The impact of heat shock on minimising the activity of photosystem 2 (PS2) initiating high lipid peroxidation (POL) level and consequently changes in the enzymatic-antioxidant protective system was studied in seedlings of two Egyptian cultivars of barley (Giza 124 and 125). Heat doses (35 and 45 °C for 2, 4, 6, and 8 h) decreased chlorophyll (Chl) contents coupled with an increase in Chl a/b ratio, diminished Hill reaction activity, and quenched Chl a fluorescence emission spectra. These parameters reflect the disturbance of the structure, composition, and function of the photosynthetic apparatus as well as the activity of PS2. POL level, as dependent on the balance between pro- and anti-oxidant systems, was directly correlated with temperature, exposure time, and their interaction. Heat shock caused an increase in the electric conductivity of cell membrane, and malonyldialdehyde content (a peroxidation product) coupled with the disappearance of the polyunsaturated linolenic acid (C18:3), reflecting the peroxidation of membrane lipids which led to the loss of membrane selective permeability. Moreover, it induced distinct and significant changes in activities of antioxidant enzymes. Superoxide dismutase and peroxidase activities have been progressively enhanced by moderate and elevated heat doses, but the most elevated one (45 °C for 8 h) showed a decrease in activities of both enzymes. In contrast, catalase activity was reduced with all heat shocks. and F. El-Shintinawy ... [et al.].
The development of Myxobolus dispar Thélohan, 1895, a myxosporean parasite of the gills of common carp (Cyprinus carpio L.) was studied in experimentally infected oligochaetes Tubifex tubifex Muller. After infection of uninfected tubificids with mature spores of M. dispar, development of actinosporean stages was first observed light microscopically 21 days after initial exposure. In histological sections, early pansporocysts were located in the gut epithelium of experimental oligochaetes, while advanced stages occupied mostly the outer layers of the gut and the coelozoic space. Mature pansporocysts, each containing 8 raabeia spores, appeared 199 days after initial exposure. Following damage of the intestinal wall and rupture of the pansporocysts, free actinosporean stages were found in the gut lumen of the oligochaetes. Actinospores of hi. dispar emerged from the worms after 217 days of intra-oligochaete development. They were floating in the water and showed a unique raabeia form. Each raabeia spore had three pyriform polar capsules and a cylindrical-shaped sporoplasm with approximately 32 secondary cells. The spore body joined the three caudal projections without a style. Caudal projections were bifurcated at the end and the two main branches had further small bifurcations. The total length of the raabeia spore was approximately 158 pm. The prevalence of infection in 240 experimentally infected Tubifex specimens was 99.2%. No infection was found in the control oligochaetes.
Ribulose 1,5-bisphosphate carboxylase/oxygenase (RuBPCO) and RuBPCO binding protein (BP) were isolated from barley leaves. RuBPCO was dissociated into subunits under denaturing conditions. Polyclonal antibodies against RuBPCO, RuBPCOBP and RuBPCO large subunit (LS) were raised. Inununoblotting analyses showed that anti-RuBPCO antibodies did not cross-react with BP. Anti-BP antibodies cross-reacted with RuBPCO smáli subunit (SS) and reacted but more slightly with RuBPCO LS.
Characteristic features of stomatal apparatus, i.e, stomatal density, area of the stomatal poruš, relative stomatal area and diffusion resistance (r^) were examined in young (10 d) and old (30 d) leaves of four sugar beet cultivars (Allyx, Arigomono, Monohil and Primahill). Since the plant age was also considered to be an important ontogenetic factor, all measurements were repeated at plant ages of 40, 47, 57 and 65 d. Genotypical differences among the cultivars studied could be explained in terms of the level of ploidy, i,e. an increasing number of chromosome sets was accompanied by an increase of stomatal size and a decrease of stomatal density. The other stomatal characteristics did not significantly differ among the cultivars. The increase in plant age resulted in a higher stomatal density and a gradually decreasing stomatal size. These phenomena generally induced a plant ontogeny controlled increase of the relative stomatal area of all leaf series. Young leaves showed higher stomatal densities, but the stomata were smaller and póre area was reduced by 40 to 60 %, compared to the old leaves. The young leaves also exhibited a smaller r^.
We set up axioms characterizing logical connective implication in a logic derived by an ortholattice. It is a natural generalization of an orthoimplication algebra given by J. C. Abbott for a logic derived by an orthomodular lattice.
The ultrastructure of the endogenous stages - merozoites, microgamonts, macrogamonts and oocysts, of Sarcocystis muriviperae from the snakes Vipera palaestinae and Coluber jugularis is described. Snakes were infected via white mice fed on sporocysts obtained from naturally infected snakes of the same species. Snakes examined 4 days post-infection contained only young and premature gamonts. Infection in snakes sacrificed on day 7 post-infection consisted predominantly of mature microgamonts and macrogamonts; snakes examined on day 10 post-infection revealed only oocysts. The fine structure of the endogenous stages from the two snakes, including size and contents of the wall-forming bodies, was identical, confirming their suggested conspecificity. Observed endogenous stages also conformed in their major details with the same developmental stages of other Sarcocystis species studied from other snakes and mammalian definitive hosts and from in vitro culture. However, they differed from the latter in size and contents of the wall-forming bodies. The observed fertilization process was reminiscent of that described earlier in S. bovicanis.