◽  
Mutant Gene ◽  
Major Effect ◽  
Lupinus Angustifolius ◽  
Vernalization Response ◽  
Essential Requirement ◽  
Breeding Lines ◽  
Sowing Dates ◽  
Absolute Requirement

Three experiments were conducted to characterize vernalization response in 13 diverse narrowleafed lupin (Lupinus angustifolius) genotypes, and to identify the genetic basis of differences in vernalization response. The aim was to better understand how flowering time may be manipulated in lupin breeding. The genotypes consisted of breeding lines with parents of wild origin, plus selected commercial varieties. Treatments included response to different periods of vernalization and response to different sowing dates. Most of the genotypes required vernalization for flowering. There were three types of response to vernalization observed; an absolute requirement, a reduced response, in which vernalization did not appear to be essential for flowering, and no response in lines carrying the natural mutant gene Ku (Gladstones and Hill 1969). In genotypes with an absolute requirement for vernalization, the period of vernalization at 5�C required to ensure flowering varied between 2 and 4 weeks, and flowering was hastened by increasing periods of vernalization. When vernalization was marginally inadequate, abnormal inflorescences formed. An apparent thermosensitive response, in which vernalization hastened flowering but did not appear to be essential, occurred in cv. Wandoo, which carries the gene �efl�. This response could also possibly be explained not by the lack of an essential requirement for vernalization, but by an ability of the cultivar to respond to vernalization at fairly high temperatures, around 16�C. Crossing studies identified a major gene the same as or allelic to �efl� in one genotype, but no other single genes with major effect on vernalization response were detected in genotypes of wild origin.

Seed coat specific weight in Lupinus angustifolius: influence of genotype and environment and relationship with seed coat proportion

2004 ◽  
Vol 55 (11) ◽  
pp. 1189 ◽  
Author(s):  
M. Mera ◽  
R. Jerez ◽  
H. Miranda ◽  
J. L. Rouanet
Keyword(s):  
Seed Coat ◽  
Seed Weight ◽  
Mass Density ◽  
Selection Criterion ◽  
Specific Weight ◽  
Equal Mass ◽  
Lupinus Angustifolius ◽  
Broad Sense ◽  
Broad Sense Heritability ◽  
Selection For

Abstract. The relatively high seed coat proportion of the narrow-leafed lupin reduces its economic value. This character has been shown to be affected by seed weight, and this limits the use of seed coat proportion as a selection criterion. We examined the variation for seed coat specific weight, a potential alternative selection criterion, and tested its relationship with seed coat proportion and seed weight. Seeds were sampled from mainstem pods of 14 winter-sown genotypes of Lupinus angustifolius L. grown at 4 southern Chile sites over 2 years. Seed coat specific weight had an overall mean of 30.1 mg/cm2. Highly significant genotypic effects were found (range 28.9–32.1 mg/cm2). The ranges for sites and years were 29.1–31.1 and 28.9–31.2 mg/cm2, respectively. Genotypes interacted significantly with years, but not with sites. Broad-sense heritability was 0.59, a value that predicts a good response to selection for this character. Seed coat specific weight was weakly correlated (rph = 0.11*) with seed coat proportion, and was not associated with mean seed weight. Seed coat proportion was negatively correlated with mean seed weight (rph = –0.75***) and had high broad-sense heritability (0.95). The correlation between seed coat specific weight and a theoretical seed coat thickness, calculated under the assumptions of equal mass density of seed coat, cotyledons, and embryo, and a spherical-shaped seed, was r = 0.14*. Phenotypic and genotypic correlations between seed coat specific weight and number of seeds per pod were 0.41 and 0.84, respectively. Our results indicate that selection for low seed coat proportion will lead to larger seeded genotypes, but will not reduce seed coat specific weight. Selection for low seed coat proportion after crosses would presumably be effective in reducing seedcoat specific weight if all segregating materials were uniformly large seeded, but that scenario is unrealistic. The evidence presented here suggests that selection for low seed coat specific weight (or measures correlated with it) in segregating populations will be necessary in order to increase the proportion of higher value kernels in seeds and to improve the economic yield of lupins.

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