The phylogenogeographic structure, polymorphism, and differentiation of Pinus sylvestris L. have been studied for the first time by means of allozyme analysis of 143 populations along a network of transects covering the entire species range. The results show that the species in general is characterized by a significant level of differentiation, regardless of its relative uniformity in northern and central parts of the range. Nei's genetic distances between populations and their gradients in the extreme southern parts of the range, where it has an insular pattern, are seven to eight times greater than in the northern, "glacial" zone. Three Pleis tocene refugia for the species have been revealed in the Balkans, Southern Urals, and Northern Mongolia. Using analysis of genetic distances between 18 phylogeographic regions and an original genosystematic scale, one subspecies, five geographic races and nine geographic population groups have been distinguished in the P. sylvestris L. species structure.

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Metabolic profiling of cell line and tissue extracts involves sample processing that includes a drying step prior to re-dissolving the cell or tissue extracts in a buffer for analysis by GC/LC-MS or NMR. Two of the most commonly used drying techniques are centrifugal evaporation under vacuum (SpeedVac) and lyophilization. Here, NMR spectroscopy was used to determine how the metabolic profiles of hydrophilic extracts of three human pancreatic cancer cell lines, MiaPaCa-2, Panc-1 and AsPC-1, were influenced by the choice of drying technique. In each of the three cell lines, 40–50 metabolites were identified as having statistically significant differences in abundance in redissolved extract samples depending on the drying technique used during sample preparation. In addition to these differences, some metabolites were only present in the lyophilized samples, for example, n-methyl-α-aminoisobutyric acid, n-methylnicotimamide, sarcosine and 3-hydroxyisovaleric acid, whereas some metabolites were only present in SpeedVac dried samples, for example, trimethylamine. This research demonstrates that the choice of drying technique used during the preparation of samples of human cell lines or tissue extracts can significantly influence the observed metabolome, making it important to carefully consider the selection of a drying method prior to preparation of such samples for metabolic profiling.

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