RESUMEN
Switchgrass (Panicum virgatum L.) is a native perennial grass species with great potential for bioenergy and forage. However, knowledge about its genetics and biology related to breeding is still in its infancy. Studying the diversity of switchgrass germplasm will shed light on variability, response to environmental conditions, adaptability, breeding, etc. Thirty-six switchgrass accessions/cultivars were used to study the ecotypic and genotypic effects on regrowth, heading date, and vegetative growth period. The R-360 honeycomb design was used for planting these accessions in 2007. Data on regrowth and heading dates were recorded in 2008, 2010, and 2011. Vegetative growth period was calculated by subtracting the regrowth date from the heading date. It was found that the lowland started regrowing earlier (77 ± 0.4 days of the year, DOY) than the upland ecotype (82 ± 0.3 DOY). The upland had earlier heading date (160 ± 0.4 DOY) than the lowland ecotype (173 ± 0.5 DOY). Vegetative growth period was about 18 days longer in the lowland (89 ± 0.6 days) than the upland ecotype (71 ± 0.4 days). For switchgrass (i.e., all accessions), biomass yield was related positively to growth period and heading date; however, biomass was only weakly related to regrowth. Therefore, when targeting biomass in the breeding program, growth period may be a quick and reliable reference in both ecotypes to quickly estimate biomass potential while regrowth and heading date may be better used as a parameter for accessions within an ecotype.
RESUMEN
Allotetraploid white clover (Trifolium repens L.), a cool-season perennial legume used extensively as forage for livestock, is an important target for marker-assisted breeding. A genetic linkage map of white clover was constructed using simple sequence repeat (SSR) markers based on sequences from several Trifolieae species, including white clover, red clover (T. pratense L.), Medicago truncatula (Gaertn.) and soybean (Glycine max L.). An F(1) population consisting of 179 individuals, from a cross between two highly heterozygous genotypes, GA43 and Southern Regional Virus Resistant, was used for genetic mapping. A total of 1,571 SSR markers were screened for amplification and polymorphism using DNA from two parents and 14 F(1)s of the mapping population. The map consists of 415 loci amplified from 343 SSR primer pairs, including 83 from white clover, 181 from red clover, 77 from M. truncatula, and two from soybean. Linkage groups for all eight homoeologous chromosome pairs of allotetraploid white clover were detected. Map length was estimated at 1,877 cM with 87% genome coverage. Map density was approximately 5 cM per locus. Segregation distortion was detected in six segments of the genome (homoeologous groups A1, A2, B1, B2, C1, and D1). A comparison of map locations of markers originating from white clover, red clover, and alfalfa (M. sativa L.) revealed putative macro-colinearity between the three Trifolieae species. This map can be used to link quantitative trait loci with SSR markers, and accelerate the improvement of white clover by marker-assisted selection and breeding.
