Evaluation of a Non-Destructive Method for Measuring Turgor Pressure in Helianthus

The portable instrument described by Heathcote, Etherington,and Woodward (1979) for the non-destructive measurement of turgorpressure was evaluated in Helianthus annuus and Helianthus paradoxus.A good correlation was obtained between turgor pressure measuredwith the instrument and turgor pressure estimated by the pressure-volumetechnique for individual leaves allowed to dry after excision;however, variation in both the intercept and slope of the relationshipoccurred between leaves. Consequently, there was no correlationbetween the output of the instrument for individual leaves andthe turgor pressure of the same leaves estimated by conventionalmethods. Moreover, for a given leaf, the instrument had onlya limited ability to detect temporal variation in turgor pressurewhen compared with turgor pressure calculated from measuredvalues of leaf water potential and leaf osmotic potential. Theinstrument's output was influenced by its proximity to majorveins and by leaf thickness. We conclude that variability inleaf thickness and the presence of large veins limits its usefulnessfor measurement of turgor pressure in Helianthus. Key words: Leaf thickness, Turgormeter, Turgor pressure, Helianthus     

Feline Leukaemia Viral Antigens and Antisera to the Group Specific Antigens of the Murine Leukaemia Viruses

GEERING et al.¹ reported that feline leukaemia viruses shared one of the group specific antigens of the murine leukaemia viruses, gs-3, as detected by immunoprecipitation in agar gels with broadly reactive rat antisera to the group specific antigens of the murine leukaemia viruses (MuLV). Subsequently, they found that this shared group specific antigen was also present in the hamster and rat C-type viruses². Work by Schafer³ and our own immunodiffusion⁴ and complement fixation studies have confirmed the immunological reactivity between the feline leukaemia viral antigens and broad-reacting murine leukaemia group specific antisera. We have now applied this interspecies immunological reaction between the murine and feline C-type viruses to quantitative studies of the feline leukaemia viruses. Broad-reactive murine leukaemia-sarcoma group specific antisera prepared in rats by the induction of murine sarcoma virus (MSV) tumours^{5, 6} were found to be as useful and nearly as sensitive as a feline leukaemia-sarcoma specific, group specific antiserum for the in vitro detection and assay of the noncytopathogenic feline leukaemia virus (FeLV).     

The Effect of Water Stress on the Vegetative Growth of White Clover (Trifolium repens L): Comparison of Long-term Water Deficit and a Short-term Developing Water Stress

White clover plants were subjected to either a short-term developingwater stress or long-term stable levels of water deficit on‘water stress columns’. The short-term stress reducedplant water status to –2?0 MPa over 15 d. The water stresscolumns imposed only mild levels of water stress (a reductionof 0?35 MPa in leaf water potential for the more severe treatment)but these were maintained for several weeks. The absolute growthof plants on the control columns was maintained throughout theexperimental period. Vegetative growth was measured. Stolon, petiole, and laminagrowth were all reduced to some extent when plants were grownsymbiotically. The two regimes gave comparable results. Whennitrate was supplied there was no effect of water stress. Aconsiderably reduced absolute growth rate did not result ina similar decrease in final organ size. Stolon growth was mostreduced by water stress. Leaf death during water stress wasas important as changes in growth in determining final dry matteryield. Consequently, the yield of petiole and lamina from plantsgrown without supplied nitrate on the water stress columns waslower than that of stolon at the end of the treatment period. The merits of the water stress column system for imposing long-termwater deficit are discussed. Key words: Trifolium repens, white clover, water stress, vegetative growth     

Use of the Pressure Chamber in Membrane Damage Studies

The ability to detect membrane damage in plant leaves by thepressure chamber technique was evaluated. Membrane damage wasinduced by freezing and thawing, absorption of the host-specifictoxin victorin, ozonation, inoculation with Helminthosporiummaydis, and spraying with the phytotoxin, fusicoccin. The pressure-volumerelationships, i.e. the volume of sap expressed from a leafwith incremental increases in pressure, were compared in leaveswith intact or damaged membranes. Where membrane damage waswidespread throughout the leaf, sap was expressed at pressuresas low as one tenth of those needed in leaves with intact membranesand at low pressures the amount of water expressed from leaveswith damaged membranes was up to 10 times that from leaves withintact membranes. Further, the pressure-volume curves of healthyleaves became linear when the leaf turgor potential was reducedto zero, but were non-linear in leaves with damaged membranes.Ozone treatment, inoculation with H. maydis, or spraying withfusicoccin damaged only a proportion of the leaf cells, andpressure-volume relationships more nearly resembled those obtainedwith healthy leaves rather than those obtained with freezingand thawing and absorption of victorin. It is concluded that the pressure chamber can be used to observemembrane integrity, but its ability to detect damage may belimited to conditions in which the majority of cells in theleaf are damaged.     

Effects of Pressure Increase and Release on Temperature within a Pressure Chamber Used to Estimate Plant Water Potential

During a water-potential measurement sequence, temperature changewithin the pressure chamber exhibits certain distinct phases.At the introduction of gas into the chamber there is a rapidincrease in temperature, normally in excess of 8 ?C above ambient,which is directly related to the rate of pressure increase.After reaching a maximum, temperature begins to decline graduallyduring continued pressure increase, and subsequently falls toambient after gas entry coases. When pressure is rapidly releasedfrom the chamber at the end of a measurement, temperature instantlyfalls to subzero values. The causes of these temperature changes are explained in termsof simple thermodynamics, and ways of reducing them are described.