Bacteria transport and deposition under unsaturated conditions: the role of the matrix grain size and the bacteria surface protein

Unsaturated (80% water saturated) packed column experiments were conducted to investigate the influence of grain size distribution and bacteria surface macromolecules on bacteria (Rhodococcus rhodochrous) transport and deposition mechanisms. Three sizes of silica sands were used in these transport experiments, and their median grain sizes were 607, 567, and 330 microm. The amount of retained bacteria increased with decreasing sand size, and most of the deposited bacteria were found adjacent to the column inlet. The deposition profiles were not consistent with predictions based on classical filtration theory. The experimental data could be accurately characterized using a mathematical model that accounted for first-order attachment, detachment, and time and depth-dependent straining processes. Visual observations of the bacteria deposition as well as mathematical modelling indicated that straining was the dominant mechanism of deposition in these sands (78-99.6% of the deposited bacteria), which may have been enhanced due to the tendency of this bacterium to form aggregates. An additional unsaturated experiment was conducted to better deduce the role of bacteria surface macromolecules on attachment and straining processes. In this case, the bacteria surface was treated using a proteolitic enzyme. This technique was assessed by examining the Fourier-transform infrared spectrum and hydrophobicity of untreated and enzyme treated cells. Both of these analytical procedures demonstrated that this enzymatic treatment removed the surface proteins and/or associated macromolecules. Transport and modelling studies conducted with the enzyme treated bacteria, revealed a decrease in attachment, but that straining was not significantly affected by this treatment.     

Biomechanical model of the P-type ion pumps of the cell

The mechanisms of the Na/K pump and of the primary Ca pumps of the cell have not yet been clarified. A biomechanical model of these so-called p-type ion pumps is proposed here. It is based on the assumption that the Na ⁺ and Ca ²⁺ ions are occluded by a contracting protein chain cooperating with the ATPase section of the pump. After transfer of the chain into the region of high Na ⁺ or Ca ²⁺ concentration, the ions are released through stretching of the chain by the ATPase. In the backward transfer of the chain, a retrograde transport of Na ⁺ ions is prevented through occlusion of K ⁺ ions by another region of the same chain. In the case of Ca ²⁺ ions, a similar effect is expected from hydrated Mg ²⁺ ions. The two sections of the chain discriminate between the electrical field strength at the surface and the polarizability of the ions. The most likely mechanism for the transfer of the ion-binding chain is considered to involve a thermally induced transition of a pump dimer between two almost equivalent stable orientations in the membrane.     

Characteristics of arsenic accumulation by the seaweeds Fucus spiralis and Ascophyllum nodosum

This study examines the accumulation of ⁷⁴As-arsenic in the seaweeds Fucus spiralis (L.) and Ascophyllum nodosum (L.) collected from Restronguet Creek in southwest England during 1978. Also, the influence of environmental factors (valence state of arsenic, pH, salinity, temperature, phosphate concentration) and metabolic inhibitors on the uptake of arsenic by F. spiralis is examined. Most of the arsenic in the seaweeds was non-exchangeable with labelled arsenic in the medium. The accumulation of ⁷⁴As reached a steady state in 1 to 8 d, depending on the species and external arsenic concentration. At steady state the accumulated arsenic is proportional to external arsenate concentration. F. spiralis accumulated 4 times more arsenate than arsenite. The short-term uptake of arsenic increased in proportion to the external arsenic concentration up to a level of 1000 g l^-1; it then remained constant at higher levels of arsenic. Arsenic uptake increased in direct proportion to increasing temperature. Variation of pH or salinity had no effect on arsenic incorporation. The accumulation of arsenic occurred only in living tissue and was inhibited by KCN in a concentration-dependent manner. The uptake of arsenic by F. spiralis in the presence of photo-synthetic inhibitors (DCMU or CMU) or in the dark was greater than in the light controls. Thus, it was concluded that energy is required for arsenic uptake and this is derived from respiration rather than photosynthesis. There was no evidence for a common mechanism of phosphate and arsenate uptake by macroalgae, although high concentrations of phosphate (40 to 400 M) initially inhibited arsenate uptake.     

Nitrogen balance in marine fish larvae: influence of developmental stage and prey density

The utilization and fate of nitrogen in larvae of plaice (Pleuronectes platessa), blenny (Blennius pavo) and herring (Clupea harengus), from the stage of first-feeding to metamorphosis, was examined under laboratory conditions. Rates of ammonia excretion, primary amine defaecation, and growth in terms of protein-nitrogen were monitored throughout larval life. Data were used to calculate daily ration, the coefficient of nitrogen utilization (absorption efficiency), and gross and net growth efficiencies. The developmental pattern of nitrogen balance was similar for plaice and blenny larvae. These species showed increasing growth efficiency (k₁: 55 to 80%) with decreasing weight-specific waste nitrogen losses with age. Absorption efficiencies. were high (83 to 98%) in plaice and blenny larvae, and tended to increase with development in the former species. Ration relative to body weight decreased with growth in both species. Herring larval development, although at a slower rate than blenny and plaice, appeared normal up to 33 d, after which high mortality occurred. Absorption efficiency in this species tended to decline (83 to 43%) with age, until metabolic costs exceeded the absorbed ration and growth ceased. Artemia sp. nauplii proved a suitable food source for the rearing of plaice and blenny larvae, but this diet may have long-term toxicity or deficiency effects on herring. Availability and density of food affected nitrogen balance in the larvae of all three species. Feeding stimulated the output of wastes in excretion and defaecation by a factor of up to ten times the 12-h non-feeding basal rates. Waste nitrogen output reached a peak some 2 to 3 h after commencement of feeding and returned slowly to the baseline in 5 to 10 h after cessation of feeding. There was an asymptotic increase in ration, ammonia output and growth of larvae as prey density increased. Ration saturated at a higher prey density (>4 prey ml^-1) than either growth or excretion rate (1 prey ml^-1). Thus the efficiency with which food is absorbed and utilized for growth must eventually decline in response to high prey density. The idea that larval fish are adapted to maximize ingestion and growth rate, rather than optimize growth efficiency and thus to respond to prey occurring in either low density or in occasional patches, is supported by these results.