Climate changes influencing forest ecosystems include increased air temperatures and CO2 concentrations as well as droughts and decreased water availability. These changes in turn effect changes in species composition of both host plants and pathogens. In the case of Armillaria, climate changes cause an increase in the activity of individual species and modify the growth of rhizomorphs, increasing the susceptibility of trees. The relationship between climate changes and the biotic elements of Armillaria disease are discussed in overview.
As recently reported, European mistletoe has become an important agent of damage to forest trees in Central Europe. To document the extent of its impact, host and environmental preferences, as well as spatial and temporal dynamics, we have analyzed the results of 10 years of annual assessments of tree damage in level 1 plots of country-wide national forest monitoring. Mistletoe was found on 12 forest tree species, most frequently on silver fir and Scots pine, much less often on birches and deciduous admixture species. Common beech, pedunculate, and sessile oaks, as well as coniferous admixture species, were found to be free from the parasite. Mistletoe was more common on larger trees, mainly those in the 1st and 2nd Kraft classes, characterized by a higher DBH value than trees without V. album. Infestation was also age-dependent with low numbers of infested trees in young age classes and a much higher proportion of infested trees being over 80–100 years in age. Defoliation of trees colonized by mistletoe was found to be significantly higher than in trees free from the parasite, confirming the adverse effect of infestation on tree health. The increase of relative incidence of tree infestation by mistletoe in forests in Poland was high throughout the entire period 2008–2018 and significant for the most threatened host species: silver fir, Scots pine, and birches. It was also found that spread direction was from west to east and that the occurrence of V. album shows clear regionalization. The most endangered forests were located within a 200 km wide zone ranging through lowland Central Poland from the border with Germany down to the border with Ukraine and Belarus. The highest concentration occurred in the Western part of the country. Outside this zone (to the north and south) the mistletoe was much less abundant as expressed by the amount of injuries caused by the parasite or infested trees per plot.
The activity of cellulase, peroxidase, phosphatase and dehydrogenase enzymes, together with the content of protocatechuic and vanillic acids, in samples of Norway spruce wood inoculated with 17 different isolates of Phlebiopsis gigantea was measured. The same isolates were used to compare decay activity in samples of Norway spruce wood after incubation for 3 and 6 months. Significant differences in enzyme activity and phenol production were found between aerial mycelium overgrowing the wood sample and the underlying wood. These differences indicated that the nature of the fungal mycelium appears to change depending on whether it is in contact with wood. After 6 months, highly extensive decomposition of the wood was shown by two British isolates. The results confirm a large difference in P. gigantea inoculum among isolates in natural conditions and reinforce the need for constant evaluation of the most active isolates to use in preparations for biocontrol: a problem for both users and registration bodies.
The goal of the current study was to evaluate the efficiency of Norway spruce wood decomposition by the saprotrophic fungus Phlebiopsis gigantea (Fr.) Jülich. We identified the following indices as reliable measures of wood decay: decay acceleration index (DAI), final decay index (FD), and decay intensity index (DI). DAI was used to assess acceleration and deceleration of spruce wood loss, FD to estimate the final wood decay, and DI to evaluate the ability of the fungus to decompose wood, taking into consideration changes in mycelial activity over time. We tested the hypothesis that the wood decay activity of any fungus can be evaluated more objectively when: (i) several isolates of the tested fungus are assessed simultaneously, (ii) tests are performed for at least two time-points, and (iii) samples vary in wood density. Allowing a three-month period for wood decomposition was inadequate for reliable assessment of the wood decay ability of P. gigantea. Conversely, six months after inoculation, the tested isolates showed significant differences in their ability to generate dry wood loss, which depended on wood density. In view of these results, the DAI, FD, and DI indices are practical tools for assessing fungal activity to predict wood loss.
Initial experiment was made in order to test wood-decomposing fungus Phlebiopsis gigantea for enzymatic activity. Laccase, peroxidase, cellulase, phosphatase, dehydrogenase were marked using different methods for P. gigantea isolates growing on Scots pine wood.