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The level of polymorphism, genetic variability and relatedness of the Antarctic hairgrass Deschampsia antarctica Desv. Populations from South Shetlands Is. (King George I., Penguin I., Livingstone I.), from vicinity of Antarctic Peninsula (Galindez I., Uruguay I.), and Falklands Is. (Jason Is., Sealion I.) were studied using the AFLP approach. Six EcoRI/MseI type selective primer pairs combinations were used for AFLP profiling and amplified scoreable DNA fragments; than AMOVA and PCA were performed. The level of molecular variability among all individuals from all the analysed populations was low and reach only 5.4 % irrespective of the distance between the localities and it was not significant at a broader geographical scale, even among the three groups of populations (South Shetlands Is., vicinity of Antarctic Peninsula, and Falklands Is.). PCA analysis shows that all populations formed uniform groups according to their locations.
Deschampsia antarctica Desv. plants collected on King George Islands (Antarctica) at two localities that differ in topographic and nutrition conditions exhibited morphological variation that differentiated plants of both locations. The molecular variation characteristic to individuals of both sites was tested using AFLP approach in order to verify whether morphological variation characteristic to the plants resulted from environmental factors or possibly from differences at the DNA level. Four primer pair combinations were used to generate 339 AFLP fragments, 132 of which were polymorphic and allowed evaluation of genetic relationships among D. antarctica individuals. Chi-square test revealed that only 12 signals were discriminative for the plants from both locations. Cluster analysis conducted on these AFLP fragments demonstrated that plants from the location rich in biogenes were more polymorphic than those from poor one. Our data suggest that the phenotypic variation specific to plants of both locations seem to be the result of adaptation to the environmental conditions like soil and moisture rather than reflect genetic differences.
Eight to nineteen ethanol-soluble carbohydrate components were identified in vegetative tissues of Colobanthus quitensis and Deschampsia antarctica. The analysed carbohydrates included: monosaccharides, cyclitols, galactosyl cyclitols, raffinose family oligosaccharides, lichnose family oligosaccharides, kestose family oligosaccharides. The analysed vegetative tissues accumulated from 447 to 139 mg/g d.m. soluble carbohydrates in Colobanthus quitensis, Deschampsia antarctica respectively. The raffinose family oligosaccharides constituted 53.3% in Colobanthus quitensis of the identified soluble carbohydrate component pool. Vegetative tissues accumulated starch in Colobanthus quitensis 20.6 mg/g d.m. and 261.6 mg/g d.m. in Deschampsia antarctica. Anatomical and ultrastructural observations of vegetative part of Colobanthus quitensis and Deschmpsia antarctica revealed the presence of various ergastic materials in intercellular spaces, cell walls and protoplasts. Various parts of these plants contain insoluble, PAS positive polysaccharides in intercellular spaces and in cell walls. Chloroplasts of analysed tissues contained starch. Less starch was visible in young, growing parts of shoots of Colobanthus quitensis and Deschmpsia antarctica, more starch appears in mature, differentiated parts.
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