Variability in Microbiological Data from a Stratified Eutrophic Lake

A survey of a stratified eutrophic lake was undertaken to determine the degree of variability in direct counts of bacteria, electron transport system activity, ATP concentration, chlorophyll a concentration and chemiluminescence, in the water column and the sediment. Heterogeneity in the horizontal and vertical dimension was studied in detail and the scale of variability was compared with within-sample and between-sample errors, and with seasonal fluctuations. Variability was greater in the sediment samples, and the coefficient of variation of samples taken at a single site was often as large as that between sites in a transect across the lake. Although this was not an exhaustive survey, the values provided should allow rough estimates to be made of the number of samples required to achieve a given level of precision in future investigations.     

Delayed in vitro Utilization of Glucose by Leishmania tropica Promastigotes*

Leishmania tropica promastigotes do not utilize glucose provided in the medium until late log phase. Rapid depletion of glucose from the medium, however, occurs during late log and stationary phases. At about the same time, the cells show maximal rates of glucose uptake as well as peak levels of phosphofructokinase and pyruvate kinase activities. The glucose analog, 2-deoxy-D-glucose inhibits glucose transport. Incorporation of this analog in the growth medium results in inhibition of growth. The hexokinase of L. tropica phosphorylates 2-deoxy-D-glucose. Pyruvate kinase is activated by fructose-1, 6-diphosphate and adenosine monophosphate.     

Leakage from Fruit Cells in Water

When disks of apple tissue are placed in water, 90% of theirelectrolytes and soluble carbohydrates leak out in 2–3h, and cells initially intact and able to exclude Evan's Bluebecome coloured by the dye. Molar glycerol and 0.5M potassiumchloride largely protect the cells from these changes. It issuggested that apple cells burst in water, but not in hypertonicmedia. Leakage from the tissues of other soft fruits (grape,tomato, plum, banana, melon) when placed in water is as rapidand extensive as from apple; but leakage is very much slowerfrom tissues such as potato tuber, beetroot, onion bulb, lettuceleaf, and the fruits of marrow and cucumber. Leakage from applefruit tissue becomes more extensive as the apple develops towardsmaturity.     

Cell distribution and surface morphology in petals, androecia and styles of Commelinaceae

Cell distribution and surface morphology in petals, androecia and styles of Commelinaceae. Epidermal cell shape, distribution, surface topography and cuticular morphology in petals, androecia and styles of 10 species in the Commelinaceae are described. Petals of all species possess a basal area of elongated, straight-sided cells and an area of cells with sinuous, anticlinal walls. The degree of convolution of anticlinal wall and the length of cells varies between genera. The surface of cells in Aneilema, Commelina and Cyanotis are micropapillate. In all other genera they are low-domed. Cuticular surfaces of the three genera are smooth, while in the remainder heavily striated. The cells of stamens, staminodes, staminal hairs, and styles are variably elongated and straight-sided, their surfaces convex and cuticle striated. The degree of striation is less pronounced at the base of each organ but becomes more densely arrayed towards the apex. Petal pigments are located in upper epidermal cells in Tradescantia and Thyrsanthemum , in upper and lower epidermises in Dichorisandra and Commelina , and in both epidermises, and mesophyll of Aneilema. In most species pigmentation of androecium and style is similar to petals though often fainter at base and apex. Flavonols in the pigments give rise to spectral polmorphisms visible in longwave UV light. Epidermal adaptations for light capture in petals is compared to that in leaf structure.