scholarly journals Theoretical and Experimental Exclusion of Errors in the Determination of the Elasticity and Water Transport Parameters of Plant Cells by the Pressure Probe Technique

1979 ◽  
Vol 64 (1) ◽  
pp. 18-24 ◽  
Author(s):  
Ulrich Zimmermann ◽  
Dieter Hüsken
Keyword(s):  
Water Transport ◽  
Plant Cells ◽  
Pressure Probe ◽  
Transport Parameters ◽  
Probe Technique

Modification of the pressure-probe technique permits controlled intracellular microinjection of fluorescent probes

1991 ◽  
Vol 98 (4) ◽  
pp. 539-544
Author(s):  
K. J. OPARKA ◽  
R. MURPHY ◽  
P. M. DERRICK ◽  
D. A. M. PRIOR ◽  
J. A. C. SMITH
Keyword(s):  
Fluorescent Probes ◽  
Lucifer Yellow ◽  
Turgor Pressure ◽  
Plant Cells ◽  
Pressure Probe ◽  
Simple Modification ◽  
Symplastic Transport ◽  
Probe Technique ◽  
Cell Turgor ◽  
Leaf Trichome

The pressure probe has been widely used to study the water relations of plant cells. Here we describe a simple modification of the pressure-probe technique that permits the controlled microinjection of fluorescent probes into plant cells while simultaneously measuring cell turgor pressure. Using the pressure probe, less than 1 nl of the membrane-impermeant fluorescent dye Lucifer Yellow CH was introduced into micropipettes and subsequently injected into leaf trichome cells of Nicotiana clevelandii. Disruption of cell contents could be minimized by raising the hydrostatic pressure in the probe prior to impalement to a value approaching the anticipated cell turgor pressure. Injections to the cytosol resulted in intercellular symplastic transport of the dye in both acropetal and basipetal directions. In contrast, no symplastic transport was observed following an injection of dye into the vacuole. As measured with the pressure probe, cell turgor pressures were in the range 0.18 to 0.36 MPa; the half-time for water exchange across the cell boundary was approximately 10 s. The potential of this technique for the study of turgor-pressure-dependent intercellular transport and the hydraulic conductivities of the tonoplast, plasmalemma and plasmodesmata is discussed.

Extra-Column Effects in Determination of Rate Parameters by the Chromatographic Method

1996 ◽  
Vol 61 (6) ◽  
pp. 844-855 ◽  
Author(s):  
Olga Šolcová ◽  
Petr Schneider
Keyword(s):  
Chromatographic Method ◽  
Dynamic Method ◽  
Axial Dispersion ◽  
Transport Parameters ◽  
Porous Particles ◽  
Loop Detector ◽  
Single Pellet ◽  
Set Up ◽  
Extra Column Effects

It was shown that the sampling loop, detector and connecting elements in the chromatographic set-up for determination of transport parameters by the dynamic method significantly influence the response peaks from columns packed with porous or nonporous particles. A method, based on the use of convolution theorem, was developed which can take these effects into account. The applicability of this method was demonstrated on the case of axial dispersion in a single-pellet-string column (SPSR) packed with nonporous particles. It is possible to handle also responses from columns packed with porous particles by a similar procedure.

Inhibition of carbon fixation as a function of zinc uptake in natural phytoplankton assemblages

1979 ◽  
Vol 59 (4) ◽  
pp. 937-949 ◽  
Author(s):  
Anthony G. Davies ◽  
Jillian A. Sleep
Keyword(s):  
Carbon Fixation ◽  
Natural Populations ◽  
Plant Cells ◽  
Toxic Metal ◽  
Vitamin B ◽  
Phytoplankton Assemblages ◽  
Metal Contents ◽  
Rate Limiting ◽  
Natural Phytoplankton

There is now a substantial body of evidence that the growth rates of phytoplankton in culture are more closely related to the cellular levels of the rate-limiting constituent, be it a nutrient, micronutrient or toxic metal, than to the concentrations in the supporting medium; nitrate, Caperon (1968); phosphate, Fuhs (1969); silicate, Paasche (1973); vitamin B12, Droop (1968); iron, Davies (1970); mercury, Davies (1974); cadmium, Davies (1978a). This has suggested the requirement for a technique which would allow the determination of comparable relationships for natural populations of phytoplankton - how, for instance, their carbon fixation rates depend upon the metal contents of the plant cells. Although the effects of metals upon carbon fixation in phytoplankton assemblages from several different sea areas have already been examined (Knauer & Martin, 1972; Patin et al. 1974; Zingmark & Miller, 1975; Ibragim & Patin, 1976) no data seem to have been obtained on the levels of the metals present in the phytoplankton at the time of the measurements.

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