Eryngium maritimum is a perennial species growing exclusively in a coastal littoral zone both on sand dunes and shingle beach and indicated as declining in Northern Europe. The objective of the present study was to prove the use of nondestructive physiological measurement methods to access physiological status of endangered plants, using E. maritimum as a model species. Plants from two Latvian sites were studied in comparison with other populations in Northern Europe (Estonia, Lithuania, Poland, United Kingdom) to find out if local differences in environmental factors affect vitality of E. maritimum individuals. Noninvasive chlorophyll analysis and chlorophyll a fluorescence measurements were used as indicators of plant physiological status through characterization of various aspects of photochemistry of photosystem II activity. Dynamics and morphology of individuals were investigated for evaluation of clonal growth potential of E. maritimum in natural conditions. Highly fluctuating trend of dynamics of individuals (within 40 groups at two Latvian sites) was established for E. maritimum in natural conditions over a five-year period. Disturbance of individuals lead to formation of new shoots from nodal root meristems. An exponential regression between fluorescence parameters F V /F M and Performance Index and summary monthly precipitation was found indicating that E. maritimum plants had significant tolerance to water shortage together with susceptibility to increased precipitation. Negative correlation between leaf chlorophyll content and more northern localization of individuals was found (r =0.95 and r = 0.94, for generative and vegetative shoots, respectively). Northern populations of E. maritimum are endangered by high precipitation in conditions of low air temperature, leading to decrease of photosynthetic productivity and overall physiological status. High developmental plasticity at the root level leads to clonal growth and an efficient survival and relatively long life span of E. maritimum individuals. Chlorophyll a fluorescence is a useful method to search for the effect of suboptimal conditions on physiological status of endangered plant species without elimination and disturbance of individuals.

The effects of season and cold storage on morphogenic competence in mature Pinus sylvestris buds were investigated. Peroxidase and polyphenol oxidase activity were measured as markers of oxidative metabolism. No growth in vitro was observed on explants detached from the end of January until the beginning of March. Brachioblasts, each with a couple of needles, formed on 11% of the buds without macrostrobili that were detached in early April and introduced immediately into culture. Of the explants detached in late July, 15% formed shoots with brachioblasts and needles. The lowest activity of peroxidase and polyphenol oxidase in pine buds was observed from the end of April until the beginning of June when morphogenic competence of tissues started to increase. Development of bud explants detached in January was achieved by cold storage for 5 months. Low polyphenol oxidase and peroxidase activity coincided with increased morphogenic potential. Results suggest that reduced or stable activity of peroxidase and polyphenol oxidase is associated with an increased ability of tissues to start growth in vitro.

The aim of the present paper was to show that differences in biological activity among commercially produced vermicompost samples can be found by using a relatively simple test system consisting of microorganism tests on six microbiological media and soilless seedling growth tests with four vegetable crop species. Significant differences in biological properties among analyzed samples were evident both at the level of microbial load as well as plant growth-affecting activity. These differences were mostly manufacturer- and feedstock-associated, but also resulted from storage conditions of vermicompost samples. A mature vermicompost sample that was produced from sewage sludge still contained considerable number of Escherichia coli. Samples from all producers contained several potentially pathogenic fungal species such as Aspergillus fumigatus, Pseudallescheria boidii, Pseudallescheria fimeti, Pseudallescheria minutispora, Scedosporium apiospermum, Scedosporium prolificans, Scopulariopsis brevicaulis, Stachybotrys chartarum, Geotrichum spp., Aphanoascus terreus, and Doratomyces columnaris. In addition, samples from all producers contained plant growth-promoting fungi from the genera Trichoderma and Mortierella. The described system can be useful both for functional studies aiming at understanding of factors affecting quality characteristics of vermicompost preparations and for routine testing of microbiological quality and biological activity of organic waste-derived composts and vermicomposts.

In order to test the hypothesis that arthropod-induced neoplastic formations on trees affect biochemical characteristics of both the newly formed galls and host plant tissues, biochemical characteristics with a possible adaptive role were determined in nine gall-former Á/host tree combinations. Photosynthetic pigments, extractable protein content, and oxidative enzyme activities were determined in gall tissues, leaf tissues of galled leaves, and leaves on ungalled tree branches. Neoplastic tissues were characterized by a low content of photosynthetic pigments, decreased chlorophyll a /b ratio, lower extractable protein content, and decreased activities of peroxidase and polyphenol oxidase as compared with ungalled host leaf tissues. In galled leaves or in leaves adjacent to galls, increased level of peroxidase activity was found. In several gall-inducer Á/host plant combinations, galled host plant tissues contained increased activity of polyphenol oxidase as well. The presented data reflect long-term systemic effects of neoplastic formation on host tree physiology suggesting that gall inducers affect potential adaptive responses of host plants.

Changes of morphogenic competence in mature P. sylvestris L. buds due to frozen storage were investigated. The highest callus formation was registered on explants stored at -18 °C for three months, but on explants stored for five months, it was also higher than in the control. Budding and development of needles in vitro was observed only for buds frozen three to five months. Peroxidase activity was lowest in these buds. In contrast, polyphenol oxidase activity in bud tissues continually increased during frozen storage. Within 10 months of frozen storage the content of starch and sugars in resting buds changed. It may be concluded that changes in composition of non-structural sugars in pine buds after five months of frozen storage are part of metabolic changes leading to loss of morphogenic capacity.