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The assessment of the surface area of all leaves from a tree crown is regarded as one of the key parameters in scaling ecophysiological processes, such as growth, carbon budget, and water management. The purpose of this study was to investigate the variation of the mass and surface area of Scots pine needles, obtained from trees growing in the same habitat conditions but at different stock densities, therefore occupying different biosocial positions. The mass of needles and the leaf area index (LAI) were determined for an even-aged 33-year-old Scots pine stand located at a fresh mixed coniferous forest site in southwest Poland (50°32′ N; 17°42′ E). The needles, collected from all the sample trees, were subjected to a biometric analysis to determine the total mass of needles from each tree, the mass of 1000 needle pairs, the number of needles per crown, and the needle length distribution. Based on the actual measurements, we derived allometric equations for finding the fresh mass (FMN) and the surface area of the needles (SN), using the diameter at breast height (DBH) as an independent variable. The relationships between the mass of the needles and the DBH were significant (p < 0.0001), and so were those between the surface area of the needles and the DBH (p < 0.001). The fresh mass of needles for the tree stands varied from 6458 kg·ha−1 to 11,102 kg·ha−1. The LAI was in the range of 3.2 to 5.4 m2·m−2. The mean value of the LAI for the Scots pine stand was 4 m2·m−2. Further studies are required and more algorithms need to be developed for the quantitative assessment of the LAI in Scots pine trees, using a larger number of sample trees with more varied biometric features.

In the last ten years, many countries around the world recorded a new disease of the Cucurbitaceae, the agent of which was P. melonis. The ability of P. melonis 502 to form intracellular mycelium in the epidermal and parenchymal tissues of roots was shown. Leading tissues (xylem and phloem) did not colonize, which indicates the impossibility of plant vessel clogging and shows the fungus’s biochemical effects on plants, which causes the process of pathogenesis. P. melonis 502 is able to develop in a wide range of pH values, while the pH-optimum is 8.5. P. melonis 502 is able to adjust the pH of the medium to the optimal value—8.5. We also showed that cellulase enzyme synthesis depends on pH. We studied the exo-, endo- and β-glucasidase activity of P. melonis 502 and found that the highest activity of cellulase enzymes was on a medium whose pH was 8.5. In the process, the total cellulolytic activity was 0.326 U mL−1, exoglucanase activity—0.539 U mL−1, endoglucanase activity—0.950 U mL−1 and β-glucosidase activity—0.795 U mL−1.

The accumulation of various types of waste containing both organic and inorganic metal-containing compounds is extremely hazardous for living organisms. The possibility of polymer degradation, biohydrogen synthesis, and metal detoxification via the dark fermentation of model potato waste was investigated. For this purpose, the strict anaerobic strain was isolated and identified as Clostridium butyricum. The high efficiency of dark hydrogen fermentation of potatoes with yield of hydrogen in 85.8 ± 15.3 L kg−1 VSpotato was observed. The copperand chromium salts solutions were added to the culture fluid to obtain the concentrations of 50, 100, and 200 mg L−1 Cu(II) and Cr(VI) in the active phase of growth (19 h of cultivation). Metals at a concentration of 200 mg L−1 inhibited the fermentation process the most. The hydrogen yield decreased in 7.2 and 3.6 times to 11.9 ± 2.1 and 23.8 ± 5.6 L kg−1 VSpotato in the presence of 200 mg L−1 Cu(II) and Cr(VI), respectively. The efficiencies of the chromium bioremoval in all variants of the experiment were 100%, and those of copper bioremoval were about 90%. A pure culture of strict anaerobes Clostridium butyricum strain 92 was used for the first time for the detoxification of metals. The presented results confirmed the possibility of this promising strain application for industrial H2 production and the bioremediation of contaminated sites.

The aim of this study was the identification of the causative agent of the basal glume rot of wheat Pseudomonas syringae pv. atrofaciens from the affected weeds in wheat crops, and determination of its virulent properties. Isolation of P. syringae pv. atrofaciens from weeds of wheat crops was carried out by classical microbiological methods. To identify isolated bacteria, their morphological, cultural, biochemical, and serological properties as well as fatty acids and Random Amplification of Polymorphic DNA (RAPD)-PCR (Polymerase chain reaction) profiles with the OPA-13 primer were studied. Pathogenic properties were investigated by artificial inoculation of wheat plants and weed plants, from which bacteria were isolated. For the first time, bacteria that are virulent both for weeds and wheat were isolated from weeds growing in wheat crops. It was shown that the fatty acids profiles of the bacteria isolated from the weeds contained typical for P. syringae pv. atrofaciens fatty acids, in particular, hydroxy acids: 3-hydroxydecanoic, 2-hydroxydodecanoic, and 3-hydroxydodecanoic. RAPD-PCR profiles of the newly isolated strains were identical to those of the collection strains P. syringae pv. atrofaciens UCM B-1011 and P. syringae pv. atrofaciens UCM B-1014 and contained a dominant fragment of 700 bp. The isolated strains, according to their phenotypic and genotypic properties, were identified as P. syringae pv. atrofaciens. It was established that the causative agent of basal glume rot of wheat P. syringae pv. atrofaciens is polyphagous and capable of infecting a wide range of plants. The main control measure for cereals diseases caused by P. syringae pv. Atrofaciens&mdash, crop rotations with nonhost species, should be revised, and alternative control methods must be proposed.