The influence of salinity on phosphate uptake and distribution in lupin roots

Treeby, M. T. and van Steveninck, R. F. M. 1988. The influence of salinity on phosphate uptake and distribution in lupin roots. - Physiol. Plant. 72: 617–622.
The uptake and distribution of phosphate in lupin ( Lupinus luteus L. cv. Weiko III) roots under moderate salt (NaCl) stress was studied. Vacuolar inorganic phosphate (PJ concentrations in high phosphate plants were decreased by salt, although whole root P| was unaffected. In low phosphate plants, vacuolar P_i was unaffected by salt while whole root P_i was increased. Phosphate uptake was not altered by salt in high phosphate plants, but was depressed in low phosphate plants. These observations lead to the conclusion that in high phosphate plants P_i accumulates in cytoplasm and/or stele, ultimately giving rise to phosphate toxicity in shoots. Increasing phosphate supply had no effect on Na⁺ accumulation in root cell vacuoles in the epidermis or cortex, but the concentration of Cl⁻ in endodermal vacuoles was lowered.     

The ultrastructure of wheat leaves II. The effects of kinetin and ABA on detached leaves incubated in the light

Summary Incubation of detached wheat leaves in water in the light results in a temporary accumulation of starch in the chloroplasts. This accumulation is prevented by treatment with ABA. On the other hand, treatment of the detached leaves with kinetin causes a large increase in the size and number of starch grains.     

Neural coding of natural stimuli: information at sub-millisecond resolution

Sensory information about the outside world is encoded by neurons in sequences of discrete, identical pulses termed action potentials or spikes. There is persistent controversy about the extent to which the precise timing of these spikes is relevant to the function of the brain. We revisit this issue, using the motion-sensitive neurons of the fly visual system as a test case. Our experimental methods allow us to deliver more nearly natural visual stimuli, comparable to those which flies encounter in free, acrobatic flight. New mathematical methods allow us to draw more reliable conclusions about the information content of neural responses even when the set of possible responses is very large. We find that significant amounts of visual information are represented by details of the spike train at millisecond and sub-millisecond precision, even though the sensory input has a correlation time of ~55 ms; different patterns of spike timing represent distinct motion trajectories, and the absolute timing of spikes points to particular features of these trajectories with high precision. Finally, the efficiency of our entropy estimator makes it possible to uncover features of neural coding relevant for natural visual stimuli: first, the system's information transmission rate varies with natural fluctuations in light intensity, resulting from varying cloud cover, such that marginal increases in information rate thus occur even when the individual photoreceptors are counting on the order of one million photons per second. Secondly, we see that the system exploits the relatively slow dynamics of the stimulus to remove coding redundancy and so generate a more efficient neural code.     

Photodynamic effects of haematoporphyrin derivative on DNA repair in murine L929 fibroblasts.

Illumination with red light of murine L929 fibroblasts that had been sensitized with haematoporphyrin derivative caused DNA single-strand breaks after a lag time of about 20 min, as revealed by alkaline elution. The cells appeared not to be capable of recovering from this damage. The photodynamic effect of haematoporphyrin derivative on DNA repair was assessed by monitoring the repair kinetics of DNA damage induced by either X-rays, u.v. light (254 nm) or methyl methanesulphonate treatment subsequent to a non-DNA-damaging photodynamic treatment with haematoporphyrin derivative. On 'post-incubation', the normally rapid repair of X-ray-induced DNA strand breaks did not occur, whereas with u.v. light and methyl methanesulphonate treatment after photodynamic treatment prolonged post-incubation resulted in an increase in the number of strand breaks rather than the normally observed decrease. This clearly shows that, after a photodynamic treatment with haematoporphyrin derivative that itself did not cause strand breaks, excision repair in L929 cells is severely inhibited at a stage beyond the incision step.     

Phases in the development of riverine plankton: Examples from the rivers Rhine and Meuse

Observations on phyto and zooplankton in two hydrographically different rivers were compared in order to discriminate phases in plankton development. Along the longitudinal axis of the River Rhine a gradual increase in the development of phytoplankton was observed, which reached its maximumca. 100 km before the river flows into its artificial sedimentation area. The development of rotifer populations was slightly retarded as compared with that of phytoplankton and highest population densities were only reached in the sedimentation area. Crustaceans developed in significant numbers, not until the river water had entered the sedimentation area. Development of zooplankton coincided here with a strong decrease in the density of phytoplankton. A similar trend in plankton development was observed in the River Meuse, although in this river the highest densities of phyto and zooplankton already occurred in its middle reaches. The differences in the timing of plankton growth in the two rivers are probably caused by differences in flow regime between both rivers. The River Rhine, which is fed by rainwater and melting of glaciers in the Alps, has a relatively constant discharge. On the other hand, the low discharge of the rain-fed River Meuse combined with an increased residence time of the water as a consequence of large numbers of weirs, allows a full cycle of plankton development long before its discharge into the sea. This phenomenon was also reflected in the silicate cycle in the Meuse, where the consumption by planktonic diatoms and the regeneration of silicate of deposits seem to be important. In contrast, in the main branches of the River Rhine only the effects of silicate consumption were detectable.     

Quantitative Estimates of Phosphorus Concentrations within Lupinus luteus Leaflets by Means of Electron Probe X-ray Microanalysis

Phosphorus contents of epidermal vacuoles and mesophyll cells of Lupinus lutens leaflets were measured by electron probe x-ray microanalysis of fully hydrated, bulk frozen samples. Quantitation was achieved using standard solutions containing colloidal graphite to simulate cell contents and the derived nonlinear relationship between peak over background ratio and concentration improved the accuracy of the analytical procedure. Inorganic phosphate contents of mesophyll cells were shown to be highly dependent on phosphate nutrition. Comparison with data obtained from conventional analysis leads to the suggestion that in heterogeneous tissues the inorganic phosphate concentrations of the cytoplasm may show greater variation than observed in the cytoplasm of simple plant systems such as cell suspension and root tips.     

Determination of the role of polyphosphate in transport-coupled phosphorylation in the yeast Saccharomyces cerevisiae

The role of polyphosphate in 2-deoxy-D-glucose transport was studied in yeast cells, pulse-labeled with [³²P]orthophosphate, by comparing the concentrations and specific activities of polyphosphate, orthophosphate and 2-dGlc-phosphate. When 2-dGlc transport was measured under aerobic conditions, it appeared that polyphosphate replenished the orthophosphate pool, indicating that polyphosphate has, at least mainly, an indirect role in sugar phosphorylation. Also in cells with a reduced respiratory capacity, due to a treatment with antimycin A, no direct role for polyphosphate in 2-dGlc transport could be detected. Under these conditions, only a very limited breakdown of polyphosphate occurred, probably because of the small decrease in the orthophosphate concentration.Abbreviations 2-dGlc 2-deoxy-D-glucose - P_i orthophosphate - P_n polyphosphate - SP sugar phosphate