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- Author or Editor: Brian M. Schwartz x
Bermudagrass (Cynodon spp.) is the foundation of the turfgrass industry in most tropical and warm-temperate regions. Development of bermudagrass as a turfgrass began in the early 1900s. Many of the cultivars commercially available today have been cooperatively released by the U.S. Department of Agriculture Agricultural Research Service (USDA-ARS) and the University of Georgia at the Coastal Plain Experiment Station in Tifton, GA.
Japanese-cedar [Cryptomeria japonica (L.f.) D. Don] represents an alternative to leyland cypress [×Cuprocyparis leylandii (A.B. Jacks. & Dallim.) Farjon] as an evergreen screen or specimen plant for landscapes. It performs well under a range of soil and environmental conditions but has been underused attributable, in part, to unsightly winter browning caused by photoinhibition. In previous studies, chance seedlings that did not exhibit winter browning were identified as tetraploids. The current study was conducted to induce polyploidy in japanese-cedar. Approximately 600 seedlings were sprayed with 150 μM oryzalin + 0.1% SilEnergy™ for 30 consecutive days under laboratory conditions. Two hundred thirty-seven seedlings with thickened and twisted leaves were selected, transplanted, and grown in a glasshouse for 120 days. Seedling ploidy levels were analyzed using flow cytometry 180 days after treatment (DAT), identifying 197 (83.1%) tetraploids, 22 (9.3%) cytochimeras, and 18 (7.6%) diploids. Morphology of induced tetraploids was similar to that previously described and provided a phenotypic marker during selection that was over 92% accurate. A random subset of 20 tetraploid individuals was analyzed 270 DAT and were found to contain only tetraploid cells in the leaves analyzed, confirming stability over this period. This study demonstrated the use of oryzalin for inducing tetraploids in japanese-cedar, which we predict will be effective in other gymnosperms.
The release of the bermudagrass (Cynodon spp.) triploid hybrid ‘Tifgreen’ revolutionized southeastern U.S. golf course greens. Off-types within this cultivar began to be identified soon after the initial plantings, and through the last 50 years, many of the best performing off-types have been released as new cultivars. Examination of some of the most popular somatic mutants with a new set of 47 simple sequence repeat (SSR) markers and 23 previously discovered genomic SSR markers identified five polymorphic fragments (as compared with ‘Tifgreen’) among three cultivars, TifEagle, MiniVerde, and Tifdwarf. Each polymorphism appears to be a slight increase/decrease in microsatellite repeat number and the polymorphic fragments are unique for each cultivar. Two polymorphic fragments were identified that were unique to ‘Tifdwarf’, one polymorphic fragment was unique to ‘TifEagle’, and two polymorphic fragments were unique to ‘MiniVerde’. Furthermore, three of the five polymorphic markers display an additional allele only in the shoot tissue but not in the root tissue of ‘TifEagle’ and ‘Tifdwarf’. This finding suggests that ‘TifEagle’ and ‘Tifdwarf’ are somatic chimeras. This set of SSR markers identifies repeatable polymorphic fragments among multiple ‘Tifgreen’-derived cultivars and gives insight into the nature of the mutations that exist within ‘Tifgreen’.
Thirty-one partial bermudagrass (Cynodon spp.) disease-resistance gene analogs (BRGA) were cloned and sequenced from diploid, triploid, tetraploid, and hexaploid bermudagrass using degenerate primers to target the nucleotide binding site (NBS) of the NBS–leucine-rich repeat (LRR) resistance gene family. Alignment of deduced amino acid sequences revealed that the conserved motifs of the NBS are present and all sequences have non-Drosophila melanogaster Toll and mammalian interleukin-1 receptor (TIR) motifs. Using a neighbor-joining algorithm, a dendrogram was created and nine groups of deduced amino acid sequences from bermudagrass could be identified from those sequences that span the NBS. Four BRGA markers and 15 bermudagrass expressed sequence tags (ESTs) with similarity to resistance genes or resistance gene analogs were placed on a bermudagrass genetic map. Multiple BRGA and EST markers mapped on T89 linkage groups 1a and 5a and clusters were seen on T89 19 and two linkage groups previously unidentified. In addition, three primers made from BRGA groups and ESTs with similarity to NBS-LRR resistance genes amplify NBS-LRR analogs in zoysiagrass (Zoysia japonica or Z. matrella) or seashore paspalum (Paspalum vaginatum). This gives evidence of conservation of NBS-LRR analogs among the subfamilies Chloridoideae and Panicoideae. Once disease resistance genes are identified, these BRGA and EST markers may be useful in marker-assisted selection for the improvement of disease resistance in bermudagrass.