Frequency distribution of coliforms in water distribution systems.

Nine small water distribution systems were sampled intensively to determine the patterns of dispersion of coliforms. The frequency distributions of confirmed coliform counts were compatible with either the negative-binomial or the lognormal distribution. They were not compatible with either the Poisson or Poisson-plus-added zeroes distribution. The implications of the use of the lognormal distributional model were further evaluated because of its previous use in water quality studies. The geometric means from 14 data sets ranged from 10(-6) to 0.2 coliforms per 100 ml, and the geometric standard deviations were between 10 and 100, with one exception. If the lognormal model is representative of the coliform distribution; the arithmetic mean sample count is a poor estimator of the true mean coliform density, and the probability of water in a distribution system containing small patches with large coliform densities without detection by routine monitoring is finite. These conclusions have direct bearing on the interpretation of microbiological quality standards for drinking water.     

Betaine distribution in Angiosperms

Over 140 Angiosperm species, included in 45 of the 62 orders listed by Engler, have been investigated for the presence of betaines, which were detected in 86% of the species examined and in 43 of the orders. Moreover, betaines were reported earlier in a further seven of the orders. Thus, it can be concluded that betaines are very widely distributed in Angiosperms. The most commonly detected betaines in the study were glycinebetaine and trigonelline, although others, such as prolinebetaine, trans-4-hydroxyprolinebetaine and pipecolatebetaine were found, although with a very restricted distribution. In the large majority of species tested, betaine levels were low (below 0.1%, dry weight).     

Tissue distribution of L-fucokinase in rodents

L-fucose (fucose) is a monosaccharide normally present in mammals and is unique in being the only levorotatory sugar that can be synthesized and utilized by mammals. The metabolism of fucose is incompletely understood, but fucose can be synthesized de novo or salvaged. The utilization of fucose in the salvage pathway begins with phosphorylation by fucokinase. As part of an investigation of fucose metabolism in normal and disease states, we began an investigation of this enzyme. In this report, we present the tissue distribution of the enzyme in rat and mouse. The highest amount of activity was present in brain of both species. Some activity was found in all tissues examined (liver, kidney, heart, lung, spleen, brain, muscle, thymus, white adipose, testes, eye, aorta, small intestine, and submaxillary gland). Very low levels were found in small intestine. Varying levels in the tissues seems most likely to be the result of varying amounts of fucokinase protein as no difference in the Km values of crude enzyme could be shown. Protein-bound fucose levels were determined using the L-cysteine-phenol-sulfuric acid (CPS) assay. There is not a good correlation between fucokinase activity and protein-bound fucose, suggesting some tissues are more active in synthesis of fucose than others.     

The distribution of potassium in plants

Summary Recalculation of some literature data on potassium contents of plants revealed that potassium, like chloride, should be reported on a rational basis such as normality or percentage in plant sap. This would remove the necessity to explain large apparent differences in composition between adjacent plant parts. Potassium closely resembles chloride in its manner of distribution within the plant.     

Subcellular distribution of ascorbate in plants

The compartment specific distribution of ascorbate in plants is of great importance for plant development, growth and defense as this multifunctional metabolite plays important roles in the detoxification of reactive oxygen species (ROS), redox signaling, modulation of gene expression and is important for the regulation of enzymatic activities. Even though changes in ascorbate contents during plant growth and various stress conditions are well documented and the roles of ascorbate in plant defense during abiotic stress conditions are well established, still too little is known about its compartment specific roles during plant development and defense. This mini-review focuses on the subcellular distribution of ascorbate in plants and describes different methods that are currently used to study its compartment specific distribution. Finally, it will also briefly discuss data available on compartment specific changes of ascorbate during some abiotic stress conditions such as high light conditions and exposure to ozone.Key words: ascorbate, mitochondria, chloroplasts, electron microscopy, ozone, high light stress, reactive oxygen speciesAscorbate is one of the most important antioxidants in plants and animals. It detoxifies reactive oxygen species (ROS) either directly or through the glutathione-ascorbate cycle (Fig. 1) and is involved in redox signaling, modulation of gene expression and the regulation of enzymatic activities (extensively reviewed in ref. ¹ and ²). Ascorbate occurs in a reduced form (ascorbic acid) and two oxidized forms (mono- and dehydroascorbic acid). The ratio between reduced and oxidized ascorbate is essential for the ability of the plant to fight oxidative stress. During environmental stress situations when ROS are formed inside the cell, large amounts of dehydroascorbic acid can be formed by oxidation of ascorbic acid which shifts the ascorbate pool more towards the oxidative state and diminishes the antioxidative capacity of the plant. Additionally, environmental stress situations can change total ascorbate contents in plants which makes ascorbate an important stress marker during abiotic and biotic stress situations.^3–11 Ascorbate contents are typically measured biochemically in individual plant organs or tissues and the obtained values represent a combination of the ascorbate status of all individual organelles. As many environmental stress conditions induce highly compartment specific stress responses changes of ascorbate contents in individual organelles might not be detected when ascorbate is measured in whole organs or tissues. This is crucial as data obtained about the antioxidative status from individual organs are often used to interpret the stress response of the whole plant to the exposed stress conditions. Thus, in order to gain a deeper insight into the defense response of plants it is essential to measure changes in the subcellular distribution of these components during environmental stress situations.Open in a separate windowFigure 1Ascorbate-glutathione cycle in plants. Hydrogen peroxide (H₂O₂) within the plant cell can be detoxified by ascorbate peroxidase (APX). In this reaction the reduced form of ascorbate (Asc) is oxidized to monodehydroascorbate (MDHA). MDHA is then either reduced by monodehydroascorbate reductase (MDHAR) to Asc or, since very unstable, reacts to dehydroascorbate (DHA). DHA is reduced by dehydroascorbate reductase (DHAR) to Asc. In this reaction the reduced form of glutathione (GSH) is oxidized to glutathione disulfide (GSSG). GSSG is then reduced by glutathione reductase (GR) to GSH. The electron acceptor NADP is regenerated during the reduction of MDHA and GSSG by the respective enzymes. Asc and GSH are additional able to detoxify reactive oxygen species by direct chemical interaction. Thus, besides the total ascorbate level their redox state (reduced vs. oxidized state) which depends on the activity of the described enzymes (grey boxes) is also very important for successful plant protection.     

The distribution of iridoids in Bignoniaceae

The distribution of iridoids among the tribes of Bignoniaceae is shown. In the present work, 18 species from the tribes Bignonieae and Tecomeae as well as one from Eccremocarpeae have been investigated. These data combined with those obtained through a literature review were analysed and showed that iridoids occur predominantly in the tribe Tecomeae. In this tribe, a chemical distintion between the genera Tabebuia and Tecoma was observed: The iridoids in Tabebuia are decarboxylated whereas in Tecoma they are C-4 formylated. The species from Bignonieae are poorly investigated and only few reports have been published, however, the iridoids found are mainly C-4 carboxylated. The only exception, Dolichandra cynanchoides (=Macfadyena cynanchoides), with decarboxylated iridoids, is also morphologically abnormal in Bignonieae.     

Solute distribution in Suaeda maritima

The distribution of sodium, potassium and glycinebetaine in shoot tissues of salt-treated Suaeda maritima was examined by semi-micro techniques after extraction into toluene-water. Much higher K/Na ratios were observed in the apical regions and in axillary buds than in more mature, fully vacuolated tissues. The younger tissues also contained very high levels of glycinebetaine. Electron-probe X-ray microanalysis of bulkfrozen and fractured preparations showed higher K/Na ratios and higher levels of sulphur and phosphorus in the cytoplasm of leaf primordial cells than in vacuoles of either young or old leaves, although the total counts were higher in the vacuolar samples. The results are discussed in relation to current models of subcellular solute compartmentation and salt tolerance in the Chenopodiaceae.     

Nuclear distribution in Alternaria tenuis

Nuclear distribution and behaviour during vegetative growth and spore formation inAlternaria tenuis was studied utilising the HCl — Giemsa staining technique. The vegetative mycelium and conidia are predominantly monokaryotic. Anastomoses, followed by nuclear migrations, have been recorded. Intercellular nuclear migrations have only been observed in germinating conidia. Nuclear behaviour during conidial formation indicates that the conidia are homokaryotic. Cytological differences have been found in different monocoidal isolates of A. tenuis.     

Nitrate distribution in tropical soils

Summary The downward movement of the nitrate ion in the top 5 ft of Tippera clay loam was followed by applying sodium nitrate at the rate of 2000 pounds per acre to bare fallow soil after different rain intervals during the 1957/58 wet season. At the end of the season soil samples were collected at 6-inch intervals and compared with samples from adjacent plots that received an equivalent anion quantity of sodium chloride after the same rain intervals. After 23.7 inches of rain the distribution of nitrate and chloride anions the soil profile was nearly identical and it was concluded that the anions are equally mobile in this soil.The mean movement of the anion was 1.075 inches for each inch of rainfall. A high positive correlation of 0.946 was obtained between mean movement and rainfall. The downward movement of both anions out of the topsoil appeared to be enhanced by channels left by partly decomposed roots.Application of sodium chloride on sandier soils revealed a much higher mean movement of anions on Blain sand than on Tippera clay loam after equal amounts of rain, but on Florina sand with a high silt content in the topsoil the mean anion movement approached that of the clay soil. The difference is explained in terms of low infiltration rate into the Florina soil.The practical implications of leaching of nitrate in Tippera soil are briefly discussed.     

Three-dimensional stress distribution in arteries

A three-dimensional stress-strain relationship derived from a strain energy function of the exponential form is proposed for the arterial wall. The material constants are identified from experimental data on rabbit arteries subjected to inflation and longitudinal stretch in the physiological range. The objectives are: 1) to show that such a procedure is feasible and practical, and 2) to call attention to the very large variations in stresses and strains across the vessel wall under the assumptions that the tissue is incompressible and stress-free when all external load is removed.     

Load distribution in native cellulose

The properties of cellulose materials are dependent on interactions between and within the cellulose chains. To investigate the deformation behavior of cellulose and its relation to molecular straining, sheets with fibers oriented preferably in one direction were studied by dynamic FT-IR spectroscopy. Celluloses with different origins (spruce pulp, Cladophora cellulose, cotton linters) were used. The sheets were stretched sinusoidally at low strains and small amplitudes while being irradiated with polarized infrared radiation. The cellulose fibers showed mainly an elastic response. The cellulose fibers showed mainly an elastic response. The glucose rings and the C-O-C bridges connecting adjacent rings, as well as the O(3)H.O(5) intramolecular hydrogen bonds are the components mainly deformed under stress, whereas the O(2)H.O(6) intramolecular hydrogen bonds play a minor role. The load distribution was also found to be different in the different allomorphic forms of cellulose I, namely, I(alpha) and I(beta).