Now showing 1 - 2 of 2
  • Publication
    High outcrossing and random pollen dispersal in a planted stand of 'Acacia saligna' subsp. 'saligna' revealed by paternity analysis using microsatellites
    (Springer, 2008)
    Millar, MA
    ;
    Byrne, M
    ;
    Nuberg, I
    ;
    The mating system, patterns of pollen mediated gene flow and levels of genetic contamination were investigated in a planted stand of 'Acacia saligna' subsp. 'saligna' via paternity analysis using microsatellite markers. High levels of outcrossing were detected within the stand (tm=0.98), and the average pollen dispersal distance was 37 m with the majority of progeny sired by paternal trees within a 50-m neighbourhood of the maternal tree. Genetic contamination from the natural background population of A. 'saligna' subsp. 'lindleyi' was detected in 14% of the progeny of A. 'saligna' subsp. 'saligna' and varied among maternal trees. Long distance inter-subspecific pollen dispersal was detected for distances of over 1,500 m. The results provide information for use in the breeding and domestication programme aimed at developing A. 'saligna' as an agroforestry crop for the low rainfall areas of southern Australia.
  • Publication
    A rapid PCR-based diagnostic test for the identification of subspecies of 'Acacia saligna'
    (Springer, 2008)
    Millar, M A
    ;
    Byrne, M
    ;
    Nuberg, I
    ;
    Subspecific taxa of species complexes can display cryptic morphological variation, and individuals and populations can often be difficult to identify with certainty. However, accurate population identification is required for comprehensive conservation and breeding strategies and for studies of invasiveness and gene flow. Using five informative microsatellite markers and a Bayesian statistical approach, we developed an efficient polymerase chain reaction-based diagnostic tool for the rapid identification of individuals and populations of the 'Acacia saligna' species complex of Western Australia. We genotyped 189 individuals from 14 reference populations previously characterised based on morphology and used these data to investigate population structure in the species complex. High total genetic diversity (Ht=0.729) and high population differentiation (θ=0.355) indicated strong intra-specific structuring. With the provision of prior population information, the reference data set was optimally resolved into four clusters, each corresponding to one of the four main proposed subspecies, with very high membership values (Q>97%). The reference data set was then used to assign individuals and test populations to one of the four subspecies. Assignment was unequivocal for all test individuals from two populations of subsp. 'lindleyi' and for all but one individual of subsp. 'stolonifera'. Individuals from populations of subsp. 'saligna' and subsp. 'pruinescens' showed a degree of genetic affinity for the two subspecies in their assignments, although the majority of individuals were correctly assigned to subspecies. The diagnostic tool will assist in characterising populations of 'A. saligna', especially naturalised and invasive populations of unknown origin.