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29<br />

cytological checks of the aneuploid constitution of<br />

monosomic materials, another glasshouse generation of<br />

self-pollination and molecular checks of chromosome<br />

substitutions using SSR markers of DNA were done.<br />

The presence of chromosome substitutions was<br />

confirmed in the substitution lines Mironovskaya 808<br />

(Bezostaya 1 5A), Bezostaya 1 (Mironovskaya 808 5A),<br />

Mironovskaya 808 (Bezostaya 1 5B) and Bezostaya 1<br />

(Mironovskaya 808 5B). These lines were used in the<br />

study of the relationship between vernalization<br />

response under the presence of recessive genes vrn-1<br />

and frost resistance. (Pánková K., Milec Z.)<br />

Phase 7: Study of wheat rust populations,<br />

powdery mildew and common bunt<br />

During the 2<strong>00</strong>6 vegetation period 72 isolates of leaf<br />

rust from 23 localities were obtained and tested on<br />

NILs with Lr genes (Lr1, Lr2a, Lr2b, Lr2c, Lr3, Lr9,<br />

Lr11, Lr15, Lr17, Lr19, Lr21, Lr24, Lr26, Lr28, Lr37).<br />

No virulence was found on NILs possessing Lr9 and<br />

Lr19 and Lr24.<br />

Gene for % virulent Gene for % virulent<br />

resistance isolates resistance isolates<br />

Lr 1 12 Lr 15 70<br />

Lr 2a 15 Lr 17 66<br />

Lr 2b 25 Lr 19 0<br />

Lr 2c 70 Lr 21 91<br />

Lr 3 94 Lr 23 86<br />

Lr 9 0 Lr 24 0<br />

Lr 10 95 Lr 26 72<br />

Lr 11 92 Lr 28 12<br />

In a field test with an inoculated spreader the resistance<br />

of newly registered cultivars and advanced lines to<br />

stem rust, yellow rust and leaf rust was tested.The results<br />

were compared with greenhouse tests. Main attention<br />

was paid to leaf rust. Most accessions possessing genes for<br />

specific leaf rust resistance were susceptible in field tests.<br />

The cultivar Batis was susceptible to all tested leaf rust<br />

isolates in the greenhouse but resistant in the field.<br />

In the field trials reactions of 30 cultivars and advanced<br />

lines of winter wheat, 12 cultivars of winter triticale<br />

and 3 cultivars of winter barley were tested for resistance<br />

to common bunt. Seed was inoculated with<br />

a mixture of Tilletia tritici and T. laevis. A low disease<br />

level was observed in 11 winter wheat cultivars and<br />

lines. No bunt occurred on cvs. Magnifik, Tommi,<br />

Trintella and line SW 51136. Average bunt incidence<br />

below 5% was determined in cvs. Globus, Mikon and<br />

Stava. In cultivars Bill, Lars and Tarso average bunt in<br />

cidence did not exceed 10%. Of the tested triticale cv.<br />

Ticimo had 0.4% bunted ears, cv. Triamant 2%, other<br />

10 triticale cultivars had no bunt infection. On winter<br />

barley after inoculation common bunt was not<br />

observed.<br />

In the field experiments the resistance of newly<br />

registered cultivars and advanced lines to powdery<br />

mildew was tested but the occurrence of powdery<br />

mildew was very low in consequence of high temperatures<br />

in that year (2<strong>00</strong>3, mainly in June). During the<br />

vegetation period 20 isolates of powdery mildew were<br />

obtained and tested on differential varieties with different<br />

Pm genes (Pm1; Pm2; Pm3a; Pm3b; Pm3c; Pm4a;<br />

Pm4b; Pm5; Pm6; Pm8; Pm17; Pm2, 6; Pm2, 4b, 8;<br />

Pm3d; Pm7; Pm1, 2, 9).Tests of the resistance of wheat<br />

cultivars to Septoria tritici blotch on leaf segments were<br />

started. Resistance of the tested cultivars fluctuated<br />

with used isolates of the pathogen.The effectiveness of<br />

inductors of systemic acquired resistance to powdery<br />

mildew in wheat was examined. All used inductors<br />

except salicylic acid induced resistance to powdery<br />

mildew. (Hanzalová A., Barto‰ P., Dumalasová V.,<br />

Vûchet L.)<br />

Utilization of innovated methods and specific<br />

breeding materials to increase the effectiveness<br />

of production of new winter rapeseed cultivars<br />

(Project MZe âR 1G46<strong>06</strong>1)<br />

About 1 6<strong>00</strong> new doubled haploid (DH) regenerants<br />

from F1 initial materials for the breeding of line and<br />

hybrid cultivars were developed. Advanced DH lines<br />

were evaluated in location trials and they yielded 90.46<br />

–1<strong>00</strong>.09% in comparison with standard cultivars.<br />

Eleven reliable restorers of fertility (Rf) for CMS<br />

Ogu-INRA with improved <strong>00</strong> quality were selected.<br />

The method of DNA markers for fatty acid assessment<br />

showed a high correlation coefficient for linolic acid<br />

with the standard method of gas chromatography.<br />

DNA analysis of self-incompatible (SI) plants based on<br />

PCR RFLP was found to be reliable for the detection<br />

of SI genotypes. Three F1 hybrids of CMS Shaan 2A<br />

lines with cv. Californium were obtained by means of<br />

honeybees as pollinators in isolation cages.<br />

Calibration equations for a laboratory instrument<br />

Foss-NIRSystem 65<strong>00</strong> were developed for the assessment<br />

of oleic, linolic and linolenic acid content.<br />

Molecular SCAR marker for the detection of fertility<br />

restorers (Rf) for Ogu-INRA has been successfully<br />

verified.<br />

Based on field and laboratory testing several sets of<br />

breeding materials with different susceptibility to<br />

important pathogens were created and included in field<br />

trials.Ten advanced DH lines were included in location<br />

performance trials. (Kuãera V., Vyvadilová M.,<br />

Klíma M.)<br />

Utilization of a protoplast fusion technique<br />

in the breeding of important cultivated crops<br />

of the genera Brassica, Cucumis and Solanum<br />

(MZe âR QF4108)<br />

Haploid (H) and doubled haploid (DH) regenerants<br />

derived from 3 cultivars of B. juncea (Domo, Opaleska,<br />

RLM 619) and B. carinata genotype BC11 are cultured<br />

in vitro as a source of protoplasts. Interspecific chemical<br />

fusions were carried out between DH B. carinata x DH<br />

OP-1 B. napus and H B. carinata x H B. juncea cv.<br />

Domo. Division of protoplasts and shoot regeneration<br />

were achieved in all fusion combinations. Regenerants<br />

from fusions between mesophyll protoplasts of DH B.<br />

carinata and hypocotyl protoplasts of DH OP-1 B. napus<br />

are prepared for laboratory and greenhouse evaluation.<br />

Whole plants were also developed after the protoplast

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