Changes in hydraulic conductance of citrus trees following a reduction in wetted soil volume

Abstract The effcct of the transition from fully to partially wetted soil voluine on transpiration rate and hydraulic conductance of mature citrus trees was examined in a 23-year-old, coninicrcial, sprinklerirrigated, Shanio u t i orange orchard. I rriga t i on frequency was determined by the rate of water loss from the soil, a s measured by neutron probes. The hydraulic conductance of tlic tree was coniputed from the rclationship between sap flow i n the trunk and leaf water potential. The diurnal valucs of leaf water potential and sap flow shifted towards lower levels as tlie water stored in the root zone was depleted. In the fully wetted soil volume the tree hydraulic conductance remained constant throughout the irrigation period, from June to Novcniber. However, partial wetting of the soil volume (40%) caused a reduction in the hydraulic conductance of the tree. Tlie decreased hydraulic conductance is attributed to tlie permanent interruption of water transport in part of tlie root system. Tlie rcsults of tlie experiment suggest that despite tlie increase of irrigation frequency, partial wetting intensifies water stress in tlie trees.     

云南松林的生物量研究

本文研究了云南省易门县海拔1600—1700m的云南松中幼龄林分的生物量。云南松林的生物量随林龄的增加而增加。4年生林分的总生物量为9.985吨/公顷,11年生林分为27.874吨/公顷,23年生林分为69.852吨/公顷。乔木层的器官生物量分配比例随林龄而变化。针叶和树皮的分配比例随林龄的增加而迅速下降;干材和根的比例则不断上升,其中以干材增加最快;树枝的分配比例以11年生林分最大,23年生林分次之,4年生林分最小。     

Comparison of the Disruption of Mitosis and Cell Plate Formation in Oat Roots by DCPA, Colchicine and Propham

Holmsen, J. D. and Hess, F. D. 1985. Comparison of the disruptionof mitosis and cell plate formation in oat roots by DCPA, colchicineand propham.—J. exp. Bot. 36: 1504–1513. Concentrationsof DCPA, propham and colchicine were selected to cause from0% to greater than 60% inhibition of oat (Avena sativa L. ‘Victory’)root growth after 24 h exposure. Root growth progressively declinedas concentrations were raised from 1·0 to 5·6mmol m^–3 DCPA, 1·0–5·0 mmol m^–3propham, and 50–500 mmol m^–3 colchicine. In additionto inhibiting root growth each mitotic disrupter caused theroot tips to swell to an extent dependent upon concentration.All three compounds effectively disrupted mitosis at concentrationsthat caused less than maximal root growth inhibition. Mitoticdisruption was manifest as a reduction in the number of normalmitotic figures and an increase in the number of condensed prophase,multipolar and anaphase bridge division figures. The frequencyof each type of division figure was different for each of thethree compounds. DCPA disrupted mitosis more effectively whencompared with propham and colchicine at concentrations whichcaused the same amount of root growth inhibition. Each mitoticdisrupter also induced the formation of aberrant cell walls.DCPA was the most effective at disrupting cell plate formation,whereas colchicine was least effective. These data suggest thatthe mechanism of action of DCPA is distinct from the mechanismof colchicine or propham Key words: Avena sativa L., mitotic disruption, DCPA, colchicine, propham     

Polynucleotide Ligase and φX174 Single Strand Synthesis

A DNA ligase mutant of E. coli when infected with φX174 produces linear single strands which appear in an intracellular pool and in phage particles. The linear single strands, which are infectious in a spheroplast assay, seem to be a normal intermediate in progeny DNA synthesis.     

Interactions of Vesicular Stomatitis Virus Structural Proteins with HeLa Plasma Membranes

THE processes whereby nucleoprotein core particles of certain animal viruses become enveloped by and bud off from host cell membranes can be studied by preparing membrane^1,2 or “sedimentable”³ fractions from infected cells and examining them for the presence of virus proteins. We find that similar experiments designed to monitor assembly of vesicular stoma-titus virus (VSV) at sites along the plasma membranes of HeLa cells are best interpreted after first investigating the possibility that virus proteins adsorb to plasma membranes during cell fractionation and membrane isolation. In this report, we show that at 0° C the membrane protein of VSV, among other virus proteins, adsorbs to plasma membranes isolated from uninfected HeLa cells. With appropriate pulse-chase experiments, however, we are able to demonstrate the progressive association, in vivo, of VSV core protein with plasma membranes of infected HeLa cells.     

INHIBITION OF CATALASE IN MESENCEPHALIC CULTURES BY l-DOPA AND DOPAMINE

Catalase activity in cell cultures of fetal rat mesencephalon was decreased by 42 and 50%, respectively, after exposure to l-3,4-dihydroxyphenylalanine (l-DOPA, 100 μM) or dopamine (100 μM) for 48 h. Catalase activity was also decreased 21% by 10 μM hydroquinone. Ascorbic acid (200 μM), an agent that suppresses the autoxidation of l-DOPA and dopamine, blocked the anti-catalase effect of l-DOPA, but not that of dopamine. Inhibitors of the A and B forms of monoamine oxidase (20 μM clorgyline plus 20 μM pargyline) had no effect on the anti-catalase action of either l-DOPA or dopamine. The latter results suggest that products of the oxidative deamination of dopamine by monoamine oxidase are not involved in the suppression of catalase activity. However, autoxidation reactions of l-DOPA may play a role since ascorbate suppressed the anti-catalase effect of l-DOPA. On the contrary, the basis for the failure of ascorbate to similarly block the anti-catalase effect of dopamine is uncertain. l-DOPA and dopamine (25 μM) also inhibited crystalline catalase in solution after incubation for 1 h at neutral pH (40–50% inhibition). Inhibition was blocked by 0.45 M ethanol, indicating a need for autoxidation and the formation of compound II, which is an enzymatically inactive form of catalase. The ability to model the enzyme inhibition in purely chemical experiments indicates a probable mechanism for loss of enzymatic activity in cell cultures. Inhibition of catalase may contribute to cell damage during incubation of cultures with l-DOPA, dopamine, or other autoxidizable compounds. Copyright © 1996 Elsevier Science Ltd