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Previous studies have shown that there is considerable population structure in cultivated barley (Hordeum vulgare Lo), with the strongest structure corresponding to differences in row number and growth habit. U.S. barley breeding programs include six-row and two-row types and winter and spring types in all combinations. To facilitate mapping of complex traits in breeding germplasm, 1816 barley lines from 10 U.S. breeding programs were scored with 1536 single nucleotide polymorphism (SNP) genotyping assays. The number of SNPs segregating within breeding programs varied from 854 to 1398. Model-based analysis of population structure showed the expected clustering by row type and growth habit; however, there was additional structure, some of which corresponded to the breeding programs. The model that fit the data best had seven populations: three two-row spring, two six-row spring, and two six-row winter. Average linkage disequilibrium (LD) within populations decayed over a distance of 20 to 30 cM, but some populations showed long-range LD suggestive of admixture. Genetic distance (allele-sharing) between populations varied from 0.11 (six-row spring vs. six-row spring) to 0.45 (two-row spring vs. six-row spring). Analyses of pairwise LD revealed that the phase of allelic associations was not well correlated between populations, particularly when their allele-sharing distance was >0.2. These results suggest that pooling divergent barley populations for purposes of association mapping may be inadvisable. doi: 10.2135/cropsci2009.04.0198

Restoration of native plant communities requires adapted germplasm; thus, information is needed to guide native seed collection and production. Analysis of genetic variation has potential to provide insight into diversity and relatedness of natural populations. Our objectives were to examine genetic diversity of native species in Minnesota to discover if variation is related to biomes or distance, and possibly to develop seed collection zones. Our study included prairie cordgrass (Spartina pectinata), purple prairie clover (Dalea purpurea), and spotted joe-pye weed (Eupatorium maculatum). Using amplified fragment length polymorphisms, we analyzed 100 samples from eight populations for prairie cordgrass, 152 samples from nine populations for purple prairie clover, and 127 samples from 10 populations for spotted joe-pye weed. We found moderate to high levels of genetic diversity within each species. Small populations were not necessarily lower in diversity than larger ones. Analysis of molecular variance results indicate clear population differentiation. However, rather than displaying geographic or ecological associations, the variation had discontinuous patterns. Therefore, we were not able to develop unambiguous recommendations for seed collection. We discuss the applicability of molecular markers in detecting adaptive potential.

Kernel color and grain protein concentration (GPC) are two of the most important attributes of barley (Hordeum vulgate L.) grain intended for use in malting and brewing. Grain with protein levels that are too low or high or that have dark kernel color, which may result from the disease complex of kernel discoloration (KD), is unacceptable for the malting and brewing industries. The purpose of this study was to use molecular markers to map quantitative trait loci (QTLs) for KD and GPC in two recombinant inbred line (RIL) populations. One population was created by means of the high GPC and KD resistant cultivar Chevron. The other population was created from a KD resistant cultivar MNBrite that was derived from Chevron through eight generations of crossing and selection for bright kernels. The traits KD and GPC were evaluated in four and three environments, respectively, using the Chevron population and six environments using the MNBrite population. GPC and KD score were negatively correlated in both populations. A revised genetic map for the Chevron/M69 population, with an additional 45 simple sequence repeat (SSR) markers, was used to identify nine QTLs associated with KD on chromosomes 1(7H), 2(2H), 4(4H), 6(6H), and 7(5H), including two major QTLs on chromosome 6(6H). A single QTL for GPC identified in the Chevron mapping population, accounting for over 55% of the phenotypic variation, was located on chromosome 6(6H) and was coincident with one of the two major QTLs for KD. In this region, the Chevron allele increased GPC and decreased KD score. In the MNBrite mapping population, the same region of chromosome 6(6H) was mapped with SSR markers, and QTL analysis verified that this region was associated with both KD and GPC, indicating that MNBrite inherited this region of chromosome 6(6H) from Chevron. The results of this study suggest that if GPC and KD are controlled by tightly linked genes, then it should be possible to use SSR markers to identify recombinants in this region of chromosome 6(6H) and break the linkage to allow selection for KD resistance without high GPC. Alternatively, if GPC and KD are conditioned by the same gene, then it should he possible to select for KID resistance from Chevron by means of SSR markers and to use phenotypic selection to introgress other genes to reduce GPC to acceptable levels., KERNEL COLOR AND GPC are two of the most important selection criteria for determining whether barley grain is of sufficient quality for malting and brewing. Kernel color is negatively affected [...]