The accumulation of trace metals in the shells of bivalves allows quantitative assessments of environmental pollution and helps to reconstruct paleo aquatic environments. However, the understanding on how marine and freshwater mollusks control the level of trace elements in their shells remains very limited. Here, we compared the trace element composition of marine and freshwater bivalves from boreal and subarctic habitats, using examples of widely distributed species of marine (Mytilus edulis, M. trossulus) and freshwater (Anodonta anatina, Unio sp., Beringiana beringiana) mussels. Sizable differences in several trace element concentrations were detected between different species, depending on their environmental niches. A multiparametric statistical treatment of the shell’s elemental composition allowed to distinguish the impact of external factors (water and sediment chemical composition) from active metabolic (biological) control. In particular, the obtained results demonstrated that Ba:Ca and Pb:Ca ratios in mussels’ shells are closely related to the primary productivity of aquatic ecosystems. The Mn:Ca ratio allowed to constrain the environmental conditions of mussels’ species depending on the trophic state of inhabited waterbody. Overall, the marine mussels exhibited stronger biological control of trace element accumulation, whereas trace element pattern in shells of freshwater mussels was chiefly controlled by environmental factors. The obtained results might help to use the trace element composition of bivalves in distinguishing marine and freshwater habitats of mollusks in paleo environments.

Sulfite and kraft pulping are two principal methods of industrial delignification of wood. In recent decades, those have been considered as possibilities to pretreat recalcitrant wood lignocellulosics for the enzymatic hydrolysis of polysaccharides and the subsequent fermentation of obtained sugars to valuable bioproducts. Current work compares chemistry and technological features of two different cooking processes in the preparation of polysaccharide substrates for deep saccharification with P. verruculosum glycosyl hydrolases. Bleached kraft and sulfite pulps were subjected to hydrolysis with enzyme mixture of high xylanase, cellobiohydrolase, and β-glucosidase activities at a dosage of 10 FPU/g of dry pulp and fiber concentration of 2.5, 5, and 10%. HPLC was used to analyze soluble sugars after hydrolysis and additional acid inversion of oligomers to monosaccharides. Kraft pulp demonstrated higher pulp conversion after 48 h (74–99%), which mostly resulted from deep xylan hydrolysis. Sulfite-pulp hydrolysates, obtained in similar conditions due to higher hexose concentration (more than 50 g/L), had higher fermentability for industrial strains producing alcohols, microbial protein, or organic acids. Along with saccharification, enzymatic modification of non-hydrolyzed residues occurred, which led to decreased degree of polymerization and composition changes in two industrial pulps. As a result, crystallinity of kraft pulp increased by 1.3%, which opens possibilities for obtaining new types of cellulosic products in the pulp and paper industry. The high adaptability and controllability of enzymatic and fermentation processes creates prospects for the modernization of existing factories.

It is suggested to use a binary solvent, 1-butyl-3-methylimidazolium acetate + dimethyl sulfoxide, for full dissolution of wood, followed by its separation into the polysaccharide and lignin...

Polysaccharide-based cryogels are promising materials for producing scaffolds in tissue engineering. In this work, we obtained ultralight (0.046–0.162 g/cm³) and highly porous (88.2–96.7%) cryogels with a complex hierarchical morphology by dissolving cellulose in phosphoric acid, with subsequent regeneration and freeze-drying. The effect of the cellulose dissolution temperature on phosphoric acid and the effect of the freezing time of cellulose hydrogels on the structure and properties of the obtained cryogels were studied. It has been shown that prolonged freezing leads to the formation of denser and stronger cryogels with a network structure. The incorporation of chitin nanowhiskers led to a threefold increase in the strength of the cellulose cryogels. The X-ray diffraction method showed that the regenerated cellulose was mostly amorphous, with a crystallinity of 26.8–28.4% in the structure of cellulose II. Cellulose cryogels with chitin nanowhiskers demonstrated better biocompatibility with mesenchymal stem cells compared to the normal cellulose cryogels.