Lethal toxicity values (96 h LC50; mg Cd/L) for the test species were similar: Lepomis cyanellus, 11.52; Notropis lutrensis, 6.62; Pimephales promelus, 3.58. However the effects of cadmium concentration and exposure time on temperature tolerance varied between species. Neither cadmium concentration nor exposure time had a significant effect on the CTM of green sunfish. Both cadmium concentration and exposure time had a significant effect on the CTMs of red shiners and fathead minnows. By day 10 mean CTMs were 2.3 t- 4.5 C (red shiners) and 4.2 to 5.7 C (fathead minnows) lower than control CTM. These results suggest a potential problem in cadmium contaminated systems for high environmental temperatures to stress or kill fish.

This study determined effects of addition of secondarily treated municipal wastewater effluent on an urban reservoir receiving system. Monthly water quality monitoring of the receiving reservoir and the wastewater, chemical analysis, and monthly laboratory algal assays, were conducted from September 1984 to September 1985. The nutrient status and algal growth potential of the receiving water and the wastewater confirmed the biostimulatory properties of the wastewater. Field validation studies were conducted using limnocorrals. Tertiary treatment of the wastewater using chemical coagulation precipitation with alum and ferric chloride reduced phosphorus concentrations in the wastewater to levels which supported significantly less algal biomass than untreated wastewater. These studies indicate ferric chloride to be a more effective coagulant for phosphorous removal alum.

The objectives of this research were to identify the form of Azotobacter as it exists in situ in the soil; to compare its resistance to that of laboratory grown cysts typical of those described in the literature; and to compare its resistance to that of cells grown on dialyzed soil agar. In addition, the morphology of the cells grown on dialyzed soil agar was examined by light and electron microscopy and then compared to the cysts grown on n-butanol Burk's medium. Dipicolinic acid and oxygen uptake rate were measured in cysts and on cells grown on dialyzed soil agar in order to determine whether the cells grown on dialyzed soil agar were endospores or other dormant form and also to measure the respiratory quotient in these cells.

The objectives of this project were to develop a high performance liquid chromatographic method for separating the pigment esters mixture, to determine the locations of the pigment moiety in the isolated esters using pholosiphases, and to characterize the pigment-protein complex and determine its distribution in other bacteria. Saponification of the two pigment esters 1 and 2 with aqueous KOH yielded two free pigments on TLC plates developed by two solvent systems. The fasters moving of these two free pigments co-chromatographed with the one free pigment produced from each pigment ester by phospholipase A2 treatment. This suggests that the pigment molecule is a methoxy derivative of xanthomonadin and is esterified to the 2-position of the glycerol moiety of each pigment ester. No free pigment was released from phospholipases C and D treatment of the two pigment esters, indicating that pigment is not esterified to the sorbitol or phosphate moiety of pigment esters 1 or 2.

High Performance Liquid Chromatography (HPLC) has been employed as an analytical tool for the purification and separation of nucleic acids. A Nucleogen DEAE 4000-10 weak anion exchange column, prepacked with modified silica gels, was used to purify and separate a number of Escherichia coli plasmids. Plasmid DNAs were extracted by the alkaline lysis method. The cleared lysate was injected directly onto the Nucleogen column, and the peaks were collected, desalted and analysed by gel electrophoresis. On the chromatogram, the pBR322 formed a distinctive peak at 27 minutes and partial separation was made for the E. coli V517 plasmids. Plasmid pBR322 showed a clear band without any detectable contamination on agarose gel. This purified plasmid DNA is biologically active for enzymatic reaction commonly used in genetic engineering techniques.