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3. Objectives and results of barley (Hordeum vulgare L.) breeding

The main objectives of barley breeding in Japan are as follows: early maturity, cold resistance including tolerance to deep snow, short strong culm, high-yielding ability, disease resistance (barley yellow mosaic, barley yellow dwarf, powdery mildew, scab, etc.) and improved grain quality.


1) Breeding for early maturity, cold resistance, short strong culm and high-yielding ability: In Japan barley is sown in autumn, except in Hokkaido. Barley is the second crop in a rotation with rice or summer upland crops. Consequently, the interval between the harvesting of barley and the transplanting or sowing of the succeeding crops is very short. Double cropping is not possible in the northern part of Japan. To prevent maturity falling in the rainy season, early June to late July, it is essential to breed cultivars that mature as early as possible.

In the case of 6-rowed hulled barley, tall and late maturing, normal types of barley used to be grown, especially in Kanto district. However, due to the increased application of chemical fertilizers, improvement in lodging resistance of barley cultivars has become necessary. In order to breed cultivars resistant to lodging, there are two breeding strategies: 1) reduction of culm length, and 2) increase of culm stiffness. In the first strategy, the uz gene has been used for reducing the culm length. Tall and late maturing, normal types have been replaced by the semi-dwarf "uzu" type of cultivars which are early maturing and short, but retain a high yielding potential. In the second strategy, the cultivar Haganemugi has been used as a gene source for increasing culm stiffness. Haganemugi has stronger culm as a result of a thicker culm wall and a larger culm diameter (Oda et al. 1966). This results in a higher resistance to culm breaking when compared with a representative "uzu" type, Sekitorisai 1 (
Table 2). Several cultivars have been developed from crosses involving Haganemugi.


2) Breeding for resistance to barley yellow mosaic virus (BaYMV): Barley yellow mosaic caused by BaYMV previously inflicted serious damage especially on two-rowed malting barley. Gene sources and virus strains have been identified, and effective resistant cultivars have been developed (Table 3).

In Japan, three virus strains, I, II and III, have been identified (Usugi et al. 1985; Kashiwazaki et al. 1989). Strain I shows the widest distribution in the country followed by strain II, and strain III now occurs in a limited small area in Ibaraki Prefecture (Usugi et al. 1985; Kashiwazaki et al. 1989).

Five resistance genes, Ym, Ym2, ym3, ym4 and Ym5(t), have been identified in Japan (
Table 3). The variety Mokusekko 3 has two resistant genes Ym and Ym5(t) (Makino, personal communication). Ym is an incompletely dominant gene and linked to the gene K conferring hooded lemma with a recombination value of 29.4% on chromosome 4 (Takahashi et al. 1970). The resistance reaction of Ym to BaYMV strains I, II and III is probably S (susceptible), R (resistant) and R, respectively (Makino, personal communication). Ym5(t) is also incompletely dominant gene and linked to the complex loci (Est1-Est2-Est4) for the esterase isozymes with the recombination values ranging from 1.26 to 5.01 % on chromosome 3 (Konishi et al. 1989). The resistance reaction of Ym5(t) to BaYMV strains I, II and III is R, R and S, respectively (Makino, personal communication).

The variety Mihorihadaka has the resistant gene
Ym2 which is incompletely dominant and linked to the gene n conferring naked caryopsis with a recombination value of 31.4% on chromosome 1 (Takahashi et al. 1970). The resistance reaction of Ym2 to BaYMV strains I, II and III is R, S and R, respectively (lida et al. 1992).

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