The quality of the aquatic environment and macrophytes of karstic watercourses

The quality of the aquatic environment and macrophytes were surveyed in the case of the remarkable karstic river Ljubljanica s. lat. (Slovenia). It consists of seven intermittent and permanent surface watercourses, connected by groundwater flows. We assessed 11 parameters describing the land use beyond the riparian zone, the structure of the riparian zone and stream channel morphology, as well as the distribution and abundance of macrophytes. The intermittent watercourses exhibited a relatively high level of naturalness, because the variable water regime prevents intensive human activity. Greater influence of the human activity on the permanent watercourses resulted in a modified riverine environment. The share of different ecological groups of macrophytes, i.e. submerged, emerged and amphibious species, reflected the water regimes of the different watercourses. A total of 62 taxa of macrophytes were identified in about 100 km of length examined. Of these, amphibious macrophytes dominated as a consequence of intermittent water regime. The relationship between environmental parameters and macrophytes, and the effects of the intermittent hydrology were investigated. All environmental parameters explained 28% of the variance in the distribution of macrophytes in watercourses, as determined by canonical correspondence analysis. Completeness of the riparian zone, bank undercutting and sediment accumulation were found to be the most influential.     

Jurassic neptunian dikes at Mt Mangart (Julian Alps,NW Slovenia)

Jurassic neptunian dikes are common within Upper Triassic to Lower Jurassic platform limestone of the Julian Alps. At Mt Mangart, the following geometries were observed: irregular dissolution cavities, thin penetrative fractures, larger fractures with sharp sidewalls, and laterally confined breccia bodies. Inside a complex neptunian dike system two main generations of infillings were differentiated. The first generation is heterogeneous and consists of bioclastic limestones, representing uniquely preserved sediments subdivided into five different microfacies. The second generation is more common and typically consists of coarse-grained breccias with host-rock clasts and marly limestone matrix containing echinoderms. Fracture formation and void filling of the first generation of neptunian dikes is dated as Pliensbachian and is interpreted to be caused by the Julian carbonate platform dissection due to widely recognized Lower Jurassic Tethyan rifting. The timing of formation for the second generation is only broadly constrained, ranging from the Pliensbachian to the Late Cretaceous.     

Therapy effect of antiulcer agents on new chronic cysteamine colon lesion in rat

After demonstration that cysteamine induced duodenal lesions in gastrectomized rats, while a number of antiulcer drugs mitigated these lesions, it was shown that one single intrarectal (i.r.) cysteamine application produced severe colon lesions in acute studies in rats. Thus, the further focus was on the protracted effect of cysteamine challenge (400 mg/kg b.w. i.r.) and therapy influence in chronic experiments in female rats. Regularly, cysteamine colon lesions were markedly mitigated by ranitidine (10), omeprazole (10), atropine (10), methylprednisolone (1), sulphasalazine (50; mg/kg), pentadecapeptide BPC 157 (PL-10, PLD-116; 10 microg or 10 ng/kg). Specifically, after 1 or 3 months following initial challenge (cysteamine 400 mg/kg i.r.) in female rat, the therapy [BPC 157 (PL-10, PLD-116 (10.0 microg or 10.0 ng/kg; i.g., i.p., i.r.), ranitidine, omeprazole, atropine, methylprednisolone, sulphasalazine (i.p.)] reversed the protracted cysteamine colon injury: the 1 week-regimen (once daily application) started after 1 month post-cysteamine, as well as the 2 weeks-regimen (once daily application), which started after 3 months. The effect on recidive lesion was also tested. These cysteamine lesions may reappear after stopping therapy (after stopping therapy for 3 weeks at the end of 2-weeks regimen started in 3 months-cysteamine female rats) in sulphasalazine group, while this reappearance is markedly antagonized in pentadecapeptide BPC 157 (PL-10, PLD-116)-rats (cysteamine-colon lesion still substantially low).