Abstract:Stage I Vb sporangiophores of Phycomyces grow into the windthe anemotropic response-and away from gravity-the geotropic response . A procedure has been designed to measure the equilibrium bend angle that results when the two stimuli are given simultaneously over a long period of time . This angle will be referred to as the anemogeotropic equilibrium angle. This measurement of a sensory response is analogous to the photogeotropic equilibrium angle in which the variable stimulus is light instead of wind . We hav… Show more
“…Since the magnitude of wall stress is a function of cell turgor pressure, values for cell turgor and for the factors which control turgor are needed for quantitative models of the mechanics of sporangiophore growth. Moreover, it has been argued that the avoidance and wind responses of Phycomyces are controlled by the concentration of water vapor surrounding the sporangiophore (Gyure et al, 1984).…”
The physical characteristics which govern the water relations of the giant-celled sporangiophore of Phycomyces blakesleeanus were measured with the pressure probe technique and with nanoliter osmometry. These properties are important because they govern water uptake associated with cell growth and because they may influence expansion of the sporangiophore wall. Turgor pressure ranged from 1.1 to 6.6 bars (mean = 4.1 bars), and was the same for stage I and stage IV sporangiophores. Sporangiophore osmotic pressure averaged 11.5 bars. From the difference between cell osmotic pressure and turgor pressure, the average water potential of the sporangiophore was calculated to be about -7.4 bars. When sporangiophores were submerged under water, turgor remained nearly constant. We propose that the low cell turgor pressure is due to solutes in the cell wall solution, i.e., between the cuticle and the plasma membrane. Membrane hydraulic conductivity averaged 4.6 x 10(-6) cm s-1 bar-1, and was significantly greater in stage I sporangiophores than in stage IV sporangiophores. Contrary to previous reports, the sporangiophore is separated from the supporting mycelium by septa which prevent bulk volume flow between the two regions. The presence of a wall compartment between the cuticle and the plasma membrane results in anomalous osmosis during pressure clamp measurements. This behavior arises because of changes in solute concentration as water moves into or out of the wall compartment surrounding the sporangiophore. Theoretical analysis shows how the equations governing transient water flow are altered by the characteristics of the cell wall compartment.
“…Since the magnitude of wall stress is a function of cell turgor pressure, values for cell turgor and for the factors which control turgor are needed for quantitative models of the mechanics of sporangiophore growth. Moreover, it has been argued that the avoidance and wind responses of Phycomyces are controlled by the concentration of water vapor surrounding the sporangiophore (Gyure et al, 1984).…”
The physical characteristics which govern the water relations of the giant-celled sporangiophore of Phycomyces blakesleeanus were measured with the pressure probe technique and with nanoliter osmometry. These properties are important because they govern water uptake associated with cell growth and because they may influence expansion of the sporangiophore wall. Turgor pressure ranged from 1.1 to 6.6 bars (mean = 4.1 bars), and was the same for stage I and stage IV sporangiophores. Sporangiophore osmotic pressure averaged 11.5 bars. From the difference between cell osmotic pressure and turgor pressure, the average water potential of the sporangiophore was calculated to be about -7.4 bars. When sporangiophores were submerged under water, turgor remained nearly constant. We propose that the low cell turgor pressure is due to solutes in the cell wall solution, i.e., between the cuticle and the plasma membrane. Membrane hydraulic conductivity averaged 4.6 x 10(-6) cm s-1 bar-1, and was significantly greater in stage I sporangiophores than in stage IV sporangiophores. Contrary to previous reports, the sporangiophore is separated from the supporting mycelium by septa which prevent bulk volume flow between the two regions. The presence of a wall compartment between the cuticle and the plasma membrane results in anomalous osmosis during pressure clamp measurements. This behavior arises because of changes in solute concentration as water moves into or out of the wall compartment surrounding the sporangiophore. Theoretical analysis shows how the equations governing transient water flow are altered by the characteristics of the cell wall compartment.
“…Interlaced throughout this literature are references to effects of water vapor, long regarded as the avoidance gas by Gamow and his co-workers (e.g., Johnson and Gamow, 1971;Gamow and Bottger, 1982b;Pellegrino et al, 1983;Gyure et al, 1984). As noted above, the idea that sporangiophores avoid water goes back to Wortmann (1881), who obtained different results with wet and dry pasteboard.…”
Section: Effects Of Water Vapormentioning
confidence: 99%
“…Materials that actively absorb water, such as NaOH, KOH, or plaster saturated with CaCl2, did not attract sporangiophores (Elfving, 1916(Elfving, -1917. Attempts to generate growth responses to step-changes in relative humidity have consistently failed (Cohen et al, 1975(Cohen et al, , 1979Gyure et al, 1984). Gyure et al (1984) found that sporangiophores grew more steeply (over periods of several hours) into wet winds then dry winds, but the relevance of this to avoidance is not clear.…”
The sporangiophore of the fungus Phycomyces bends away from nearby objects without ever touching them. It has been thought that these objects act as aerodynamic obstacles that damp random winds, thereby generating asymmetric distributions of a growth-promoting gas emitted by the growth zone. In the interest of testing this hypothesis, we studied avoidance in an environmental chamber in which convection was suppressed by a shallow thermal gradient. We also controlled pressure, temperature, and relative humidity of the air, electrostatic charge, and ambient light. A protocol was established that yielded avoidance rates constant from sporangiophore to sporangiophore to within +/- 10%. We found that avoidance occurred at normal rates in the complete absence of random winds. The rates were smaller at 100% than at lower values of relative humidity, but not by much. Remarkably, at a distance as great as 0.5 mm, avoidance from a 30-micron diam glass fiber (aligned parallel to the sporangiophore) was about the same as that from a planar glass sheet. However, the rate for the fiber fell more rapidly with distance. The rate for the sheet remained nearly constant out to approximately 4 mm. We conclude that avoidance depends either on adsorption by the barrier of a growth-inhibiting substance or emission by the barrier of a growth-promoting substance; it cannot occur by passive reflection. Models that can explain these effects are analyzed in the Appendix.
“…This apparent contradiction might be resolved if it could be shown that a humid wind caused an overall softening of the sporangiophore's cell wall which may have directly enhanced bending. In support of this hypothesis, Gyure et al (5) reported that after several hours of growth in a high humidity wind, the cell wall begins to weaken under the weight of the sporangiophore's head, and the head begins to droop. The data obtained in the present investigation also support the hypothesis that the cell wall becomes softer when exposed to humid wind.…”
mentioning
confidence: 94%
“…Recent studies using a humidified wind tunnel have shown that as the humidity of the wind is increased, the sporangiophore shows a quantitative increase in its equilibrium bend angle (5). This observation argues against Pellegrino's (9, 10) mass transfer model.…”
ABSTRACIThe mechanical extensibilities of stage IVb Phycomyces were measured before and after a humidified wind stimulus. We find that when the humidity of the wind is greater than that of the ambient air, there is an increase in the mechanical extensibility of the cell wall. We also find that a step decrease in wind humidity results in a decrease in the mechanical extensibility of the cell wall.The avoidance response of Phycomyces was first discovered by Elfving (3) in 1881, and in recent years has been well documented (1, 2, 6). The avoidance response occurs when a sporangiophore is placed within several mm of a solid barrier. The response is observed when the sporangiophore grows away from the barrier. This cell wall bending occurs because the portion of the cell wall nearest to the barrier grows faster than the portion farthest away from the barrier. If a sporangiophore is enclosed by a double barrier, a barrier enclosing both sides of the cell, no bending occurs, but a transient increase in total cell wall growth rate is observed; this phenomenon is known as the avoidance growth response (7). Although the precise mechanism of the avoidance response remains unknown, it has been proposed that the cell wall of the sporangiophore softens in response to an avoidance gas that is emitted from the growing zone (4). The presence of the barrier increases the concentration of the gas near the cell wall surface proximal to the barrier. Recent studies indicate that the avoidance gas may be water (4).Cell wall extensibility studies have shown that changes in the growth rate of the Phycomyces sporangiophore are accompanied by changes in the mechanical properties of the cell wall. Ortega et al. (8) reported that transient increases in both cell wall growth rate and cell wall extensibility occur after the cell is given a saturating light stimulus. Similar increases in growth and extensibility were observed during the avoidance growth response (7). These studies suggest that transient increases in cell wall growth rate result from transient increases in cell wall mechanical extensibility.Cohen et al. (2) reported that mature sporangiophores grow into the wind; this behavior is now known as the anemotropic response. Recent studies using a humidified wind tunnel have shown that as the humidity of the wind is increased, the sporangiophore shows a quantitative increase in its equilibrium bend angle (5). This observation argues against Pellegrino's (9, 10) mass transfer model. According to the model, the equilibrium bend angle should be inversely related to the humidity of the wind. Thus, the anemotropic response should be less dramatic in high humidity than in low humidity. This apparent contradiction might be resolved if it could be shown that a humid wind caused an overall softening of the sporangiophore's cell wall which may have directly enhanced bending. In support of this hypothesis, Gyure et al. (5) reported that after several hours of growth in a high humidity wind, the cell wall begins to weaken under the weight of the ...
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