| Summary: | PROBLEM DEFINITION Genetic exchange between local populations of Deschampsia Antarctica (Poaceae), one of the two phanerogams occurring in Antarctica, might be difficult. Dispersal of the species within and between vegetated areas is believed to be via rain splash and via birds, collecting tufts of the species for nesting material, thus facilitating both vegetative and generative dispersal, but this is probably of local importance only. Its long distance dispersion is unclear. And yet, the species has a large distribution area, ranging from the frigid Antarctic to oceanic and alpine habitats. A marked increase in numbers of individual plants in established populations, as well as a vigorous colonization of recently deglaciated areas over the last four decades has been reported. Recent publications report also vigorous flowering, as well as abundant seed set and presence of seedlings throughout its distribution area, often attributed to parameters of global change, especially temperature increase. The fact that the species becomes more reproductive with increasing temperature could be either a plastic response, or selection for more reproductive genotypes under a changing temperature regime, or both. The role of genetic variation and phenotypic plasticity in the adaptation of Deschampsia Antarctica to increasing temperatures and its recent colonization of deglaciated areas is the aim of this study. APPROACH Using molecular techniques, the genotypic variation of D. Antarctica will be established in living samples and samples taken from herbarium specimens. From herbarium material only chlorophyll DNA can be successfully analyzed. Fresh material will be collected and preserved for the collection of nuclear DNA. Within and between population variability will be studied at the genotypic level using the overall AFLP fingerprint similarity as well as at the gene level, assuming Hardy Weinberg equilibriums (Schneider et al. 2000). Chloroplast DNA variation will be investigated using universal primers and digestion with restriction enzymes. This will provide phylogenetic analysis of the regions (phylogeography) and possibly allow a reconstruction of historical colonization patterns. The amount of nuclear DNA will be determined by flow cytometry of fresh material in different populations as this may affect the duration of the life cycle (Bennett et al, 1982). Genotypic variation and phenotypic plasticity in reproductive traits will be determined by growing cloned plant-genotypes from different populations under a set of environmental (temperature, moisture) circumstances and measure generative traits. Differences in the response of genotypes or populations to these environmental conditions would indicate within- or among population variation in reproductive traits.
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