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Annual Progress Report on Malting Barley Research March, 2007

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EARLY GENERATION LINES<br />

Forty F5 populati<strong>on</strong>s were grown at Crookst<strong>on</strong> and St. Paul. The populati<strong>on</strong>s were largely<br />

of two types, i.e., traditi<strong>on</strong>al elite by elite and elite by FHB resistant. Nine of the F5<br />

populati<strong>on</strong>s (elite by elite) al<strong>on</strong>g with eight populati<strong>on</strong>s segregating for resistance to net<br />

blotch or septoria were advanced through the F3 and F4 generati<strong>on</strong>s via single seed<br />

descent (SSD) in greenhouses in fall and winter 2005-2006. These populati<strong>on</strong>s were<br />

planted as F5 head rows in Crookst<strong>on</strong> or Stephen (net blotch) in the summer of 2006.<br />

Selecti<strong>on</strong> in these crosses was based <strong>on</strong> heading date, height, lodging, kernel plumpness,<br />

and spike characteristics. The Septoria and net blotch populati<strong>on</strong>s were planted in<br />

inoculated nurseries. We were unable to get good Septoria disease expressi<strong>on</strong> and<br />

therefore unable to select for resistance. These lines were screened for resistance to<br />

Septoria in the Fall greenhouse and resistant lines will be advanced to <strong>2007</strong> trials. Disease<br />

pressure at our net blotch nursery was light, so we also c<strong>on</strong>ducted greenhouse disease<br />

screening in the Fall. Twenty-four of the F5 populati<strong>on</strong>s (elite by FHB) were advanced to<br />

F3 in a fall 2005 greenhouse in Minnesota and then to the F4 as single plants in<br />

Christchurch, New Zealand. The New Zealand nursery allowed us to harvest enough seed<br />

from individual plants for replicated FHB nurseries in a timely manner for planting.<br />

Selecti<strong>on</strong> <strong>on</strong> FHB populati<strong>on</strong>s in the 2006 field seas<strong>on</strong> was based <strong>on</strong> FHB resistance,<br />

heading date, height, and lodging. Grain harvested from selected rows was analyzed for<br />

DON. In additi<strong>on</strong>, we plant a single row outside of the disease nursery for malting quality<br />

analysis in Madis<strong>on</strong>, WI. Heads from selected F5’s in 2006 were planted in single rows in<br />

a winter nursery (2006/<strong>2007</strong>) in Yuma, AZ to produce seed for 2006 PYTs. Based <strong>on</strong> 2006<br />

FHB, DON, and malting quality data and also phenotype in the Yuma nursery, about 200<br />

lines will be selected for entry to preliminary yield trials in <strong>2007</strong>.<br />

A total of 51 F2 populati<strong>on</strong>s were grown in the field at St. Paul and Crookst<strong>on</strong> in 2005. In<br />

additi<strong>on</strong>, we grew eight F2 populati<strong>on</strong>s in the summer greenhouse in c<strong>on</strong>es arranged in a<br />

96-well format to facilitate marker assisted selecti<strong>on</strong> (MAS). In these populati<strong>on</strong>s, we<br />

selected for markers linked to a QTL identified <strong>on</strong> chromosome 6(6) (Wingbermuehle et al.,<br />

2004) and markers linked to a QTL for resistance to Septoria speckled leaf blotch. Marker<br />

genotyping was d<strong>on</strong>e in collaborati<strong>on</strong> with Dr. Shiaoman Chao at the USDA Genotyping<br />

Lab in Fargo, ND.<br />

SCREENING FOR DISEASE RESISTANCE<br />

FHB<br />

Steady progress has been made in breeding for resistance to FHB. Funding through the<br />

US Wheat and <strong>Barley</strong> Scab Initiative and the Minnesota Small Grains Initiative have<br />

allowed us to sustain a major effort in disease resistance breeding and studies aimed to<br />

understand and exploit the genetics of disease resistance. Our FHB screening effort is<br />

c<strong>on</strong>ducted in collaborati<strong>on</strong> with Dr. Ruth Dill-Macky and Dr. Charla Hollingsworth. We are<br />

advancing resistant lines in our program tracing to different sources of resistance and<br />

c<strong>on</strong>tinue to make crosses with new sources of resistance as they are identified. We have<br />

been working with Dr. Brian Steffens<strong>on</strong> in selecting new sources of FHB resistance to<br />

introduce into the breeding program. Each year we have increased the number of entries<br />

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