An Estimation of the Turgor Pressure Change as One of the Factors of Growth Stress Generation in Cell Walls Diurnal change of tangential strain of inner bark
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Turgor pressure
Strain (injury)
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Immunogold labelling
Tracheid
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Wood samples were taken from the upper and lower sides of 21 naturally tilted trees from 18 families of angiosperms in the tropical rain forest in French Guyana. The measurement of growth stresses ensured that the two samples were taken from wood tissues in a different mechanical state: highly tensile stressed wood on the upper side, called tension wood, and lower tensile stressed wood on the lower side, called opposite wood. Eight species had tension wood fibres with a distinct gelatinous layer (G-layer). The distribution of gelatinous fibres varied from species to species. One of the species, Casearia javitensis (Flacourtiaceae), showed a peculiar multilayered secondary wall in its reaction wood. Comparison between the stress level and the occurrence of the G-layer indicates that the G-layer is not a key factor in the production of high tensile stressed wood.
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Summary This paper describes the effect of light on the diurnal change in the innermost surface of developing secondary walls. Cryptomeria japonica D. Don saplings were grown in two growth chambers, in which temperature and relative humidity were kept constant and the light-dark phase of the photoperiod varied. One chamber reproduced the natural light-dark phase, while the other reversed it. Samples of differentiating xylem were collected during the dark period when the tangential strain, used as an index of volumetric changes in differentiating cells, was high, and during the light period when the tangential strain was low. The innermost surface of developing secondary walls in differentiating tracheids was observed by field emission scanning electron microscopy. In the specimens collected during the dark period, amorphous material was observed and the cell wall surface was immunogold-labeled with an anti-glucomannan antiserum. In the specimens collected during the light period, cellulose microfibrils were clearly evident, and amorphous material and immunogold labeling were rarely observed. These results demonstrate that the diurnal changes in the innermost surface of developing secondary walls correspond to the light-dark cycle over 24 h.
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Summary The tangential strain on the inner bark of Cryptomeria japonica saplings grown in a growth chamber was continuously measured using strain gauges. Compression wood formation was induced by artificial inclination. The diurnal changes in tangential strain during light/dark cycles in the growth chamber differed from those observed in the field. The total strain increased daily, increasing incrementally during dark periods and decreasing in the light, as observed in the field. In the growth chamber, however, steep increases and rapid decreases in strain were found immediately following lights-off and lights-on. In the inclined saplings, the strain increased more on the lower side of the stem than on the upper side; and the increment of the strain in the dark and the decrement in the light were larger on the lower side than on the upper side. The change in tangential strain on the inner bark surface arises from changes in the volume of differentiating cells, corresponding to turgor pressure changes and cell-wall extensibility changes. Therefore, the differentiating tracheids into compression wood appear to expand at night and shrink in the daytime more than the differentiating tracheids into normal wood.
Tracheid
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Turgor pressure
Cryptomeria
Pith
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An instrument containing a linear variable differential transformer was constructed to obtain continuous, nondestructive measurements of both short term changes in stem diameter and long term growth. In cotton plants, stem diameter, leaf water potential, and leaf relative water content are all closely related to net radiation at the top of the canopy. Leaves from the east and west sides of a plant show slight, but consistent differences in diurnal water potential patterns. Stem diameter and leaf water potential are not related by a single-valued function, since there is a diurnal hysteresis between the two, and growth causes an increase in diameter each night. However, the instrument can be used to monitor long term stem diameter growth.
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Turgor pressure
Protoplast
Plant cell
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Strain (injury)
Tension (geology)
Fagus orientalis
Strain gauge
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Microfibril
Secondary cell wall
Elongation
Deposition
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A new method, the turgor clamp, was developed to test the effects of turgor on cell enlargement. The method used a pressure probe to remove or inject cell solution and change the turgor without altering the external environment of the cell walls. After the injections, the cells were permanently at the new turgor and required no further manipulation. Internode cells of Chara corallina grew rapidly with the pressure probe in place when growth was monitored with a position transducer. Growth-induced water potentials were negligible and turgor effects could be studied simply. As turgor was decreased, there was a threshold below which no growth occurred, and only reversible elastic/viscoelastic changes could be seen. Above the threshold, growth was superimposed on the elastic/viscoelastic effects. The rate of growth did not depend on turgor. Instead, the rate was highly dependent on energy metabolism as shown by inhibitors that rapidly abolished growth without changing the turgor. However, turgors could be driven above the maximum normally attainable by the cell, and these caused growth to respond as though plastic deformation of the walls was beginning, but the deformation caused wounding. Growth was inhibited when turgor was changed with osmotica but not inhibited when similar changes were made with the turgor clamp. It was concluded that osmotica caused side effects that could be mistaken for turgor effects. The presence of a turgor threshold indicates that turgor was required for growth. However, because turgor did not control the rate, it appears incorrect to consider the rate to be determined by a turgor-dependent plastic deformation of wall polymers. Instead, above the turgor threshold, the rapid response to energy inhibitors suggests a control by metabolic reactions causing synthesis and/or extension of wall polymers.
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