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  • Gene conservation  (1)
  • Key words Stylosanthes  (1)
  • Springer  (2)
  • 1995-1999  (2)
  • 1990-1994
  • 1920-1924
  • 1905-1909
  • 1999  (2)
Collection
Publisher
  • Springer  (2)
Years
  • 1995-1999  (2)
  • 1990-1994
  • 1920-1924
  • 1905-1909
Year
  • 1999  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 99 (1999), S. 1179-1186 
    ISSN: 1432-2242
    Keywords: Key words Stylosanthes ; DNA markers ; Genetic relationships
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  Genetic relationships between 6 unclassified taxa and 24 known species of the genus Stylosanthes were investigated by RFLP and STS analyses. This allowed the diploid taxa used in this study to be classified into nine basal (genome) groups. Representative species in these groups included ’S. seabrana’/S. hamata (Group A), S. viscosa (Group B), S. humilis (Group C), S. macrocephala/S. bracteata (Group D), S. pilosa (Group E), S. leiocarpa (Group F), S. guianensis (Group G), S. tomentosa (Group H) and S. calcicola (Group I). Polyploid taxa used were grouped into five classes based on their putative genomic structures. These are AABB for S. scabra, S. aff. scabra, S. sericeiceps, S. aff. hamata and S. tuberculata; AACC for S. mexicana, S. subsericea, S. sundaica and S. sp.A; DDEE for S. capitata; AAFF for S. sympodialis; and AABBXX for S. erecta, with XX representing an unknown genome. Of the 6 unclassified taxa, three were diploids and 3 tetraploids. Of the 3 diploids, the genome of S. sp. was markedly distinct from those of all other diploids analysed in this study, with that of S. leiocarpa being the closest. The genome of S. sp.B was similar to that of S. humilis, with an average dissimilarity value of 15% between them. The genome of S. aff. viscosa was very similar to that of S. viscosa. Genetic variation between these 2 taxa was not larger than that within each of the 2 taxa. Of the 3 tetraploids, the genomic structure of S. sp.A was similar to those of S. mexicana, S. sundaica and S. subsericea, and the genomic structures of S. aff. scabra and S. aff. hamata were similar to those of S. scabra and S. sericeiceps.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2242
    Keywords: Key words Pinus contorta ; Silviculture ; Reforestation ; Gene conservation ; RAPD ; SSR ; DNA analyses
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  We examined the effects of different methods of forest regeneration on the genetic diversity of lodgepole pine (Pinus contorta var ‘latifolia’) using two different DNA-based molecular markers [randomly amplified polymorphic DNA (RAPDs) and microsatellites or simple sequence repeats (SSRs)]. Genetic diversity was estimated for 30 individuals in each of four populations for the following three stand types: (1) mature lodgepole pine (〉100 years); (2) 20- to 30-year-old harvested stands left for natural regeneration; (3) 20- to 30-year-old planted stands (4 stands of each type); and one group of 30 operationally produced seedlings. There was no significant effect of stand type on expected heterozygosity, although allelic richness and diversity were much higher for SSRs than for RAPDs. Expected heterozygosity ranged from 0.39 to 0.47 based on RAPDs and from 0.67 to 0.77 based on SSRs. The number of alleles per locus for SSRs ranged from 3 to 34 (mean 21.0), and there was a significant relationship between sequence repeat length and the number of alleles at a locus. Both marker types showed that over 94% of the variation was contained within the populations and that the naturally regenerated stands sampled had lower (not significant) expected heterozygosity than the planted or unharvested stands. The group of seedlings (assessed by RAPDs only) had expected heterozygosity and allele frequencies similar to those of the unharvested stands. Genetic distance measures were higher than obtained previously in the species using isozyme markers. There was no correlation between the two marker types for pair-wise genetic distances based on populations analyzed by both methods. Pair-wise genetic distance measures and an ordination of allele frequencies for both marker types showed little effect of geographic location or stand type on genetic similarity.
    Type of Medium: Electronic Resource
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