Field assessment of partial resistance to powdery mildew in spring barley

Summary Partial resistance to powdery mildew in spring barley was evaluated in three plot types: large isolation plots, in 1.4 m² plots in chessboard design with guard plots of spring wheat and in single rows. Percentage leaf area covered by powdery mildew was scored four to six times during the season and partial resistance was characterized by the area under the disease progress curve. Varietal differences were revealed in al three plot designs, differences between the most resistant and susceptible genotypes being of a factor five. Differences between varieties decreased with decreasing plot size. The relationship between single scores of amount of powdery mildew on the upper four leaves and the area under the disease progress curve was high in all plot designs during the first two to three weeks after heading, allowing selection for the trait by one or two scorings. Differential ranking of varieties between different plot designs was observed, and is assumed to be due to increasing plot interference with reduced plot size and reduced distance between plots. A reliable selection for partial resistance could be made in large isolation plots and in 1.4 m² plots, but hardly in single rows.     

A novel resistance against powdery mildew found in winter barley cultivars

Barley powdery mildew caused by Blumeria graminis f. sp. hordei can be effectively controlled using genetic resistance. Moreover, specific resistances are also important for characterizing cultivars and verifying their origin, purity and authenticity. Winter barley is distinguished by several specific resistances, which are usually absent in spring barley. Besides responses caused by known genes, many cultivars showed a response suggesting the presence of an unknown resistance. Therefore, the aim of this research was firstly, to test winter barley cultivars, suspected to carry an unknown resistance gene, using a large collection of pathogen isolates for their expression of this specific response and to characterise the corresponding resistance. A set of 16 winter barley accessions originating from four gene banks was studied where each accession was represented by five single plant progenies. For resistance tests, 56 isolates of the pathogen were used. A new resistance with a proposed designation of Lu was found in all 16 selected accessions. Apart from Lu, eight well‐known Ml genes (a6, a8, a12, g, h, Lo, ra and Ru2) were postulated. Two accessions of cv. 'Borwina' originating from different gene banks were found to differ in their set of resistance genes.     

Identification of growth stage dependent expression of partial resistance of barley to powdery mildew

Summary Genotypic differences for growth stage dependent expression of partial resistance to barley powdery mildew have been identified on the basis of two components of resistance in the glasshouse and the pattern of epidemic development in the field.Differences for infection frequency and proportion of sporulating colonies were highly significant between the 16 genotypes investigated at four stages of plant development in the glasshouse. Both resistance components were significantly correlated mutually (r=0.73 to 0.86) and with the infection level on leaves developed at comparable growth stages in the field (r=0.52 to 0.73). The infection level of seedlings in the glasshouse was significantly correlated with the infection level of the leaves of the first until the third node in the field (r=0.70 to 0.73). Adult plant resistance was predominantly expressed at the uppermost leaf. A clear genotype × growth stage interaction was apparent for infection level; some genotypes showed partial resistance predominantly at the seedling stage and others predominantly at the adult plant stage.Abbreviations IF Infection Frequency, number of colonies per cm² leaf area, glasshouse experiment - IL Infection Level, number of colonies per cm² leaf area, field experiment - PSC Proportion Sporulating Colonies from total number of colonies, glasshouse experiment     

Sources of resistance to mildew and stripe rust in breeding spring barley

From 1960 onwards the Cereal Section of the Foundation for Agricultural Plant Breeding has paid much attention to seeking sources of resistance against yellow rust and mildew in barley.So far no variety has been found with a complete resistance to yellow rust. A number of varieties with at most a very slight degree of attack are mentioned in the tables.Mildew resistance in barley is discussed on the basis of German and Swedish data on the physiological specialization on barley.     

Identification of QTLs for powdery mildew and scald resistance in barley

A population of 103 recombinant inbred lines (RILs, F₉-derived lines) developed from the two-row spring barley cross L94 × ‘Vada’ was evaluated under field conditions for resistance against powdery mildew (Blumeria graminis f.sp. hordei) and scald (Rhynchosporium secalis). Apart from the major resistance gene mlo on chromosome 4 (4H), three QTLs (Rbgq1, Rbgq2 and Rbgq3) for resistance against powdery mildew were detected on chromosomes 2 (2H), 3 (3H), and 7 (5H), respectively. Rbgq1 and Rbgq2 have not been reported before, and did not map to a chromosome region where a major gene for powdery mildew had been reported. Four QTLs (Rrsq1, Rrsq2, Rrsq3 and Rrsq4) for resistance against scald were detected on chromosomes 3 (3H), 4 (4H) and 6 (6H). All four mapped to places where QTLs for scald resistance had been reported before in different populations.     

Assessment of partial resistance to powdery mildew in Chinese wheat varieties

Field trials in two cropping seasons and two locations in central China were conducted on 60 Chinese autumn‐sown wheat varieties to assess their partial resistance to powdery mildew. Mean levels of disease severity ranged from close to 0 to more than 90%. The method of inoculation and the location in which trials were conducted affected the relative performance of the varieties, but these effects were much smaller than the main effect of variety. The area under the disease progress curve was highly correlated with final disease severity, but both were poorly correlated with apparent infection rate. Disease severity was regressed against frequencies of virulence in the Blumeria graminis (syn. Erysiphe graminis) f sp. tritici populations in the trial plots. A vertical distance (D) from the mean mildew severity to the fitted line was calculated for each variety and was used to quantify partial resistance. Five of the 60 varieties, ‘Hx8541’, ‘E28547’, ‘Chuan1066’, ‘Zhe88pin6’ and ‘Lin5064’, consistently expressed relatively low levels of disease despite high frequencies of virulence in the pathogen and had consistently high D‐values. They may therefore have good levels of partial resistance.     

Mature plant resistance of barley to barley leaf rust,another type of resistance

Summary Seedling and flag leaves of three barley cultivars were simultaneously inoculated with urediospores of barley leaf rust, race 1-2-1, and incubated at the same greenhouse bench. The inoculated leaves were harvested before urediospore formation was initiated. The volume of a large number of colonies was estimated by measuring colony area and colony depth by embedding the colony containing leaf segments into paraffin for microtome cutting. The colony volume was considerably smaller in flag leaves than in seedling leaves even in the extremely susceptible cultivar. On average the difference was about tenfold.     

Spectrum of resistance conferred by ML-O powdery mildew resistance genes in barley

Summary Ten barley mutants and five Ethiopian barley lines representing 11 independently arisen powdery mildew resistance genes in the ml-o locus were tested at the seedling stage to cultures of the powdery mildew fungus from Europe, Israel, USA. Canada, and Japan. They were resistant with infection type 0/(4) in all tests. They were also resistant to field populations of the pathogen when scored in disease nurseries at more than 78 locations in 29 countries in Europe, the Near East, North and South America. New Zealand, and Japan. This indicates that the 11 genes confer the same, world-wide spectrum of powdery mildew resistance. They have no effect on several other barley diseases such as stripe rust and leaf rust.Part of the research reported here was carried out under IAEA Research Agreement No 1043 and Research Contract No 139-74-1 BIO DK with the European Atomic Energy Community.     

Further evidence of polygenic inheritance of partial resistance in barley to leaf rust,Puccinia hordei

Summary The latent period (LP) is a crucial component of partial resistance. Five cultivars, L94, Sultan (Su), Volla (Vl), Julia (Ju) and Vada (Va), representing the known range in partial resistance and LP were crossed in a diallel, and the F₁, F₂ and F₃ tested. The LP effectuated by the five cultivars is about 9, 10^1/2, 10^1/2, 13 and 15^1/2 days, respectively. The crosses Su×L94, Vl×L94 and Ju×L94 had an F₂ positively skewed. Their F₂ means were similar or only slightly larger than the F₁ means. The F₂ frequency distributions in the crosses Vl×Su, Ju×Su and Ju×Vl were normal or nearly so with F₁ and F₂ means similar to each other and to the mid-parent value. The crosses involving Va as a parent again showed a positive skewness but with F₂ means considerably larger than the F₁ moans.Most F₂'s ranged from the low parent to the high parent values without transgression. In the crosses Va×L94 (reported earlier) and Ju×L94 the parental values were not recovered among 216 and 154 F₂ plants, respectively. The cross Ju×Va showed transgression beyond the low parent, Ju.From these data it is concluded, assuming no linkage, that seven loci are involved. The + alleles (governing a longer LP) are thought to be distributed over the parents as follows: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGceaqabeaacaqGmb% GaaeyoaiaabsdacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabcca% caqGGaGaaeiiaiaab2cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiai% aabccacaqGGaGaaeiiaiaabccacaqGTaGaaeylaiaabccacaqGGaGa% aeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeylaiaab2caca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaa% b2cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaae% iiaiaabccacaqGTaGaaeylaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeiiaiaabccacaqGGaGaaeylaiaab2cacaqGGaGaaeiiaiaabc% cacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGTaGaaeyl% aiaabccaaeaacaqGtbGaaeyDaiaabccacaqGGaGaaeiiaiaabccaca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaa% bccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae% 4kaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqG% RaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaab2% cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeii% aiaabccacaqGTaGaaeylaiaabccacaqGGaGaaeiiaiaabccacaqGGa% GaaeiiaiaabccacaqGGaGaaeylaiaab2cacaqGGaGaaeiiaiaabcca% caqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGTaGaaeylaa% qaaiaabAfacaqGSbGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqGRaGaaeiiaiaabc% cacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqGRaGaaeii% aiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeylaiaab2cacaqGGa% GaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUca% caqGRaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiai% aab2cacaqGTaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGa% aeiiaiaabccacaqGTaGaaeylaiaabccacaqGGaGaaeiiaiaabccaca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaab2cacaqGTaaabaGaaeOs% aiaabwhacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGa% GaaeiiaiaabccacaqGGaGaae4kaiaabUcacaqGGaGaaeiiaiaabcca% caqGGaGaaeiiaiaabccacaqGGaGaae4kaiaabUcacaqGGaGaaeiiai% aabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaabccacaqGGaGa% aeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaabccaca% qGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGRaGaae4kaiaa% bccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaab2cacaqGTaGaae% iiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeylaiaab2caaeaacaqGwbGaaeyyaiaabccacaqGGaGaaeiiai% aabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcacaqGRaGa% aeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabUcaca% qGRaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaae4kaiaa% bUcacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaae% 4kaiaabUcacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqG% GaGaaeylaiaab2cacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabc% cacaqGGaGaae4kaiaabUcacaqGGaGaaeiiaiaabccacaqGGaGaaeii% aiaabccacaqGGaGaaeiiaiaabUcacaqGRaaaaaa!1BBA!\[\begin{gathered} {\text{L94 - - - - - - - - - - - - - - }} \hfill \\ {\text{Su + + + + + + - - - - - - - - }} \hfill \\ {\text{Vl + + + + - - + + - - - - - - }} \hfill \\ {\text{Ju + + + + + + + + + + - - - - }} \hfill \\ {\text{Va + + + + + + + + - - + + + + }} \hfill \\ \end{gathered} \]The genes are supposed to act additively (intermediate inheritance) with the exception of one locus (the 6th or 7th locus) which shows dominance for the shorter LP (for the-alleles). The effect of this locus on LP seems considerably larger than that of the other loci. There are indications of physiological barriers, which means that LP's shorter than the one of L94 or much longer than that of Va are not possible.The effect of + genes in genotypes governing LP's close to these barriers (with very few or very many + alleles respectively) is smaller than in genotypes governing intermediate LP's.     

Accumulating polygenes for partial resistance in barley to barley leaf rust,Puccinia hordei. II. Field evaluation

Summary Eight lines from the cross between Vada and Cebada Capa with long to very long latent periods and four barley cultivars representing the known range of partial resistance to barley leaf rust, caused by Puccinia hordei, were evaluated in the field for partial resistance and in the greenhouse for the latent period (LP) in the young flag leaf.Each of the 12 entries was sown (15-4-1983) on a plot of 1.0 m². There were four replicates. To reduce interplot interference the plots were separated from each other by 4.0 m of spring rye. The number of urediosori per tiller was evaluated at 27-6, 4-7, 12-7 and ten days after heading. The LP was measured on 10 to 15 plants per entry in 1982 and on 10 plants in 1983.The levels of partial resistance varied greatly. The difference in number of sori per tiller between the most susceptible cultivar, Akka, and the most resistant cultivar, Vada, was about 50 times. Between Akka and the most resistant line this was approximately 5000 times. The LP's varied similarly. Vada had a LP 64% longer than that of Akka, the LP of line 26-6-11 was 15% longer. The range of partial resistance has been extended more than twofold.The correlation coefficients between LP and the level of barley leaf rust, expressed in transformed scale units, varied from -0.99 for the first sampling date to -0.97 for the third sampling date. Sampling the same development stage, ten days after heading, did not improve the r-value (r=–0.98). The LP evaluated in the young flag leaf is shown to be a very reliable criterion for partial resistance in the barley-Puccinia hordei pathosystem.Earliness tends to be associated with susceptibility. The correlation of days to heading with LP was 0.63, and with the level of barley leaf rust in the field 0.64.     

Discovery,characterization and exploitation of Mlo powdery mildew resistance in barley

Summary Mlo resistance to barley powdery mildew is a relatively new kind of resistance. It was originally described in a powdery mildew resistant barley mutant in 1942 and has been mutagen-induced repeatedly since then. About 1970 it was also recognized in barley landraces collected in Ethiopia in the 1930s. It is unique in that 1) Mlo resistance does not conform to the gene-for-gene system; 2)mlo genes originating from different mutational events map as non-complementing recessive alleles in one locus; 3) all alleles confer the same phenotype, though with small quantitative differences; 4) it is effective against all isolates of the pathogen; and 5) the resistance is caused by rapid formation of large cell wall appositions at the encounter sites preventing penetration by the fungus. Powdery mildew isolates with elevated Mlo aggressiveness have been produced on barley in the laboratory, but have not been found in nature. Mlo resistance is considered very durable. The exploitation of Mlo resistance has been hampered by pleiotropic effects of themlo genes, vix. necrotic leaf spotting and reduced grain yield, but they have been overcome by recent breeding work. During the 1980s Mlo-resistant spring barley varieties have become cultivated extensively in several European countries, in 1990 on about 700,000 ha.     

Interplot interference and the assessment of barley cultivars for partial resistance to leaf rust,Puccinia hordei

Summary The barley cultivars Akka, highly susceptible, and Vada, partially resistant to barley leaf rust, Puccinia hordei, were evaluated for the amount of leaf rust in five experimental field plot situations over three successive years. The field plot situations were: A) plots well isolated from each other by distance and non-leaf rust contributing host plants; B) adjacent plots of 4×41/2 m (18 rows); C) adjacent plots of 4×11/2 m (6 rows); D) adjacent plots of 4×1/4 m (1 row); E) adjacent plots of only one plant (cultivar mixtures).The sporulating leaf area of each plot was measured from samples of 20 tillers taken at random from each plot. In each year the difference in sporulating area between Akka and Vada was large to very large in the absence of interplot interference in the isolated plots, ranging from 150 to 2100 times. In the adjacent plots the partial resistance of Vada was greatly underestimated, 5 to 16 times in the situation B, 14 to 30 times in C, and 75 to 130 times in D and E.Testing lines or cultivars in adjacent plots is the standard procedure in use in breeding programs and in tests of cultivars for their agricultural value. To avoid such under estimation the following procedure is suggested. A few cultivars representing the known range of partial resistance and whose level of partial resistance is well known are evaluated together with the lines and cultivars whose partial resistance has to be assessed. This is demonstrated with a number of cultivars of which resistance values are know from the recommended variety lists for England and Wales. Cultivars have been assessed in Wageningen over four years together with the check cultivars Akka, Sultan, Julia and Vada representing the range of partial resistance with values (on a 1 to 10 scale) of 1, 3–4, 7 and 8 respectively, based on isolated plots experiments.     

Partial resistance of barley to leaf rust,Puccinia hordei. V. Analysis of the components of partial resistance in eight barley cultivars

Summary Eight spring barley cultivars, respresenting the known range in partial or slow rusting resistance to leaf rust, Puccinia hordei, were investigated for their effects on the components of partial resistance; infection frequency, latent period, infectious period and spore production per uredosorus per day. Considerable variation was observed among the cultivars for each of the components. The cultivar effects on the components tend to be associated. Cultivar L94 for instance, shows the highest infection frequency, the shortest latent period and a long infectious period. Julia and Vada both have a low infection frequency, a long latent period and a low spore production per sorus per day. This association, though, is only a partial one.The total spore production per unit leaf area (the combined result of the four components) appeared highly correlated with the partial resistance in the field (r=0.85). Only a relatively small portion of the variation in partial resistance cannot be explained by the four components studied. Several other aspects, which might affect the rate of epidemic development, are discussed.Latent period, measuring the onset of the new spore production, estimated partial resistance as well as total spore production did (r=–0.85). In order to evaluate the partial resistance of barley genotypes in the greenhouse the latent period is preferred above total spore production as it is measured more easily, more accurately and sooner after inoculation.     

Molecular mapping of partial resistance to powdery mildew in winter wheat cultivar Folke

The Swedish winter wheat (Triticum aestivum L.) cultivar Folke has a long record of partial and race non-specific resistance to powdery mildew (caused by Blumeria graminis f. sp. tritici) in the field. The aim of the present study was to map the main genetic factors behind the partial resistance in Folke and identify molecular markers for use in marker-assisted selection. A population of 130 recombinant inbred lines was developed from a cross between Folke and the moderately susceptible spring wheat line T2038. The population was tested for powdery mildew resistance over two years at two locations in Norway and genotyped with DArT and SSR markers. Composite interval mapping detected a total of eight quantitative trait loci (QTL) for powdery mildew resistance; six with resistance from Folke on 2BS, 2DL, 5AL, 5BS and 6BS and two with resistance from T2038 on 5BS and 7AL. None of the loci with resistance from Folke mapped to chromosomal regions with known race-specific resistance genes, which confirmed the race non-specific nature of the resistance in this cultivar. The molecular markers linked to the reported QTL will be useful as a tool for selecting partial and potentially durable resistance to powdery mildew based on the resistance in Folke.     

Characterisation and origin of rust and powdery mildew resistance genes in VPM1 wheat

Summary The expression of rust resistances conferred by closely linked genes derived from VPM1 varied with environmental conditions and with genetic backgrounds. Under low light and low temperature conditions seedlings carrying Yr17 showed susceptible responses. Stem rust and leaf rust resistance genes Sr38 and Lr37 tended to confer more resistance at 17±2° C than at normal temperatures above > 20° C. These studies supported the hypothesis that Yr17, Lr37 and Sr38 were derived from Aegilops ventricosa, whereas Pm4b was probably derived from T. persicum. Studies on certain addition lines and parental stocks indicated that wheat cytoplasm may enhance the expression of Sr38.     

Level of partial resistance to leaf rust,Puccinia hordei,in West-European barley and how to select for it

Summary The partial resistance to leaf rust (Puccinia hordei) of 40 West-European spring barley cultivars was measured in plots isolated from one another to reduce inter plot interference. The leaf area affected by leaf rust was also measured in small plots of 0.5 m² adjacent to each other, and on individual plants. The latent period was measured in the seedling stage and the adult plant stage, the infection frequency in the seedling stage only. The cultivars varied widely for partial resistance, many cultivars carrying a considerable level. Both the small adjacent plots and the single plants showed a marked inter plot interference strongly reducing the difference between cultivars. H wever, the ranking order of the cultivars was hardly, if at all, affected. Both latent period and the infection frequency showed large differences between cultivars, the latent period in the adult plant stage being highly correlated (r=0.82) with partial resistance, infection frequency in the seedling stage only rather weakly (r=–0.33).Selection for partial resistance appeared very effective in all stages tested; the seedling, the single adult plant, and the small plot stage. Selection in the small plot stage was the most effective followed by selection in the seedling stage. Selection for partial resistance therefore appears very well possible at all stages of the selection program.     

Variation in partial resistance to barley leaf rust (Puccinia hordei) and agronomic characters of Ethiopian landrace lines

An inventory of 481 lines derived from 12 Ethiopian barley (Hordeum vulgare L.) landraces and the checks was made for partial resistance to Puccinia hordei under greenhouse and field conditions at Adet, Ambo and Sinana Agricultural Research Centers in 2003 and 2004 cropping seasons in Ethiopia. The experiments were laid out in a triple lattice design. Each plot consisted of two rows of 1–m long with spacing of 0.20 m between rows. The overall mean leaf rust epidemics varied from area under disease progress curve (AUDPC) of 86 to 1,835. The disease was as high as AUDPC 1,378 on the susceptible check L94. Highly significant variations were recorded between and within the landraces/lines in leaf rust incidence, severity, days to heading, plant height, thousand seed weight and yield. Similarly, the variations between and within barley groups from three altitude areas and three ear-types were significant. Landraces 1686, 3255, 3262 and 3783 had the least and landraces 219900, 3975 and 3980 had the highest leaf rust severity. Of the 481 lines tested, 413 (86%) had significantly lower disease than the susceptible check, but not than the partial resistant check Vada. In contrast, the yields were more for lines with less disease than for those with high. The frequency of resistant landraces/lines was more in altitude 2,301–2,500 m, and irregular and two rows ear-types than in lower altitude areas and six rows ear-type. Nevertheless, the correlation and regression analysis revealed the adverse effect of the disease in the yields of barley. The 413 lines with high infection types at seedling stage and lower AUDPC under field conditions possess partial resistance to leaf rust.     

Associations between three ml-o powdery mildew resistance genes and agronomic traits in barley

Summary A population of 198 chromosome-doubled haploid lines of spring barley was scored for segregation in locus ml-o (powdery mildew reaction) on chromosome 4 and in the linked loci s (rachilla hair length) and ddt (reaction to the insecticide DDT) on chromosome 7. They were also tested in a disease-free field trial for the agronomic traits: grain yield, thousand grain weight, lodging, and necrotic leaf spotting. The three mutagen-induced resistance genes ml-o5, ml-o6 (from Carlsberg II) and ml-10 (from Foma) showed no detectable differences with respect to effects on agronomic traits. They all conferred a four per cent reduction in grain yield caused mainly by lower thousand grain weight, and an increase in necrotic leaf spotting. The two original mutants of Carlsberg II had additional mutant genes affecting agronomic traits. Lines with gene S (long hair) had on average a three per cent higher thousand grain weight than those with s. The alleles in locus ddt showed no association with the agronomic traits. It is concluded i) that the associations between the three ml-o alleles and agronomic traits are caused by pleiotropy, ii) that ml-o resistant, high-yielding lines may be selected, and iii) that the association between gene s and thousand grain weight may be due to genetic linkage.Abbreviations DH-lines chromosome-doubled haploid lines     

Accumulating polygenes for partial resistance in barley to barley leaf rust,Puccinia hordei. I. Selection for increased latent periods

Summary The barley cultivar Cebaba Capa was crossed to the cultivar L94, which is assumed to carry no genes for increased latent periods, and Vada, which is assumed to carry five to six minor genes for a longer latent period (LP). In the F2 selection was carried out for short and long LP's in the young flag leaves to Puccinia hordei in both crosses. In the F3, F4 and F5 the selection for short as well as for long LP continued by selecting the extreme plants in the extreme lines, a typical pedigree selection approach.The LP's are given relative to those of L94, set at 100 and of Vada, set at 185. From the cross with L94 homogeneous lines were obtained with relative LP's of 100 and of 220. From the cross with Vada the extreme lines had LP's of 135 and around or even beyond 300.Cebaba Capa is thought to carry four to six minor genes with an average gene effect slightly larger than those of the five to six minor genes in Vada. From the four to six minor genes one or two may be identical to or closely linked with minor genes of Vada, the others appeared to be different. In the lines with LP's of close to 300 or even more the number of minor genes accumulated is thought to be in the order of eight or nine. These gene number estimates are based on independent assortment. If linkage occurs the number of genes involved may be larger.Because of the high correlation between LP in the young flag leaf and the partial resistance in the field the selected lines are assumed to have a partial resistance to barley leaf rust far beyond that of Vada, which represents almost the highest level of partial resistance in European cultivars.