This study was undertaken with the aim of investigating the effect of Cd 2+ and Ni 2+ containing solutions on selected physiological parameters (metal uptake, chlorophyll a fluorescence, assimilation pigment composition, thiobarbituric acid-reactive substance production, and ergosterol content) in the lichens Peltigera rufescens and Cladina arbuscula subsp. mitis growing on historic copper mine-spoil heaps at Ľubietová-Podlipa, Slovakia. Physiological measurements did not confirm significantly higher sensitivity to Cd and Ni of the cyanolichen P. rurescens compared to the green-algal lichen C. arbuscula subsp. mitis. Under natural conditions, C. arbuscula subsp. mitis is able to grow directly on copper mine heaps of Central Slovakia, while P. rufescens grows only on their margins. A crucial factor for this limited distribution of P. rufescens may be, at least in part, the higher intracellular accumulation of metals. Although lichen photobionts are generally regarded as key elements of lichen sensitivity, further research is necessary to elucidate this point since the higher levels of intracellular Cd and Ni do not allow to regard cyanobacterial photobionts of P. rufescens as more sensitive than the eukaryotic ones of C. arbuscula subsp. mitis.
In the present work, the long-term effect (14 days) of copper on the levels of intracellular and total copper accumulation, growth, assimilation pigment composition, chlorophyll a fluorescence, soluble protein content and oxidative status (production of hydrogen peroxide and superoxide) in two algal species (Scenedesmus quadricauda and Trebouxia erici) was assessed. Scenedesmus quadricauda is a free-living alga while Trebouxia erici is the photobiont of a lichen. The presence of copper negatively affected growth, assimilation pigments, chlorophyll a fluorescence, soluble protein content and oxidative status in both the algae. However, Scenedesmus was much more sensitive compared to Trebouxia.
We used flow cytometry (FCM) to investigate genome size variation in two polymorphic allopolyploids, Onosma arenaria Waldst. and Kit. and O. pseudoarenaria Schur, in Central Europe and the Balkan Peninsula. An intercalating DNA stain, propidium iodide (PI), and internal standardization were used. Our data showed that cytosolic compounds may be present in FCM samples and could inhibit, or more frequently promote, PI intercalation. In the absence of PI intercalation interference, leaf-based genome size estimates were observed to be lower than seed-based ones in O. pseudoarenaria, whereas no difference was recorded in O. arenaria. In incubation tests, genome size values frequently increase after a longer staining period. For final genome size measurements, we applied the FCM protocol based on seed material using a ∼150 min incubation period, and provide evidence of mean genome size variation among populations of both species. Two and four natural genome size groups were revealed in O. arenaria and O. pseudoarenaria respectively. Group mean genome sizes varied considerably in both O. arenaria (5.36–5.76 pg) and O. pseudoarenaria (5.98–6.58 pg). This extensive genome size variation is attributed to unexplored taxonomic heterogenity in both taxa. Future taxonomic revision of the group may be supported with genome size measurements obtained using an appropriately standardized methodology.
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