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Call number: LD2668 .T4 1952 A4 / Master of Science

Making quality and winterhardiness in barley are "ultimate" phenotypes composed of component, quantitatively inherited traits. A 69-point genome map of the seven chromosomes of barley was used, in conjunction with multi-environment phenotypes for grain yield and malting quality, to determine the chromosome locations of quantitative trait loci (QTLs). A combined analysis of the two environments identified QTLs that were both common and unique to each environment. Dispersed QTLs with positive relationships provide ready targets for marker-assisted selection. Overlapping QTLs for agronomic and making quality QTLs with favorable alleles contributed by alternate parents will require further, higher resolution mapping to determine if negative relationships are due to linkage or pleiotropy. There is preliminary evidence for orthologous agronomic trait and malting QTLs in barley. This QTL analysis will hopefully assist in the rapid development of winter making varieties that will maximize the profitability of Oregon barley production. / Graduation date: 1994

Graduation date: 1991

Barley grain is one of the main sources of feed for ruminants in Canada. Although barley varieties may have similar chemical composition, they exhibit different rumen degradation characteristics and nutrient availabilities. These biological differences may be related to structural chemical make-up or structural features among the varieties. The objectives of this study were to use the in situ technique and two Mid-IR Spectroscopy techniques, Diffuse Reflectance Fourier Transform IR Spectroscopy (DRIFT) and Synchrotron-based Fourier Transform IR Microspectroscopy (SFTIRM) to determine ruminal nutrient availabilities and inherent structural features in the hull, seed and endosperm of six barley varieties (AC Metcalfe, McLeod, CDC Dolly, CDC Helgason, CDC Trey, and CDC Cowboy) and to study the relationships between structural characteristics, mean and median particle size and nutrient availability. The nylon bag technique was used to incubate coarsely dry-rolled barley samples for 0, 2, 4, 8, 12, 24 and 48 h in the rumen of three mature Holstein dry dairy cows, which were ruminally cannulated. The rumen degradation kinetics of dry matter (DM), crude protein (CP) and starch were determined using first order degradation kinetics equations. Results indicated that there were significant differences in the mean and median particle size, degradation kinetics of each individual nutrient (DM, CP, and starch) among the six barley varieties. CDC Helgason showed the lowest degradation rate and extent of all nutrients (DM, CP, and starch) among the six barley varieties with larger particle size. Compared with other five varieties, CDC Helgason may be more suitable for ruminants feeding because of the lowest degradation rate and extent. The results also revealed a strong correlation between median particle size and the rate and extent of rumen degradation.<p> The results also showed that both DRIFT and SFTIR techniques associated with uni- and two multi- variate analyses were capable to efficiently discriminate and classify the inherent molecular structural features among the different varieties of barleys. Uni-variate analyses were conducted using both the DRIFT spectroscopy (hull and whole seed sample) and SFTIR microspectroscopy (endosperm tissue). The results from hull samples showed significant differences in the peak area of aromatic lignin, cellulosic compound, and total carbohydrates (CHO), and the ratio of lignin to cellulosic compound among the six barley varieties. The results from whole seed samples showed significant difference in the peak area and height of Amide I, peak area of total CHO and structural CHO (cellulosic), and the ratio of Amide I to total CHO area, and the ratio of total CHO to structural CHO. Significant differences were also found in the SFTIR results from endosperm tissue. With two multivariate spectral analysis techniques: Agglomerative hierarchical cluster (AHCA) and Principal component analyses (PCA) applied on whole seed sample, the CDC Helgason was distinguished from AC Metcalfe, CDC Dolly, McLeod and CDC Cowboy in fingerprint (1800-800 cm-1) and CHO region (1185-800 cm-1), from AC Metcalfe, McLeod and CDC Cowboy in protein region (1715-1485 cm-1). Information from this study involving probing the seed internal structure of barley may provide a further insight as to why barley varieties exhibit different rumen degradations.