Using databases of previously published primers, we optimised six nuclear microsatellite markers for Prunus africana for the purposes of studying spatial genetic structure and gene flow. To assess variability, these and three previously transferred loci were screened in populations from Kenya and South Africa. Across both populations most loci were polymorphic, with the exception of a single locus which failed to amplify in the South African samples, exhibiting between 2 and 22 alleles and levels of expected heterozygosity (He) ranged from 0.059 to 0.932. Departures from Hardy–Weinberg equilibrium were detected for all loci but not for all populations. The estimated null allele frequency was very low to moderate and no evidence for linkage ...
Premise of the study: Multiplexes of nuclear microsatellite primers were developed to investigate po...
We developed eleven microsatellite markers for Hymenaea courbaril for the purposes of studying spati...
<p>Haplotype (cpSSR) (3a) and allelic (nSSR) (3b) richness are determined for 32 populations, after ...
<p>The 32 populations, represented by 30 minute grid cells, are grouped by Nei’s distance, based on ...
AbstractListed as vulnerable under Appendix II of CITES, populations of the commercially valuable Af...
Conservation priorities for Prunus africana, a tree species found across Afromontane regions, which ...
Studying fine-scale spatial genetic patterns across life stages is a powerful approach to identify e...
A total of 145 microsatellite primer pairs from Prunus DNA sequences were studied for transferabilit...
The utility of microsatellite markers to characterize the genetic diversity of a polyploid species w...
• Premise of the study: Microsatellites were designed and characterized in the African timber forest...
While the genetic structure of many tree species in temperate, American and Asian regions is largely...
Premise of the study: Multiplexes of nuclear microsatellite primers were developed to investigate po...
Premise of the study: Microsatellites were developed in the vulnerable African rainforest tree Afzel...
Refugia are expected to preserve genetic variation of relict taxa, especially in polyploids, because...
Premise Afzelia africana (Fabaceae) is a valuable, internationally vulnerable tree species in tropic...
Premise of the study: Multiplexes of nuclear microsatellite primers were developed to investigate po...
We developed eleven microsatellite markers for Hymenaea courbaril for the purposes of studying spati...
<p>Haplotype (cpSSR) (3a) and allelic (nSSR) (3b) richness are determined for 32 populations, after ...
<p>The 32 populations, represented by 30 minute grid cells, are grouped by Nei’s distance, based on ...
AbstractListed as vulnerable under Appendix II of CITES, populations of the commercially valuable Af...
Conservation priorities for Prunus africana, a tree species found across Afromontane regions, which ...
Studying fine-scale spatial genetic patterns across life stages is a powerful approach to identify e...
A total of 145 microsatellite primer pairs from Prunus DNA sequences were studied for transferabilit...
The utility of microsatellite markers to characterize the genetic diversity of a polyploid species w...
• Premise of the study: Microsatellites were designed and characterized in the African timber forest...
While the genetic structure of many tree species in temperate, American and Asian regions is largely...
Premise of the study: Multiplexes of nuclear microsatellite primers were developed to investigate po...
Premise of the study: Microsatellites were developed in the vulnerable African rainforest tree Afzel...
Refugia are expected to preserve genetic variation of relict taxa, especially in polyploids, because...
Premise Afzelia africana (Fabaceae) is a valuable, internationally vulnerable tree species in tropic...
Premise of the study: Multiplexes of nuclear microsatellite primers were developed to investigate po...
We developed eleven microsatellite markers for Hymenaea courbaril for the purposes of studying spati...
<p>Haplotype (cpSSR) (3a) and allelic (nSSR) (3b) richness are determined for 32 populations, after ...