The Flux and Distribution of Xylem Sap Calcium to Adaxial and Abaxial Epidermal Tissue 8

Inherent differences in the responses of stomata on abaxialand adaxial epidermal surfaces of leaves of Commelina communishave previously been suggested to be due to differences in theconcentrations of apoplastic Ca. Adaxial stomata have also beenreported to be more sensitive than abaxial stomata to appliedabscisic acid (ABA). The aims of these experiments were to determinethe validity of these conclusions and to see if xylem sap Cahas a role in determining the response of stomata to ABA. It can be shown from measurements of relative stomatal resistance(determined with a viscous flow porometer) and stomatal conductancethat stomata were more open in plants grown on 8-0 mol m^–3Ca, than with those grown on 2-0 mol m^–3 Ca. When attachedleaves were fed with ABA via the transpiration stream neitherthe extent nor the rate with which conductance declined wasdependent on Ca nutrition. The extent of Ca accumulation within both epidermes was relatedto the concentration of Ca in the rhizosphere and in the xylemsap. It did not, however, appear to reflect the apparent differencesin the flux of the transpiration stream between the two epidermes.Plants growing at the lower Ca concentration accumulated proportionallymore epidermal Ca relative to Ca in xylem sap. The evidencepresented suggests that Ca movement from the xylem to the epidermiscannot be simply described by a mass flow model, and that thedistribution of Ca is not an adequate explanation of the differencesin the behaviour of adaxial and abaxial stomata. The potentialrole for changes in xylem sap Ca to act as a regulator of stomatalbehaviour are discussed. Key words: Abscisic acid, calcium, Commelina communis L., stomatal conductance     

In situ Observations of Stomatal Movements

Kappen, L., Andresen, G. and L?sch, R. 1987. In situ observationsof stomatal movements.—J. exp. Bot. 38: 126–141. A device is described by which stomatal movements in situ canbe observed and recorded continuously in light and in darkness.It is mounted in a conditioned CO₂ exchange measuring chamberso that stomatal movements can be observed whilst CO₂ exchange(photosynthesis and respiration) of the same leaf is measured.Advantages and limitations are discussed. By this method itwas shown that stomata of Vicia faba although responding inthe same direction to environmental stimuli exhibited a widerange of pore widths. Responses to changes of air humidity andof CO₂ content were clearly evident when the leaves were exposedto light. Before stomata closed due to decreasing water vapourpressure differences between leaf and air they showed a markedwidening of the pore. An inverse response occurred when watervapour pressure deficit decreased. In darkness stomata did notrespond to such changes. Key words: Stomata, leaf gas exchange, microscopic observation     

Experimental Studies of the Factors Controlling Transpiration: I. APPARATUS AND EXPERIMENTAL TECHNIQUE

Apparatus and experimental techniques are discussed for usein the investigation of transpiration rate of leaves as controlledby stomatal aperture and leaf water content. The leaf chambers used and the methods adopted for the estimationof the water transpired are described. The designs of the porometer cups used for the different typesof leaves (Pelargonium and wheat) employed in the work are described.To obviate the difficulty that stomata within the cup behaveabnormally, the design employed makes possible a removal ofthe cup from the leaf except during the short periods requiredto estimate stomatal resistance to air flow at intervals duringthe course of an experiment. In these experiments the water content of the leaf is changedat will by interrupting the water-supply and re-establishingit to permit recovery from wilting. The methods used to carryout this cycle of operations are fully dealt with. Determinationsof the transpiration and absorption rates during the experimentand of the final leaf water content make it possible to followchanges in leaf water content throughout the experiment. An account is given of the methods used for varying the speedof flow, the humidity, and the CO₂ concentration of the airstreams.     

The Diffusive Conductivity of the Stomata of Wheat Leaves

A leaf chamber (described in detail) was used alternately witha resistance porometer to measure resistance to viscous flowof air through the leaf, and with a diffusion porometer to measurethe differential diffusive flow of hydrogen and air (V_H–V_A)through the leaf and the component of hydrogen flow (V'_H) movingstraight across the leaf. The resistance of the mesophyll isneeded for interpretation: estimates by three different methodsfor viscous flow did not agree very well, but two differentmethods for diffusive flow gave good agreement. For wheat leaves,only very large errors are important. Formal analysis is in three appendixes: I. Interpretation ofviscous and diffusive flow in small pores involves some problemsin molecular physics, complicated by the particular geometryof the wheat stoma. With some uncertainty, formal expressionsare derived for the viscous resistance of a single stoma, rv,and for the resistances to diffusion of hydrogen and air, andof water vapour and carbon dioxide, all expressed as r_s persquare centimetre of leaf surface. The analysis for hydrogen/airis the most uncertain; that for water vapour and carbon dioxideis more reliable. II. An indication is given of the flow characteristicsof the leaf-chamber system, from which rv can be derived, andof the basis for estimating mesophyll resistance. III. The methodof converting estimates of r_s into estimates of V_H–V_Aand V'_H is given. The results presented are expressed as nearly as possible interms of the quantities which were measured. For five leavesthe dependence of V_H–V_A on V'_H agrees well with theoreticalpredictions; the dependence of V_H–V_A (and V'_H) on rv,on average, agrees well with prediction, but involves the assumptionthat the stomata get shorter as they close. The agreement isgood enough to suggest that the formal expressions for r_s interms of stomatal dimensions and molecular gas constants arereliable enough to be carried forward into future transpirationand assimilation studies. The minimum value of ra for watervapour (c. 3 sec cm⁺¹) is close to values found elsewhere bydifferent techniques. At very small stomatal openings there was a large deviationfrom predicted behaviour, such as would occur if the imposedexcess air pressure further closed the stomata during viscousflow experiments.     

The Differential Transpiration Porometer

The construction and testing of a new differential transpirationporometer for stomatal measurements are described. The principleinvolved is explained, and the mathematical theory is dealtwith in an appendix. As a result of experiments comparing the new instrument's readingswith those obtained with a Wheatstone bridge porometer, a relationbetween diffusive conductance and viscous flow conductance isfound; in the case of wheat stomata this approaches a cubicrelation and in the case of Talinum triangulare a quadraticone.     

Control of the Co2 Responses of Stomata by Indol-3ylacetic Acid and Abscisic Acid

Previous studies of stomatal behaviour on detached epidermisof Commelina communis L. have suggested that abscisic acid (ABA)and C02 act independently to cause stomatal closure. Evidenceis presented here that if indol-3ylacetic acid (IAA) is addedto the medium used for incubating the epidermis, an interactionbetween ABA and Co₂ becomes apparent. Increasing concentrationsof IAA reduce the ability of the stomata to respond to CO₂,and ABA appears to antagonize this effect. Recognition of therole of IAA enables us to reconcile earlier conflicting reportsconcerning the interdependence of effects of ABA and Co₂on stomata.     

A surrogate measure of stomatal aperture

It is proposed that a measurement of the peristomatal groove distance (PGD) of guard cells on surface impressions of leaf epidermis can act as a surrogate measure of stomatal aperture. To test this idea, investigations were carried out on two species, one in which it is possible to make direct measurements of pore width with relative ease (Commelina communis L.) and one whose stomata are so small that this is difficult (Phaseolus vulgaris L.). Leaf water vapour conductance measurements were first taken with a porometer, then, without delay, a silicone rubber impression of the leaf was made of the area directly under the porometer cup. From a positive replica of this impression, stomatal aperture, PGD and pore length were measured. The correlations between stomatal aperture and PGD and between PGD and stomatal conductance were positive and highly significant. Because a causal relationship between stomatal aperture and PGD is expected, linear regression was used to obtain equations for converting PGD measurements into estimates of stomatal aperture. These account for 91.7% of the variation of aperture in the case of C. communis and 70.7% in P. vulgaris, suggesting that PGD measurements have potential as an alternative measure of pore width in cases where direct measurements would be both difficult and subject to excessive measurement error or bias.     

Tentoxin Suppresses Stomatal Opening by Inhibiting Photophosphorylation

Tentoxin and, to a lesser extent, dihydrotentoxin (both at 10mmol m^–3) reduce stomatal opening in epidermal stripsof Commelina communis in the light but not in darkness. Thiseffect was significantly greater in normal air than in CO₂-freeair. Fusicoccin overcame the tentoxin effect. However, tentoxindid not inhibit stomatal opening in the light in epidermal stripsof Paphiopedilum harrisianum, a species which lacks guard cellchloroplasts. It is concluded that tentoxin exerts its actionon stomata not by an ionophorous effect in the plasmalemma ofguard cells but by the inhibition of photophosphorylation intheir chloroplasts. The effects of DCMU and tentoxin on guardcells are discussed in terms of their effects on chloroplastsand the extent to which energy is supplied from this organelleduring stomatal opening in the light. The results indicate thatneither photophosphorylation nor non-cyclic electron transportin guard cell chloroplasts are essential for stomatal opening. Key words: Commelina, epidermal strips, Paphiopedilum, photophosphorylation, stomata, tentoxin     

Separation of Direct and Indirect Responses of Stomata to Light: Results from a Leaf Inversion Experiment at Constant Intercellular CO2 Molar Fraction

Previous work has shown that stomata respond directly to light,but it was not clear whether the only additional response isthrough CO₂, or whether some other metabolite is involved inthis response. Gas exchange experiments were done with normallypositioned and inverted leaves of Hedera helix to investigatethis problem. The macroscopic optical properties of the leavesand their anatomical structure were also studied. These experimentssnowed that there is no need to postulate the existence of amessenger other than CO₂ to explain the indirect response ofstomata to light. The experiments also showed that leaf inversionaffects both stomatal conductance and photosynthesis, and highlightthe difficulties involved in the interpretation of the effectof leaf inversion on stomata when stomatal conductance measurementsare not done concurrently with measurements of CO₂ flux densityand intercellular CO₂ molar fraction Key words: Hedera helix, ivy, gas exchange, leaf inversion, stomatal conductance, light, CO₂ flux density, photosynthesis     

Effect of Elevated CO2 on Stomatal Size and Distribution in Perennial Ryegrass

Plants of ryegrass (Lolium perenne L. cv. Melle) were grownfrom the early seedling stage in growth cabinets at a day/nighttemperature of 20/15 °C, with a 12-h photoperiod, and aCO₂ concentration of either 340 or 680 ± 15 µl1^–1 CO₂. Young, fully-expanded, acclimated leaves fromprimary branches were sampled for length of stomata, and ofepidermal cells between stomata, numbers of stomata and epidermalcells per unit length of stomatal row, numbers of stomatal rowsacross the leaf and numbers of stomatal rows between adjacentvein ridges. Elevated CO₂ had no significant effect on any ofthe measured parameters. Elevated CO₂, Lolium perenne, ryegrass, stomatal distribution, stomatal size     

Some Differences in the Responses of Stomata of the Two Leaf Surfaces in Cotton

Some differences in the responses of the upper and lower stomatain cotton (Gossypium hirsutuni) are presented. These differenceswere observed in the course of some studies in which the transpirationof the two leaf surfaces was measured under controlled environmentconditions and the transpiration data used as an estimate ofstomatal response. In darkness the upper stomata were more or less effectivelyclosed while the lower stomata were partially open. Upon illuminationof the leaf with non-saturation or saturation radiation theupper stomata were slower to open than the lower stomata. Thereductions in stomatal aperture which occurs with the increasein age of leaves commenced earlier in the upper stomata andproceeded at a faster rate than the lower stomata. Sudden exposureto saturation radiation caused the stomata of the two leaf surfacesto oscillate. These oscillations were not observed in youngleaves but in older leaves. During ageing of leaves oscillationsof the upper stomata commenced earlier than oscillations ofthe lower stomata. When the petiole was excised in darknessor light the upper stomata showed a transient increase but notthe lower stomata. Gossypium hirsutum, stomatal responses, transpiration     

Calcium Inhibits Ion-Stimulated Stomatal Opening in Epidermal Strips of Commelina communis L.

Inoue, H. and Katoh, Y. 1987. Calcium inhibitsion-stimulatedstomatal opening in epidermal strips of Commelina communis L.—J.exp. Bot. 38: 142–149. Ca²⁺ suppressed both the ion-stimulated stomatal opening andH⁺ extrusion of pre-illuminated epidermal strips isolated fromCommelina communis L. In the absence of Ca²⁺, the rate of H⁺release was 18 nmol H⁺ cm^–2 h^–1 per epidermal stripunit area in 150 mol m^–3 KCL at pH 7?4. Half-maximum inhibitionof stomatal opening was observed with 220 mmol m^–3 ofCa²⁺. The hexavalent dye, ruthenium red, showed concentration-dependentprevention of the inhibition by Ca²⁺ of the ion-stimulated stomatalopening. The effect of ruthenium red was non-competitive, andthe K₁ for the calcium inhibition was found to be 3?6 mmol m^–3.The calcium inhibition of H⁺ extrusion was also prevented byruthenium red. These results suggest that Ca²⁺ inhibits theactivity of electrogenic H⁺ translocating ATPase of the guardcell plasma membrane and leads to the suppression of stomatalopening. Key words: Calcium, Commelina communis, ruthenium red, stomata     

Nitric oxide, stomatal closure, and abiotic stress

Various data indicate that nitric oxide (NO) is an endogenoussignal in plants that mediates responses to several stimuli.Experimental evidence in support of such signalling roles forNO has been obtained via the application of NO, usually in theform of NO donors, via the measurement of endogenous NO, andthrough the manipulation of endogenous NO content by chemicaland genetic means. Stomatal closure, initiated by abscisic acid(ABA), is effected through a complex symphony of intracellularsignalling in which NO appears to be one component. ExogenousNO induces stomatal closure, ABA triggers NO generation, removalof NO by scavengers inhibits stomatal closure in response toABA, and ABA-induced stomatal closure is reduced in mutantsthat are impaired in NO generation. The data indicate that ABA-inducedguard cell NO generation requires both nitric oxide synthase-likeactivity and, in Arabidopsis, the NIA1 isoform of nitrate reductase(NR). NO stimulates mitogen-activated protein kinase (MAPK)activity and cGMP production. Both these NO-stimulated eventsare required for ABA-induced stomatal closure. ABA also stimulatesthe generation of H₂O₂ in guard cells, and pharmacological andgenetic data demonstrate that NO accumulation in these cellsis dependent on such production. Recent data have extended thismodel to maize mesophyll cells where the induction of antioxidantdefences by water stress and ABA required the generation ofH₂O₂ and NO and the activation of a MAPK. Published data suggestthat drought and salinity induce NO generation which activatescellular processes that afford some protection against the oxidativestress associated with these conditions. Exogenous NO can alsoprotect cells against oxidative stress. Thus, the data suggestan emerging model of stress responses in which ABA has severalameliorative functions. These include the rapid induction ofstomatal closure to reduce transpirational water loss and theactivation of antioxidant defences to combat oxidative stress.These are two processes that both involve NO as a key signallingintermediate. Key words: Abscisic acid, antioxidants, guard cells, hydrogen peroxide, nitric oxide, oxidative stress, stomata, water stress Received 19 June 2007; Revised 21 September 2007 Accepted 5 November 2007     

Stomata and Structure of Tetraploid Apple Leaves cultured in Vitro

Leaves of anther-derived tetraploid apple (Malus pumila Mill.)shoots were examined by low-temperature scanning electron microscopy(LT-SEM). Leaves were serrate and wide with an undulating adaxialsurface due to convex epidermal cells, apparently without crystallineepicuticular wax. Stomata were absent from the adaxial surface,except for the marginal teeth which exhibited 40-60 stomataper leaf; they probably originated from residual mitotic activity.One third of abaxial stomata was occluded by the residual cuticleof the mother guard cell across the stomatal pore which rupturedwhen the stomata became functional. The stomatal index was 7·2(± 1·6) with 60-75 stomata mm^-2, i.e. abaxialstomata of tetraploid leaves expanded in vitro were less frequentthan those in triploid leaves either cultured in vitro (475-575stomata mm^-2) or grown on the tree (320-390 stomata mm^-2) wherethe stomatal index was 21 (± 4). Freeze-fracture transsectionsshowed that the tetraploid in vitro leaves were composed ofa layer of adaxial epidermal cells, followed by a single layerof palisade cells and four to five layers of spongy mesophyllcells and the abaxial layer of epidermal cells, in contrastto juvenile seedling-grown apple leaves in which the two layersof palisade cells comprised the majority (52-60%) of the leafvolume. The same morphological features, such as wide and lesspointed leaves, reduced stomatal density and stomatal index,and increased stomatal size that were previously reported fortree-grown tetraploid leaves were also expressed in vitro. Thus,causes of the stomatal deformation in tissue-cultured Rosaceaeare interpreted to be in part genetic and not purely environmental.Copyright1994, 1999 Academic Press Malus pumila Mill., apple, biotechnology, breeding, cryo-preservation, CO₂, juvenile, low temperature-scanning electron microscopy (LT-SEM), micropropagation, ploidy, stomata, tissue-culture, transpiration     

Circadian Rhythm of Stomatal Movements in Epidermal Strips

Measurements were made of changes in stomatal pore widths inepidermal strips of leaves ofVicia faba and Commelina communis.Strips were incubated in dilute KCI solutions (1 and 10 molm^–3) flowing through a perfusion chamber on the stageof a microscope and kept for 4 d in continuous light. Circadianrhythms of stomatal apertures were detected in both species.Although the amplitude was small it was statistically significant.It is concluded that at least partof the mechanism for the stomatalrhythm resides in the epidermis, probably in the guard cells. Key words: Cireadian rhythm, epidermal strips, stomata     

A Krypton Diffusion Porometer for the Direct Field Measurement of Stomatal Resistance

A stomatal diffusion porometer is described which measures directlythe diffusion of radioactive krypton through amphistomatousleaves. The porometer is relatively small and portable and iseasily used under field conditions. It consists of a miniaturediffusion chamber above an acrylic plastic reservoir which contains1200 cm³ of air enriched with ⁸⁵Kr. Geiger tubes in the diffusionchamber and in the reservoir monitor the relative concentrationsof 85Kr. Krypton is allowed to diffuse from the larger reservoirthrough the leaf into the diffusion chamber and the time forits concentration in relation to that in the reservoir to changebetween two fixed values is recorded. When this time lapse wascalibrated against known resistances a linear relationship,independent of temperature was found. Sources of error are analysedand some experiments are described in which the porometer wasused to measure diurnal changes in stomatal resistance. Resistancesof potted sunflower plants (Helianthus annuus L.) grown in agreenhouse were measured with both the krypton diffusion porometerand a condensation-type porometer and the results were usedto calculate both cuticular and stomatal resistances. Demonstrationof field measurements with the porometer include data from eucalyptustrees {Eucalyptus camaldulensis Dehn) and from an unirrigatedcotton crop {Gossypium hirsutum var. SJ 2) growing under semi-aridconditions. Stomatal conductance of the cotton crop during theopening phase was linearly related to solar radiation.     

Direct Observation of Reversible and Irreversible Stomatal Responses of Attached Sunflower Leaves to SO(2)

The effects of SO₂ on stomatal aperture of attached sunflower leaves were observed with a remote-control light microscope system that permitted continuous observation of stomatal responses over periods of several hours. The relationship between actual stomatal aperture and stomatal conductance, measured with a porometer, also was examined on leaves before and after exposure to SO₂.

A distinction between uninjured and injured regions was clearly visible on leaves after exposure to 1.5 microliters per liter SO₂ for less than an hour. During the exposure, the mean value of apertures for many stomata, which indicates stomatal conductance and transpiration rate, tended to decrease simultaneously in the uninjured and injured regions. However, the rate of decrease in the injured region was slower than that in the uninjured region because of a transient opening induced by water-soaking in the injured region. The transient opening was less common in stomata near veins and veinlets.

There was a good correlation between pore width and stomatal conductance measured with a porometer before exposure to SO₂. This correlation continued in leaves exposed to SO₂ until visible, irreversible injury occurred, but then it disappeared.

The results of these experiments indicate the necessity of continuous observation of individual stomata under the microscope to understand the effects of air pollutants such as SO₂ on stomatal behavior.

     

Measurement of Stomatal Aperture by Digital Image Processing

We developed a new digital image processing technique for exactlymeasuring the degree of stomatal opening, that is, the ratioof the width to the maximum length of a stomatal pore, and thepore area. We applied this technique to evaluate responses toSO₂ of neighboring stomata in a small region of an intact attachedleaf, with the following results:

1. The pore region could be exactly extracted even when the originaldigital image was of poor quality. The standard errors in theevaluation of the pore area, the pore length, and the pore widthwere 10 µm², 0.3 µm and 0.3 µm, respectively.
2. A wide variety of responses to SO₂ was found among neighboringstomata in a small region of an attached leaf. The differenceswere especially remarkable before water-soaking and wilting.When these began, k₁ showed a local maximum value, and thenall the stomata began to close. These results suggest that stomatalresponses of intact growing plants to air pollutants shouldbe examined from the standpoint of not only the average movementof many stomata but also the movement of each stoma and thatthe interrelationship among movements of neighboring stomatashould be investigated to clarify the mechanism of stomatalresponses to air pollutants.

(Received June 4, 1984; Accepted August 23, 1984)     

An Investigation into the Stomatal Behaviour of a Wilty Mutant of Pisum sativum

The water relations and stomatal behaviour of a wilty line ofpea (JI 1069) were investigated and compared with those of severalnon-wilty lines (JI 1180, JI 1194, and JI 74). The leaves ofthe wilty line were found to have a lower percent water content,water potential and diffusive resistance and the dimensionsof the stomatal cells were larger than those of the non-wiltytypes. The aperture of stomata on epidermal samples taken from plantsin the light or dark period of a diurnal rhythm was consistentlylarger for the wilty pea than for the non-wilty lines, however,their stomatal responses on detached epidermis to light, CO₂and KC1 concentration were similar. There was no differencein response to ABA of stomata on detached epidermis of wiltyor non-wilty types of pea. Key words: Pisum sativum, Wilty mutant, Water relations, Stomatal behaviour     

Stomatal Responses and the Senescence of Leaves

Guard cell responses were examined in green and senescing leavesof Victa faba using detached epidermal strips to eliminate influencesfrom the mesophyll. Stomatal opening was greater in epidermalstrips from mature leaves than from senescing leaves althoughthe latter still retained the ability to respond to CO₂ andto kinetin. It was concluded that the decline in stomatal activityduring senescence is an independent but parallel process tochanges occurring in the mesophyll. Vicia faba, leaf senescence, stomata, kinetin