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Annual Progress Report on Malting Barley Research March, 2002

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110<br />

resistance. Some of the lines show good resistance to the apparent new stripe rust<br />

virulence at Huancayo, Peru.<br />

We are focusing our winter malting barley efforts <strong>on</strong> genotypes that do not require<br />

vernalizati<strong>on</strong>. Results for our mapping lead us to hypothesize that in the development of<br />

88ab536 there was either a crossover event leading to the separati<strong>on</strong> of the genes that<br />

determine cold tolerance and vernalizati<strong>on</strong> <strong>on</strong> chromosome 7 (5H) or that an allelic<br />

architecture was created that leads to an epistatic down-regulati<strong>on</strong> of the vernalizati<strong>on</strong><br />

requirement. These hypotheses will be elaborated <strong>on</strong> in our proposal for c<strong>on</strong>tinued<br />

funding. The immediate practical implicati<strong>on</strong> is that most of our winter malting barley<br />

selecti<strong>on</strong>s can be spring-sown. This would offer a safety net to growers, in the event of<br />

extensive winter injury, and it could lead to the development of varieties with very broad<br />

adaptati<strong>on</strong>. The yield of some of the winter selecti<strong>on</strong>s under spring-sown c<strong>on</strong>diti<strong>on</strong>s is<br />

competitive (Table 7). We hypothesize that the agr<strong>on</strong>omic potential of these lines may<br />

be limited by the malting quality d<strong>on</strong>or (Morex, via 88Ab536). Accordingly, as will be<br />

elaborated <strong>on</strong> in our proposal for c<strong>on</strong>tinued funding, we propose to transfer winter<br />

hardiness QTL alleles to more recent Midwestern malting quality varieties and thus raise<br />

the bar of agr<strong>on</strong>omic performance. Quality samples of the spring-sown winter malting<br />

selecti<strong>on</strong>s were submitted, but data have not been received, so the c<strong>on</strong>sistency of quality<br />

expressi<strong>on</strong> across sowing dates is not known at this point.<br />

The malting quality of winter selecti<strong>on</strong>s grown under fall-sown c<strong>on</strong>diti<strong>on</strong>s at Pendlet<strong>on</strong>,<br />

Pullman, and Aberdeen is shown in Table 6. For comparative purposes, we include the<br />

malting data from analyses of the same sample by different labs. Of these selecti<strong>on</strong>s,<br />

STAB 7 is in accelerated seed increase in preparati<strong>on</strong> for Plant Scale testing; STAB 7 and<br />

STAB 47 are currently both in a sec<strong>on</strong>d year of the AMBA Pilot program; and STAB 113<br />

is in a sec<strong>on</strong>d year of first level testing in the AMBA Pilot program. KAB 47 and KAB<br />

51 drill strips were planted at Pendlet<strong>on</strong> and Aberdeen in Fall, 2001 in preparati<strong>on</strong> for<br />

submissi<strong>on</strong> to the AMBA Pilot program.<br />

A notable feature of many of the winter malting selecti<strong>on</strong>s is low grain protein, and this<br />

leads to lower than desired specs for other malt parameters. So, while much of the rest of<br />

the barley research community struggles with ways to lower grain protein, we are<br />

working <strong>on</strong> ways to increase it. In cooperati<strong>on</strong> with S. Petrie and K. Rhinhart<br />

(Pendlet<strong>on</strong>) we initiated a series of management trials in the fall of 2001. We are<br />

c<strong>on</strong>tinuing with expanded versi<strong>on</strong>s of these trials this year and after this seas<strong>on</strong>, we will<br />

be able to present a comprehensive data analysis and a management package. At this<br />

point, it appears that we will be able to manage nitrogen (via split fall/spring<br />

applicati<strong>on</strong>s) in order to achieve target levels of grain protein and enzymatic properties.<br />

However, the timing of the split applicati<strong>on</strong>s will be critical, and there may be specific<br />

requirements for specific genotypes.<br />

Winter 6-row: 2001-<strong>2002</strong> seas<strong>on</strong><br />

Germplasm development<br />

Crosses are made at Corvallis and lines advanced to homozygosity through doubled<br />

haploid producti<strong>on</strong>, and/or single seed descent. With the emphasis <strong>on</strong> facultative growth<br />

habit, we are using SSD. With SSD, molecular markers can be used to indirectly select

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