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Seed banking has been the single most significant reaction of the research community to the alarming rates of plant genetic erosion occurring in the wild. One enduring challenge for a wiser utilization of the resources enclosed in seed banks, however, has been the estimation of their genetic potentials for agriculture's benefit. Key to detecting in landraces and/or wild relatives of modern crops any allelic variant lost during domestication and crop improvement is the use of molecular information to determine structure, evolution, and function of the genes harbouring these alleles. This paper reviews some of the theoretical and statistical issues surrounding the use of molecular population genetics tools for the detection of agronomical valuable alleles in seed banks. Emphasis is made on the technical limitations imposed by seed banking that may lessen the success of integrated and multi-disciplinary molecular approaches. The influence that population stratification and linkage disequilibrium exert on specific experimental designs for a better understanding of the evolutionary history of potential agronomic-related genes is also examined.

Moderate seed dormancy is desirable in barley (Hordeum vulgare L.). It is difficult for breeders to manipulate seed dormancy in practical breeding programs because of complex inheritance and large environmental effects. Quantitative trait locus (QTL) mapping opens a way for breeders to manipulate quantitative trait genes. A seed dormancy QTL, SD2, was mapped previously in an 8-cM interval near the chromosome 7 (5H) L telomere from a cross of 'Steptoe' (dormant)/'Morex' (non-dormant) by the North American Barley Genome Project using an interval mapping method and a relatively low-resolution genetic map. SD2 has a moderate dormancy effect, which makes it a promising candidate gene for moderate seed dormancy in barley cultivar development. The fine mapping of SD2 is required for efficient manipulation of SD2 in breeding and would facilitate the study of dormancy in barley. Ten different Morex isolines were generated, including regenerated Morex, of which nine lines had duplicates. The isolines together with Steptoe and Morex were grown in growth room and field environments for 2 years (2000 and 2001). In the growth room, relatively low growing temperatures (25 degrees C day/15 degrees C night) were employed to promote seed dormancy development. Seed germination percentage, determined at different post-harvest after-ripening periods, was used to measure seed dormancy. Fine mapping using the substitution mapping method based on differences among isolines resolved the SD2 QTL into an 0.8-cM interval between molecular markers MWG851D and MWG851B near the chromosome 7 (5H) L telomere. Relatively low temperatures (< or =25 degrees C) during seed development promoted the expression of the SD2 dormancy QTL. The chromosome region above the MWG851D-MWG851B interval might play a role in reducing barley seed dormancy during after-ripening.

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