The removal of phenols from the waste waters of wood preserving plants has always presented problems. The purpose of this paper is to investigate the possibility of employing a biological system to reduce the phenol content of effluent from these plants.

This study dealt with the life history and population dynamics of the pine vole, Microtus pinetorum. In the past there has been a void of ecological material concerning this small mammal in the southwestern region of its range. From November, 1969, through February, 1970, a survey was conducted in Marion County and Harrison County, Texas, to determine the most suitable habitat for an ecological study of Microtus pinetorum. A study was then initiated in March, 1970, and continued through March, 1971, on an undisturbed marsh five miles south of Marshall, Harrison County, Texas.

Observations of decreases in plasma volume, shifts in plasma and lymph protein concentrations, and increases in capillary permeability at high altitude have been reported in the literature by several investigators. This investigation was begun in an attempt to elucidate the possible significance of these phenomena in future space exploration, and because of the lack of knowledge concerning the underlying mechanisms. The purpose of this investigation was to determine the effects of exposure to hypobaric pressures on the capillary permeability to the normal plasma and lymph proteins.

The effects of X-irradiation at dosages of 40 r, 80 r, 160 r, 240 r, 320 r, 400 r, 800 r, 4 Kr, 8 Kr, and 16 Kr on the oxygen uptake of frog brain (Rana pipiens) tissue slices were studied. A membrane-covered oxygen electrode method was used to measure the respiratory rate. Continuous recordings were made before, during, and following X-irradiation in all of the test experiments. X-irradiation was delivered from a G. E. beryllium window X-ray unit at 120 KVP, 5 ma with a 1/4 mm Al filter.

The purpose of this study was to determine the endogenous levels of indole-3-acetic acid throughout the life cycle of Chlorella pyrenoidosa, and to show a correlation between onset of cell division and IAA levels.

The respiratory activity of three aquatic animals selected from different pollution index classifications is examined in the presence of sublethal concentrations of Dibrom, a commonly used, broad-spectrum, organophosphate insecticide.

It was the purpose of this investigation to isolate and characterize the pigments of Mycobacterium rhodochrous by partition behavior, chromatographic data, and absorption spectra. In addition, it was the purpose to determine whether or not the type of pigments found in M. rhodochrous is typical of those found in other mycobacteria.

Lactate dehydrogenase was isolated in pure form from crude extract of the cestode Hymenoleois diminuta by heat treatment and column chromatography. The purified enzyme has a specific activity of 106 units per mg protein. The molecular weight of the purified protein was 75,000 as determined by Sephadex gel filtration and analytical ultracentrifugation. An equilibrium ultracentrifugation study suggests a subunit molecular weight of 39,000. From these data, a dimer form of the native enzyme is proposed.

The objective of this study was to determine the kinds and numbers of food organisms consumed by Corydalus cornutus, and to investigate its periodicity of feeding during the spring months in the Brazos River, Palo Pinto County, Texas. A total of 468 larvae were collected at two-week intervals from February 29 to May 14, 1971. Larvae were taken at opportunity during three periods of the day, 6am.-12pm., 12pm.-6pm., and 6pm.-12am. A total of 23 different food items was observed in the 121 stomachs containing food. An expedient method of dissection of the digestive tract is included.

The purpose of this investigation was to explore how geosmin, an odorous compound produced by certain algae and actinomycetes, may affect the growth of a selected, odor producing actinomycete of the genus Streptomyces.

Malic enzyme from the rat tapeworm, Hymenolepis diminuta, has been purified 320-fold to a final specific activity of 29.4. The purification procedure included heat treatment, followed by column chromatography with Sephadex G-20, two phosphocellulose columns, and Sephadex G-200, respectively. The final purified enzyme appeared to be homogeneous on disc gel electrophoresis and G-200 gel filtration.