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K Raschke

Publications and source records attributed to K Raschke.

35 records · Page 2Linked to original sources

Potassium Chloride as Stomatal Osmoticum in Allium cepa L., a Species Devoid of Starch in Guard Cells.

K(+) and Cl(-) contents of guard cells and of ordinary epidermal cells were determined in epidermal samples of Allium cepa L. by electron probe microanalysis; malate contents of the same samples were determined by enzymic oxidation. KCl was, in general, the major osmoticum in guard cells, irrespective of whether stomata had opened on leaves or in epidermal strips floating on solutions. The solute requirement varied between 50 and 110 femtomoles KCl per micrometer increase in aperture per pair of guard cells. Stomata did not open on solutions of K iminodiacetate, presumably because its anion could not be taken up. Stomata opened if KCl or KBr was provided. Taken together, the results indicate that the absence of starch from guard cells deprived them of the ability to produce malate in amounts of osmotic consequence and that the presence of absorbable Cl(-) (or Br(-)) was necessary for stomatal opening.Previous nutrient supply of the plants determined whether the charges of K(+) in guard cells were completely balanced by Cl(-) or only partially. Addition of K(2)SO(4) to the nutrient solution reduced the participation of Cl(-) in stomatal ion transfer, even if epidermal strips of these plants were later exposed to KCl solution. The anion supplying the charge complement in these cases is not known.Although malate appeared not to participate in stomatal ion transfer in onion, epidermal samples of this species did contain malate. Malate accumulated in the epidermis of leaves put into the light but disappeared from illuminated epidermal strips floating on solutions. In whole leaves, epidermal malate content was positively correlated with stomatal opening; in epidermal strips floating on solutions, the correlation was negative or absent.

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Effects of phaseic Acid and dihydrophaseic Acid on stomata and the photosynthetic apparatus.

Plant extracts containing phaseic acid (PA), as well as solutions of purified PA and dihydrophaseic acid (DPA) were applied to leaves, isolated mesophyll cells, and isolated epidermal strips. In Commelina communis, stomatal closure began 4 minutes after the addition of either 20 micromolar (+/-)-abscisic acid or 10 micromolar PA. Stomata closed less rapidly after treatment with 10 micromolar PA than after treatment with 10 micromolar (+/-)-abscisic acid in Amaranthus powelli, Hordeum vulgare, Xanthium strumarium, and Zea mays and did not respond at all to PA in Vicia faba. DPA (10 micromolar) did not cause stomatal closure in any species.Plant extracts containing PA reduced photosynthesis, as reported by Kriedemann et al. (Aust J Plant Physiol 2: 553-567, 1975). Subsequent experiments with PA purified by crystallization and with residues of solvents employed in the extraction of PA proved that it was not PA that impaired photosynthetic O(2) evolution or CO(2) uptake but unidentified contaminants of the allegedly pure solvents.

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Presence of Chloride Reduces Malate Production in Epidermis during Stomatal Opening.

When stomata of isolated epidermis of Vicia faba are allowed to open in the presence of K(+) and iminodiacetate (an impermeant zwitterion), malate is formed in the epidermis; the increases in malate content follow a nearly linear relationship with stomatal aperture. Stomata of leaf sections of V. faba floated on water during opening also exhibit this relationship. When isolated epidermis is offered KCI, this relationship is not observed and less malate is detected at comparable stomatal apertures. The data indicate that Cl(-), if present at concentrations >/= 10(-5) eq liter(-1), can partially satisfy the anion requirement of guard cells of V. faba during stomatal opening. Discrepancies between earlier reports on the relative roles Cl(-) and malate play as counterions for K(+) in guard cells of V. faba could now be explained as resulting from variations in the availability of Cl(-) to guard cells.

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Release of Malate from Epidermal Strips during Stomatal Closure.

Isolated epidermal strips of Vicia faba and Commelina communis release malate into their bathing medium when stomata close. This release was largest (about 0.6 of the initial malate content) when epidermal strips of C. communis were floated on 10(-5) M (+/-)-abscisic acid.

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On the Resistance to Transpiration of the Sites of Evaporation within the Leaf.

The rates of transpiration from the upper and lower surfaces of leaves of Gossypium hirsutum, Xanthium strumarium, and Zea mays were compared with the rates at which helium diffused across those leaves. There was no evidence for effects of CO(2) concentration or rate of evaporation on the resistance to water loss from the evaporating surface ("resistance of the mesophyll wall to transpiration") and no evidence for any significant wall resistance in turgid tissues. The possible existence of a wall resistance was also tested in leaves of Commelina communis and Tulipa gesneriana whose epidermis could be easily peeled. Only when an epidermis was removed from a leaf, evaporation from the mesophyll tissue declined. We conclude that under conditions relevant to studies of stomatal behavior, the water vapor pressure at the sites of evaporation is equal to the saturation vapor pressure.

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Availability of Chloride Affects the Balance between Potassium Chloride and Potassium Malate in Guard Cells of Vicia faba L.

Electron probe microanalysis for K and Cl and enzymic determination of malate were performed on epidermal strips of Vicia faba L. which had been incubated with 0.1 equivalent of K(+) per liter in the absence or presence of Cl(-). In the absence of Cl(-), iminodiacetate, a presumed impermeant zwitterion, served as anion. With no Cl(-) in the medium, 91% of the K(+) imported into the guard cells during stomatal opening was neutralized by malate production; import of Cl(-) (presumably from the rest of the epidermal tissue) contributed 6%. In the presence of Cl(-), 50% of the necessary negative charges were provided by malate synthesis, 45% by Cl(-) import. Stomatal opening was not obviously affected by the chloride concentration in the incubation medium, but malate production declined roughly linearly with the logarithm of [Cl(-)] between 10(-5) and 10(-1) equivalent per liter.

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Gain of the feedback loop involving carbon dioxide and stomata: theory and measurement.

The physiological and physical components of the feedback loop involving intercellular CO(2) concentration (c(i)) and stomata are identified. The loop gain (G) is a measure of the degree of homeostasis in a negative feedback loop [the expression 1/(1-G) represents the fraction to which feedback reduces a perturbance]. Estimates are given for the effects of G on responses of stomata and c(i) to changes in ambient CO(2) concentration, light intensity, and perturbations in the water relations of a leaf. At normal ambient CO(2) concentration, the gain of the loop involving stomatal conductance and c(i) was found to be -2.2 in field-grown Zea mays, -3.6 if plants of this species were grown in a growth chamber, and zero in well watered Xanthium strumarium in the vegetative state.

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Effect of abscisic Acid on the gain of the feedback loop involving carbon dioxide and stomata.

Gains of the feedback loops involving intercellular CO(2) concentration on one hand, and CO(2) assimilation and stomata on the other (= assimilation loop with gain [G(A)] and conductance loop with gain [G(g)]) were determined in detached leaves of Amaranthus powelli S. Wats., Avena sativa L., Gossypium hirsutum L., Xanthium strumarium L., and Zea mays in the absence and presence of 10(-5)m (+/-) abscisic acid (ABA) in the transpiration stream. Determinations were made for an ambient CO(2) concentration of 300 microliters per liter. In the absence of ABA, stomata were insensitive to CO(2) (G(g) between 0.00 and -0.02) in A. sativa, G. hirsutum, and X. strumarium, sensitive in A powelli (G(g) = -0.46), and very sensitive in Z. mays (G(g) = -3.6). Addition of ABA increased the absolute values of the gain of the conductance loop in A. powelli (G(g) = -2.0), G. hirsutum (G(g) = -0.31), and X. strumarium (G(g) = -1.14). Stomata closed completely in A. sativa. In Z. mays, G(g) decreased after application of ABA to a value of -0.86, but stomatal sensitivity to CO(2) increased for intercellular CO(2) concentrations < 100 microliters per liter. The gain of the assimilation loop increased after application of ABA in all cases, from values between 0.0 (A. powelli) and -0.21 (Z. mays) in the absence of ABA to values between -0.19 (A. powelli) and -0.43 (Z. mays) in the presence of ABA. In none of the species examined did ABA affect the photosynthetic capacity of the leaves.The application of ABA caused stomatal narrowing which affected transpiration more than the assimilation of CO(2). In the case of A. powelli the transpiration ratio decreased without a concomitant reduction of the assimilation rate.

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Abscisic Acid Content and Stomatal Sensitivity to CO(2) in Leaves of Xanthium strumarium L. after Pretreatments in Warm and Cold Growth Chambers.

The degree of stomatal sensitivity to CO(2) was positively correlated with the content of abscisic acid of leaves of Xanthium strumarium grown in a greenhouse and then transferred for 24 hours or more to a cold (5/10 C, night/day) or a warm growth chamber (20/23 C). This correlation did not exist in plants kept in the greehouse continuously (high abscisic acid, no CO(2) sensitivity), nor in plants transferred from the cold to the warm chamber (low abscisic acid, high CO(2) sensitivity). The abscisic acid content of leaves was correlated with water content only within narrow limits, if at all. At equal water contents, prechilled leaves contained more abscisic acid than leaves of plants pretreated in the warm chamber. There appear to be at least two compartments for abscisic acid in the leaf.

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Abscisic Acid Content, Transpiration, and Stomatal Conductance As Related to Leaf Age in Plants of Xanthium strumarium L.

Among the four uppermost leaves of greenhouse-grown plants of Xanthium strumarium L. the content of abscisic acid per unit fresh or dry weight was highest in the youngest leaf and decreased gradually with increasing age of the leaves. Expressed per leaf, the second youngest leaf was richest in ABA; the amount of ABA per leaf declined only slightly as the leaves expanded. Transpiration and stomatal conductance were negatively correlated with the ABA concentration in the leaves; the youngest leaf lost the least amount of water. This correlation was always very good if the youngest leaf was compared with the older leaves but not always good among the older leaves. Since stomatal sensitivity to exogenous (+/-)-ABA was the same in leaves of all four age groups ABA may be in at least two compartments in the leaf, one of which is isolated from the guard cells.The ability to synthesize ABA in response to wilting or chilling was strongly expressed in young leaves and declined with leaf age. There was no difference between leaves in their content of the metabolites of ABA, phaseic, and dihydrophaseic acid, expressed per unit weight.

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Prechilling of Xanthium strumarium L. Reduces Net Photosynthesis and, Independently, Stomatal Conductance, While Sensitizing the Stomata to CO(2).

Greenhouse-grown plants of Xanthium strumarium L. were exposed in a growth cabinet to 10 C during days and 5 C during nights for periods of up to 120 hours. Subsequently, CO(2) exchange, transpiration, and leaf temperature were measured on attached leaves and in leaf sections at 25 or 30 C, 19 C dew point of the air, 61 milliwatts per square centimeter irradiance, and CO(2) concentrations between 0 and 1000 microliters per liter ambient air. Net photosynthesis and stomatal conductance decreased and dark respiration increased with increasing duration of prechilling. The reduction in net photosynthesis was not a consequence of decreased stomatal conductance because the intercellular CO(2) concentration in prechilled leaves was equal to or greater than that in greenhouse-grown controls. The intercellular CO(2) concentration at which one-half maximum net photosynthesis occurred remained the same in prechilled leaves and controls (175 to 190 microliters per liter). Stomata of the control plants responded to changes in the CO(2) concentration of the air only slightly. Prechilling for 24 hours or more sensitized stomata to CO(2); they responded to changes in CO(2) concentration in the range from 100 to 1000 microliters per liter.

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Saturation Kinetics of the Velocity of Stomatal Closing in Response to CO(2).

Stomatal closing movements in response to changes from CO(2)-free to CO(2)-containing air were recorded in leaf sections of Zea mays using air flow porometers. The response to CO(2) was fast; the shortest lag between the application of 300 microliters CO(2) per liter of air and the beginning of a stomatal response was 3 seconds. The velocity of stomatal closing increased with CO(2) concentration and approached its maximal value between 10(3) and 10(4) microliters CO(2) per liter of air. The CO(2) concentration at which the closing velocity reached half its maximal value was approximately 200 microliters CO(2) per liter of air, both in the light and in darkness. This indicates that the mechanism of stomatal responses to CO(2) is the same in both light regimes and that the range of stomatal sensitivity to changes in CO(2) concentration coincides with the range of CO(2) concentrations known to occur in the intercellular spaces of illuminated leaves.

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Stomatal opening quantitatively related to potassium transport: evidence from electron probe analysis.

When stomata of Vicia faba opened (from a stomatal aperture of about 2 micrometers to one of 12 micrometers) the solute content of the guard cells increased by 4.8 x 10(-12) osmoles per stoma. During the same time an average of 4.0 x 10(-12) gram equivalents of K(+) were transported into each pair of guard cells. This amount of K(+), if associated with dibasic anions, is sufficient to produce the changes in guard cell volume and osmotic pressure associated with stomatal opening. Analysis of Cl, P, and S showed that these elements were not transported in significant amounts during stomatal opening. This finding suggests that the anions balancing K(+) were predominantly organic. K(+) was specifically required because no other elements, likely to be present as cations, were found to accumulate in appreciable quantities in guard cells of open stomata.

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Stomatal Responses to Pressure Changes and Interruptions in the Water Supply of Detached Leaves of Zea mays L.

Stomata of Zea mays L. respond to changes in hydrostatic pressure in the water supply of the leaves almost instantaneously and in all leaf parts simultaneously. Therefore, the leaf is a hydraulic unit. The stomata are part of it and their aperture is controlled by the water potential in the water-conducting system. Stomatal aperture is not uniquely related to the relative water content of a leaf. The relation depends also on the humidity in the air and is different for the upper and the lower epidermis.

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Temperature and transpiration resistances of xanthium leaves as affected by air temperature, humidity, and wind speed.

Transpiration and temperatures of single, attached leaves of Xanthium strumarium L. were measured in high intensity white light (1.2 calories per square centimeter per minute on a surface normal to the radiation), with abundant water supply, at wind speeds of 90, 225, and 450 centimeters per second, and during exposure to moist and dry air. Partitioning of absorbed radiation between transpiration and convection was determined, and transpiration resistances were computed.Leaf resistances decreased with increasing temperature (down to a minimum of 0.36 seconds per centimeter). Silicone rubber replicas of leaf surfaces proved that the decrease was due to increased stomatal apertures. At constant air temperature, leaf resistances were higher in dry than in moist air with the result that transpiration varied less than would have been predicted on the basis of the water-vapor pressure difference between leaf and air.The dependence of stomatal conductance on temperature and moisture content of the air caused the following effects. At air temperatures below 35 C, average leaf temperatures were above air temperature by an amount dependent on wind velocity; increasing wind diminished transpiration. At air temperatures above 35 C, leaf temperatures were below air temperatures, and increasing wind markedly increased transpiration. Leaf temperatures equaled air temperature near 35 C at all wind speeds and in moist as well as in dry air.

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