Physiological Changes in Phaseolus vulgaris in Response to Long-term Ozone Exposure

The effects of ozone on Phaseolus vulgaris cv. Lit were investigatedusing open-top chambers (OTCs) ventilated with charcoal andPurafil filtered air (CF treatments), ambient air (NF treatments)and ambient air to which low, medium or high concentrationsof ozone were added (NFL, NFM and NFH). Ozone additions of 8,16 and 23 nl l^–1 were made during phase 1 of the experiment(0–44 d after emergence, DAE), and additions of 15, 30and 47 nl l^–1 were made during phase 2 (45–99 DAE).Ozone was added to the chambers between 1100 and 1800 h GMT,for 3 or 4 consecutive days each week. The seasonal 7-h meanozone concentrations were 8, 21, 27, 33 and 38 nl l^–1in the CF, NF, NFL, NFM and NFH treatments, respectively. No visible symptoms of ozone injury or significant physiologicalchanges were detected in P. vulgaris during phase I of the experiment.In phase 2, the photosynthesis (Pn) and stomatal conductance(gs) of NFH-plants were inhibited by 73% and 86%, respectively,during ozone exposure, and recovered to pre-exposure valueson the following day. These observations were made prior tothe appearance, 60 DAE, of bronze lesions on the leaves of NFH-plants.The photosynthetic capacity and gs of NFH-leaves decreased asthe severity of ozone injury increased. Rates of weight lossfrom excised leaves also increased with increasing ozone injury.Microscopic investigations of the bronzed regions revealed extensivecellular breakdown, including tonoplast and chloroplast enveloperupture, and the aggregation of the cytoplasmic contents towardsone end of the cell. Severely damaged leaves abscised from the plants, resultingin premature canopy senescence in the NFM and NFH treatments.This, coupled with the lower photosynthetic capacity of existingleaves led to 25 % lower yield in the NFH than the NF treatment(P < 0.05). Phaseolus vulgaris, green bean, ozone, symptom development, photosynthesis, cell ultrastructure     

The detection of apple chlorotic leafspot virus by a modified procedure of enzyme-linked immunosorbent assay (ELISA)

The technique of enzyme-linked immunosorbent assay (ELISA) was modified to enable detection of apple chlorotic leafspot virus (CLSV) both in herbaceous hosts and in several naturally infected fruiting and ornamental woody host species. Some of the characteristics of the modified method as used with different virus-host combinations are described.     

Fire behaviour and the invasion of Acacia sieberiana into savanna grassland openings

Following the recent decline in browsing and grazing pressures and changed fire regimes in Queen Elizabeth National Park, Uganda, Acacia thickets have encroached on grassland habitats important for grazing mammals. The objective of this research was to test experimentally the effects of fire behaviour, using simulated and natural fuel loading conditions, on A. sieberiana seedling and sapling regeneration. A high fire intensity (3200 kW m^-1) in natural fuels stimulated high seedling emergence (172 seedlings m^-2) compared to 6 seedlings m^-2 without fire. Also a highly significant linear regression was established between percentage top-kill of seedlings and fire intensities. High fire intensities during late dry season fires were more effective in controlling sapling height growth than early dry season fires of low intensities. A conceptual diagram was developed to show the major factors and possible pathways leading to successful invasion by A. sieberiana into grassland openings of the savanna.     

Do pollinators influence seed-set in Banksia paludosa Sm. and Banksia spinulosa R. Br.?

The consequences of observed variations in pollinator activity for plant reproduction depend on the breeding system of the plant and also on whether pollination is a resource in short supply. These factors are frequently assumed rather than tested. In bagging experiments with Banksia paludosa in heath and B. spinulosa var. spinulosa in woodland, the present study demonstrated that seed-set does not occur by autogamy and that pollinators are indeed necessary. Experimental addition of outcrossed pollen to inflorescences failed to produce any increase in the mean number of seeds per inflorescence, measured for non-barren inflorescences, for either species. However, in B. paludosa, the addition of pollen increased the numbers of inflorescences that set seed from 20% (controls) to 45% (pollen-added treatment). This suggests either unusual patterns of pollen movement among and within plants or control of the pattern of seed-set within a plant. Pollen additions failed to alter seed-set in B. spinulosa. It is possible that a greater abundance of pollinators in the woodland ensures adequate pollination for these plants     

Recognition of Bacterial Initiator tRNA by an Initiation Factor

Initiation factor F2a of E. coli seems to recognize only fMet-tRNA_f. This may be analogous to the recognition of other aminoacyl-tRNAs by elongation factor T.     

Development of Eimeria auburnensis in Cell Cultures

SYNOPSIS. Monolayer established cell line cultures of bovine kidney (Madin-Darby) and human intestine (Intestine 407), as well as embryonic bovine tracheal and embryonic spleen cell line cultures were inoculated with E. auburnensis sporozoites and observed for a maximum of 22 days. Mature 1st generation schizonts developed in the kidney, tracheal and spleen cells. In the intestine cells, trophozoites were seen in 3 of 4 experiments, but schizonts were not found. Sporozoites penetrated cells, beginning within a few minutes after inoculation. Penetration was usually accomplished within 10 seconds, and the body of the sporozoite underwent a slight constriction as it passed thru the host cell membrane. Some sporozoites left cells. Numerous intracellular sporozoites were observed in kidney, tracheal and spleen cultures. Crescent bodies were seen in the parasitophorous vacuole as early as 1 day after inoculation. At this time, the nuclei of most intracellular sporozoites had changed from vesicular to compact. Beginning 4 days after inoculation, enlarged sporozoites and parasites having a sporozoite shape, but with 2-5 nuclei, were frequently seen. These enlarged sporozoites and sporozoite-shaped schizonts evidently transformed into trophozoites and spheroidal schizonts by means of lateral outpocketings. Few trophozoites were seen. More immature schizonts developed in kidney cells than in the other cell types. The numbers of mature schizonts observed in kidney and tracheal cells were similar, but development occurred less consistently in the latter. Few immature and mature schizonts developed in spleen cells. Mature schizonts, first seen 9 days after inoculation, were considerably smaller than those reported from calves. Some motile merozoites were seen; evidently no development beyond these occurred. The nucleus and nucleolus of host cells were enlarged; this enlargement was not as pronounced as in infections in calves. Multiple host cell nuclei were frequently observed. Degenerative changes in the cultured cells and in the parasites usually occurred, beginning 9-17 days after inoculation; these were more pronounced in the spleen cells than in the others.