Cosmopolites sordidus (Germar), commonly known as banana corm weevil, is an important economic pest in Asia that can cause severe yield loss depending upon the stage at which infestation occurs. In spite of its economic importance, little is known about the population structure of this pest in India. Random amplified polymorphic DNA (RAPD) and amplified fragment length polymorphism (AFLP) were used to characterize the population genetic structure of C. sordidus collected from five hot spot locations in India. Nineteen RAPD primers and five selective AFLP primer combinations generated 147 and 304 amplification products, respectively. UPGMA dendrograms generated with both marker systems failed to reveal populations clustered based on geographic distance, which was confirmed by the Mantel test, which did not show a strong correlation between genetic distance and geographic distance. Values of indices of genetic identity showed that the populations were closely related. Though the gene flow estimate (Nm) between the populations was 0.469, suggesting restricted gene flow, the populations are not genetically distinct. These observations suggest that the range expansion of this banana pest in India has taken place through transport of infested corms and plant material, resulting in genetically close populations that are geographically distinct. These results provide important information on the population structure of this pest in India, which will aid in designing suitable strategies for its control and management, especially with respect to insecticide resistance.

Levels of inter- and intrapopulation genetic variation were determined in five North American populations of leafy spurge using chloroplast DNA (cpDNA) RFLPs and RAPD markers. Thirteen plastome types were identified among 123 individuals collected from five geographically separated populations. Number of plastomes within a population ranged from one to seven, with four of the populations having a predominate type plus one or more rarer types. Some plastome types were shared by populations, but plastome distribution among populations was nonrandom. RAPD markers indicated greatest relatedness among individuals within a population. Relatedness among populations as established through RAPDs was greater for geographically closer populations; this relationship was not observed for cpDNA markers. Differences in the range of movement for pollen and seed may account for differences between results of the cpDNA and RAPD analyses. The high degree of genetic variability among North American leafy spurge suggests possible multiple introductions or a high degree of variability within leafy spurge populations in its native range.

Genetic markers have been used in horticulture and conservation biology to identify breeding lines, assess genetic diversity, and examine gene flow. In weed science, analysis of genetic markers is not as common, as the focus often lies in the development of control methods. This is unfortunate, because advances in genetic marker techniques may lead to innovative methods in controlling weedy plants. Microsatellites, random amplified polymorphic DNA (RAPDs), intersimple sequence repeats (ISSRs), amplified fragment length polymorphisms (AFLPs), DNA sequences, single nucleotide polymorphisms (SNPs), and derived cleaved amplified polymorphic sequences (dCAPS) have been used in studying genetics of weedy plants. Beyond assessing genetic diversity of weeds, markers have been used to examine gene flow, patterns of dispersal, ploidy levels, and relationships of weedy and nonweedy species, as well as identifying founder populations. Identification of closely related species may indicate the potential for hybridization, cross reactivity of chemical applications, or nontarget biological control effects. Furthermore, markers have been used in identification of mutations conferring herbicide resistance and identification of regions correlating fitness of weedy and hybrid plants in new habitats. Knowledge from genetic markers provides fundamental information that can be used in advancing chemical and biological control in weed management. This article serves as a review of these marker types and their application to weed science.

The capacity of the polar flora to adapt is of increasing concern given current and predicted environmental change in these regions. Previous genetic studies of Antarctic mosses have been of limited value due to a lack of variation in the markers or non-specificity of the methods used. We examined the power of five microsatellite loci developed for the cosmopolitan moss Ceratodon purpureus to detect genetically distinct clones and infer the distribution of clones within and among populations from the Windmill Islands, East Antarctica. Our microsatellite data suggest that the extraordinarily high levels of variation reported in RAPD studies were artificially elevated by the presence of contaminants. We found surprisingly little contribution of asexual reproduction to the genetic structure of the Windmill Islands populations, but more loci are required to determine the distribution of individual clones within and among populations. It is apparent that Antarctic populations of C. purpureus possess less genetic diversity than temperate populations, and thus have less capacity for adaptive change in response to environmental variation, but more markers are needed to resolve the total genetic diversity in Antarctic C. purpureus and other mosses.

Allozyme and Random Amplified Polymorphic DNA (RAPD) variation was surveyed in the freshwater crayfish Cherax destructor Clark, an ecologically and commercially important species that is widespread throughout the freshwater systems of central Australia. At the intra-population level, allozymes revealed a similar level of variation to that found in other freshwater crayfish; RAPDs showed less diversity than allozymes, which was unexpected. At the inter-population level, both techniques revealed significant population structure, both within and between drainages. RAPD results were consistent with phylogeographic patterns previously identified using mtDNA. Although allozyme data showed little geographic pattern in relation to genetic variation based on multidimensional-scaling (MDS) plots on matrices of genetic distance, results of AMOVA and Mantel tests indicated significant population structuring. Each of the mtDNA lineages proposed in a previous study also showed significant genetic structure at similar levels as revealed by RAPDs but different levels by allozymes. These results reject hypotheses previously put forward on genetic homogenisation within the species due to wide-scale translocation. The implications of the findings for conservation and aquaculture of C. destructor are also discussed.

Mount Melbourne in northern Victoria Land, Antarctica, is a glaciated 2733 m volcanic cone. The moss Compylopus pyriformis occurs on two small areas of steam-warmed snow-free ground near its summit. This moss species also occurs in temperate regions world-wide, but has not been recorded elsewhere in continental Antarctica. RAPD (Random Amplified Polymorphic DNA) studies of 26 samples of C. pyriformis from two areas of heated ground on Mount Melbourne showed there was genetic diversity within the population. Genetic evidence for dispersal between the two sites, together with some genetic variation within individual colonies, indicates a single colonisation event has probably occurred at this extremely isolated location followed by multiple mutations. A single sample of moss protonema was collected 25 years ago from steam-warmed ground near the summit of another volcano, Mount Erebus (3794 m), on Ross Island some 300 km south of Mount Melbourne. The moss could not be identified based on morphological and reproductive criteria, as all attempts to differentiate it to a recognisable gametophyte were unsuccessful. The RAPD technique has now shown it to be C. pyriformis, and closely related to the population on Mount Melbourne.

The threatened Chilean conifer Podocarpus salignus D. Don is currently the focus of ex situ conservation eorts being undertaken by the Conifer Conservation Programme of the Royal Botanic Garden Edinburgh. To assess variation within in and ex situ populations of the species, leaf material collected from four wild populations was analysed by random amplified polymorphic DNA (RAPD). Amova of RAPD profiles indicated that 93% of the variation occurred within, rather than between, populations. Intraspecific genetic diversity, estimated using percentage polymorphic loci, Shannon's diversity index, and Nei's gene diversity, was relatively high (47%, 0.692 and 0.314, respectively). To assess genetic diversity in ex situ populations within the UK, RAPD analysis of parents and progeny at two Cornish arboreta was undertaken. The results provided evidence of novel hybridization with suspected paternal trees (P. hallii Kirk and P. totara G. Benn. ex D. Don) endemic to New Zealand. RAPD was found to be an effective tool for assessing the genetic structure of P. salignus, for providing a guide to future germplasm-sampling strategies, and for hybrid identification. Implications for genetic conservation of the species and the role of ex situ approaches are discussed.

Random amplified polymorphic DNA (RAPD) markers were used to quantify genetic diversity within and between 5 populations of Schistosoma mansoni within its definitive host (Rattus rattus) and the 5 corresponding populations of the snail intermediate host (Biomphalaria glabrata) from a limited endemic area of murine schistosomiasis on the island of Guadeloupe. Analysis of molecular variance (AMOVA) and canonical correspondence analysis (CCA) were used to test the significance of genetic differentiation between populations. Both methods gave similar results. Of total gene diversity, 15.1% (AMOVA) and 18.8% (CCA) was partitioned between localities for S. mansoni with an absence of association between genetic and geographical distances. Geographical localities accounted for 20.5% (CCA) of the total diversity for B. glabrata populations. The genetic distances between pairs of parasite populations were not correlated with the genetic distances between the corresponding pairs of snail host populations. Such strong patterns of local differentiation of both parasite and snail populations are consistent with predictions based on metapopulation dynamics and may have implications on host–parasite susceptibility relationship through local adaptation processes.

The genetic population structures of the freshwater snail Bulinus globosus and its trematode parasite Schistosoma haematobium from 8 river sites in the Zimbabwean highveld were compared using randomly amplified DNA(RAPD) markers. There was significant variability between snail populations collected at different sites, but schistosome populations only showed differentiation at a wider geographical scale (between 2 non-connected river systems). For snails, genetic distance was better correlated with proximity along rivers than absolute geographical separation. In contrast, schistosome genetic distance was better correlated with absolute geographical separation than proximity along rivers. These results are consistent with different dispersal mechanisms for snails and schistosomes and the implications for host–parasite coevolution are discussed.

Fitzroya cupressoides (Molina) Johnston (Cupressaceae), a threatened conifer native to southern South America, has been cultivated in a number of gardens and arboreta in the British Isles since its introduction in 1849. In order to assess the importance of these cultivated trees for ex situ conservation, foliar samples were collected from 48 trees from throughout the British Isles, including five of known wild origin (Chile). DNA was extracted from these samples and assessed using the RAPD technique, in order to examine the extent of genetic variation. All samples from the cultivated trees of unknown origin, with one exception, were found to be genetically identical. In contrast, the five samples of known wild origin revealed pronounced polymorphism, varying from 5.3% to 49.1% between individuals. These results suggest that virtually all of the F. cupressoides trees currently cultivated in the British Isles have been derived from a single individual by vegetative propagation. Their value for ex situ conservation is therefore likely to be extremely limited. The implications of these results for the genetic conservation of other taxa in gardens and arboreta is discussed.