Effects of reforestation methods on genetic diversity of lodgepole pine: an assessment using microsatellite and randomly amplified polymorphic DNA markers

Citation
Br. Thomas et al., Effects of reforestation methods on genetic diversity of lodgepole pine: an assessment using microsatellite and randomly amplified polymorphic DNA markers, THEOR A GEN, 98(5), 1999, pp. 793-801
Citations number
68
Categorie Soggetti
Plant Sciences","Animal & Plant Sciences
Journal title
THEORETICAL AND APPLIED GENETICS
ISSN journal
00405752 → ACNP
Volume
98
Issue
5
Year of publication
1999
Pages
793 - 801
Database
ISI
SICI code
0040-5752(199904)98:5<793:EORMOG>2.0.ZU;2-P
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 D NA (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 w ere much higher for SSRs than for RAPDs. Expected heterozygosity ranged fro m 0.39 to 0.47 based on RAPDs and from 0.67 to 0.77 based on SSRs. The numb er 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 numb er of alleles at a locus. Both marker types showed that over 94% of the var iation was contained within the populations and that the naturally regenera ted stands sampled had lower (not significant) expected heterozygosity than the planted or unharvested stands. The group of seedlings (assessed by RAP Ds only) had expected heterozygosity and allele frequencies similar to thos e of the unharvested stands. Genetic distance measures were higher than obt ained previously in the species using isozyme markers. There was no correla tion between the two marker types for pair-wise genetic distances based on populations analyzed by both methods. Pair-wise genetic distance measures a nd an ordination of allele frequencies for both marker types showed little effect of geographic location or stand type on genetic similarity.