Elemental composition at different points of the rainwater harvesting system.

Entry of contaminants, such as metals and non-metals, into rainwater harvesting systems can occur directly from rainfall with contributions from collection surfaces, accumulated debris and leachate from storage systems, pipes and taps. Ten rainwater harvesting systems on the east coast of Australia were selected for sampling of roof runoff, storage systems and tap outlets to investigate the variations in rainwater composition as it moved throughout the system, and to identify potential points of contribution to elemental loads. A total of 26 elements were screened at each site. Iron was the only element which was present in significantly higher concentrations in roof runoff samples compared with tank tap samples (P<0.05). At one case study site, results suggested that piping and tap material can contribute to contaminant loads of harvested rainwater. Increased loads of copper were observed in hot tap samples supplied by the rainwater harvesting system via copper piping and a storage hot water system (P<0.05). Similarly, zinc, lead, arsenic, strontium and molybdenum were significantly elevated in samples collected from a polyvinyl chloride pipe sampling point that does not supply household uses, compared with corresponding roof runoff samples (P<0.05). Elemental composition was also found to vary significantly between the tank tap and an internal cold tap at one of the sites investigated, with several elements fluctuating significantly between the two outlets of interest at this site, including potassium, zinc, manganese, barium, copper, vanadium, chromium and arsenic. These results highlighted the variability in the elemental composition of collected rainwater between different study sites and between different sampling points. Atmospheric deposition was not a major contributor to the rainwater contaminant load at the sites tested. Piping materials, however, were shown to contribute significantly to the total elemental load at some locations.

Metabolic effects of static magnetic fields on Streptococcus pyogenes.

This study aimed to develop a simple experimental system utilising bacterial cells to investigate the dose responses resulting from exposures to static magnetic flux densities ranging from 0.05 to 0.5 T on viability, bacterial metabolism and levels of DNA damage in Streptococcus pyogenes. Exposure of S. pyogenes to a field of 0.3 T at 24 degrees C under anaerobic conditions resulted in a significant (P < 0.05) decrease in growth rate, with an increased mean generation time of 199 +/- 6 min compared to the control cells at 165 +/- 6 min (P < 0.05). Conversely, exposure to magnetic fields of 0.5 T significantly accelerated the growth rate at 24 degrees C compared to control cells, with a decreased mean generation time of 147 +/- 4 min (P < 0.05). The patterns of metabolite release from cells incubated in phosphate buffered saline (PBS) at 24 degrees C and exposed to different magnetic flux densities (0.05-0.5 T) were significantly (P < 0.05) altered, compared to non-exposed controls. Concentrations of metabolites, with the exception of aspartic acid (r = 0.44), were not linearly correlated with magnetic flux density, with all other r < 0.20. Instead, "window" effects were observed, with 0.25-0.3 T eliciting the maximal release of the majority of metabolites, suggesting that magnetic fields of these strengths had significant impacts on metabolic homeostasis in S. pyogenes. The exposure of cells to 0.3 T was also found to significantly reduce the yield of 8-hydroxyguanine in extracted DNA compared to controls, suggesting some possible anti-oxidant protection to S. pyogenes at this field strength.

Autosomal phosphogluconic dehydrogenase polymorphism in the cat (Felis catus L.).

Three patterns of 6-phosphogluconic dehydrogenase activity were obtained by starch-gel electrophoresis of blood from domestic cats. Genetic analysis indicates control of these patterns by a pair of alleles at an autosomal locus. Presence of three enzymatically active bands in heterozygotes and of single bands in homozygotes is compatible with at least a dimeric structure for the enzyme.