The macaw palm, Acrocomia aculeata (Jacq.) Lodd. ex Mart., is a Brazilian native species with great potential for biofuel production. The aim of this work was to analyze macaw palm genetic diversity to structure and assist in the definition of sampling strategies for germplasm banks. Forty-six microsatellite markers, from which seven polymorphic markers were used to evaluate 103 macaw palm individuals collected from different Brazilian locations. The polymorphic markers were used to generate a dissimilarity matrix by weighted index. The imaging of genetic variability was realized by 3D projection of matrix dissimilarity. Sixty-seven individuals had their ITS region sequenced and aligned, and the mutations found were used to generate a haplotype network. The average genetic distance identified between individuals was 76.2%, ranging from 3.7 to 100%. Genetic variability structure was not found. ITS region sequencing of the 67 individuals revealed four polymorphic sites, defining four haplotypes. The results of this study suggest that historically, macaw populations were strongly connected, indicating a recent population expansion of the species. The results indicate that macaw genetic variety sampling should focus on effective collection in selected locations. Areas such as Caatinga and Humid Chaco however, could present new sources of genetic variability, and should be studied.
The objective of this work was to determine the suitability of Setaria viridis as a model plant in studies to validate candidate genes for cold tolerance by evaluating the response of two of its accessions to different durations of abrupt or gradual cold stress in the vegetative and reproductive stages. Plants of accessions A10.1 and Ast-1, cultivated at 25°C, were subjected to the following cold stress treatments: gradual reduction in temperature from 25 to 0°C, 5°C at a time, every 24 hours in a same chamber; or abrupt reduction in temperature, by transferring plants from a chamber at 25°C to another at 0°C. Plants were kept at 0°C for 3, 5, or 10 days, after which temperature was increased back again to 25°C; a control group remained at 25ºC. Low temperatures – reduced abruptly or gradually – caused a decrease in the gas exchange rates and shoot and root biomass of the plants, besides damage to their photochemical apparatus; the longer the cold lasted, the more pronounced the effect was. Regardless of stress duration, plants recovered and completed their life cycle. The studied accessions are tolerant to cold and, therefore, are not suitable as a model plant in studies to validate candidate genes for cold tolerance.
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