Difference in light-induced increase in ploidy level and cell size between adaxial and abaxial epidermal pavement cells of Phaseolus vulgaris primary leaves

Changes in nuclear DNA content and cell size of adaxial andabaxial epidermal pavement cells were investigated using brightlight-induced leaf expansion of Phaseolus vulgaris plants. Inprimary leaves of bean plants grown under high (sunlight) ormoderate (ML; photon flux density, 163 µmol m^–2s^–1) light, most adaxial epidermal pavement cells hada nucleus with the 4C amount of DNA, whereas most abaxial pavementcells had a 2C nucleus. In contrast, plants grown under lowintensity white light (LL; 15 µmol m^–2 s^–1)for 13 d, when cell proliferation of epidermal pavement cellshad already finished, had a 2C nuclear DNA content in most adaxialpavement cells. When these LL-grown plants were transferredto ML, the increase in irradiance raised the frequency of 4Cnuclei in adaxial but not in abaxial pavement cells within 4d. On the other hand, the size of abaxial pavement cells increasedby 53% within 4 d of transfer to ML and remained unchanged thereafter,whereas adaxial pavement cells continuously enlarged for 12d. This suggests that the increase in adaxial cell size after4 d is supported by the nuclear DNA doubling. The differentresponses between adaxial and abaxial epidermal cells were notinduced by the different light intensity at both surfaces. Itwas shown that adaxial epidermal cells have a different propertythan abaxial ones. Key words: Cell enlargement, endopolyploidization, epidermal pavement cells, incident light intensity, leaf expansion, nuclear DNA content, Phaseolus vulgaris     

Epidermal focussing and effects upon photosynthetic light-harvesting in leaves of Oxalis

Abstract. In Oxalis , epidermal cells on both the adaxial and abaxial surface of the leaf concentrated light within the leaf by a lens mechanism. Focal lengths of epidermal cells were estimated using two methods: they were calculated from radius of curvature measurements taken from individual epidermal cells, and were measured directly in agarose replicas of the leaf surface. In the three species of Oxalis examined, light that was incident upon the adaxial leaf surface was concentrated within the palisade, whereas light that was incident upon the abaxial leaf surface was concentrated within the spongy mesophyll. Using sensiometric analysis, theoretically maximal focal intesifications were measured in leaf replicas at the focal maximum and at intermediate positions corresponding to the mid-region of the palisade and spongy mesophyll tissues. Focal intensifications ranged from 2.2 to 10.4 times incident light at the focal maximum, and 1.3 to 4.5 in the palisade or spongy mesophyll layers. Elimination of epidermal focussing, by covering the leaf surface with a thin layer of mineral oil, strongly affected chlorophyll fluorescence induction curves resulting in a decrease of 10–40% in the initial (F₀) and variable fluorescence (F_v). These results are consistent with the interpretation that the chloroplasts were adapted to their light microenvironment within the leaf and that focussing by the epidermis channelled light to a population of chloroplasts that were adapted to high light.     

Drought effects on cellular and spatial parameters of leaf growth in tall fescue

The effect of drought and recovery on cellular and spatial parametersof the growth process in tall fescue leaves was studied in twoexperiments. In both experiments plants grown on vermiculiteand maintained in a controlled environment were submitted toa 7 d drought period generated by withholding water. Droughtwas followed by a 3 d recovery period in experiment II. As leafelongation rate (LER) decreased during developing drought boththe growth zone length (initially 40 mm) and the maximum relativeelemental growth rate (initially 0.09 mm mm^–1 h^–1during the dark period of diurnal cycles) within the growthzone declined. But the growth zone still exhibited a lengthof approximately 15 mm when LER approached 0 under severe drought(–2.0 MPa predawn leaf water potential). The growth potentialof the basal 15-mm-long portion of the leaf was conserved duringthe period when drought effected the complete arrest of leafelongation. A (retrospective) analysis of the position-timerelationships of epidermal cells identified on leaf replicas(experiment II) indicated that the cell flux out of the growthzone responded very sensitively to drought. Before drought theflux was maximum at approximately 3.2 cells (cell file h)^–1during the dark period. Flux decreased to 0 when leaf elongationstopped. Flux also varied diurnally both under well-wateredand droughted conditions. In well-watered conditions it wasabout 30% less during the light than the dark period. Cell elongationwas also sensitive to drought. Under well-watered conditionsepidermal cell elongation stopped when cells attained a lengthof approximately 480 µm. During developing drought cellsstopped elongating at progressively shorter lengths. When LERhad decreased to almost nil, cells stopped elongating at a lengthof approximately 250 µn. When drought was relieved followinga 2 d complete arrest of leaf elongation then cells shorterthan 250 µm were able to resume expansion. Following rewateringcell flux out of the growth zone increased rapidly to and abovethe pre-drought level, but there was only a slow increase overtime in the length at which cell elongation stopped. About 2d elapsed until the leaf growth zone produced cells of similarlength as before drought (i.e. approximately 480 µm). Key words: Epidermal cell length, cell flux, (leaf) growth zone, leaf elongation rate, relative elemental growth rate, position-time relationships (path line, growth trajectory), drought, water deficit     

Epidermal Cell Division and the Coordination of Leaf and Tiller Development

Initiation and development of grass leaves and tillers are oftendescribed individually with little attention to possible interrelationshipsamong organs. In order to better understand these interrelationships,this research examined epidermal cell division during developmentaltransitions at the apical meristem of tall fescue (Festuca arundinaceaSchreb.). Ten seedlings were harvested each day for a 9-d period,and lengths of main shoot leaves and primary tillers were measured.In addition, numbers and lengths of epidermal cells were determinedfor 0·5 mm segments along the basal 3 mm of each leafand tiller. Primordia development and onset of rapid leaf elongationwere characterized by an increase in the number of cells perepidermal file with mean cell length remaining near 20 µmper cell. After the leaf had lengthened to 1-1·5 mm,cells near the leaf tip ceased dividing and increased in length,at which time leaf elongation rate increased rapidly. Liguleformation, marking the boundary between blade and sheath cells,occurred prior to leaf tip emergence above the whorl of oldersheaths, while the earliest differentiation between blade andsheath cells probably began when leaves were < 1 mm long.Major transitions in leaf and tiller development appeared tobe synchronized among at least three adjacent nodes. At theoldest node, cessation of cell division in the leaf sheath wasaccompanied by initiation of cell division and elongation inthe associated tiller bud. At the next younger node the ligulewas being initiated, while at the youngest node cell divisioncommenced in the leaf primordium, as elongation of a new leafblade began. This synchronization of events suggests a key rolefor the cell division process in regulating leaf and tillerdevelopment.Copyright 1994, 1999 Academic Press Festuca arundinacea Schreb., tall fescue, cell division, leaf initiation, tillering, ligule development     

Light Gradients and the Transverse Distribution of Chlorophyll Fluorescence in Mangrove andCamelliaLeaves

The light gradient and transverse distribution of chlorophyllfluorescence in mangrove andCamellialeaves, which have differentmorphological characteristics, were examined using a micro-fluorescenceimaging system reported previously (Takahashiet al., Plant,Cell and Environment17: 105–110, 1994). Epidermal cellsscattered light strongly, resulting in an increase in the fluencerate in epidermal cells. For theCamellialeaf, a light gradientwas formed by absorption of light by photosynthetic pigmentsassociated with the induction of chlorophyll fluorescence. Forthe mangrove leaf, a light gradient was formed by backward scatteredlight within a thick layer of non-assimilatory cells. Lightwith a low absorption coefficient (515 nm) penetrated deeperthan that with a higher absorption coefficient (477 nm and 488nm) in theCamellialeaf, while light of both wavelengths showedsimilar profiles in the mangrove leaf. In the mangrove leaves,scattered light declined significantly in the non-assimilatorycell layer which is in front of the assimilatory cells. Light,the intensity of which was reduced to approx. 10% of the maximum,was well scattered and induced a considerable amount of chlorophyllfluorescence in the assimilatory cells, which appear to be wellorganized to capture weak light.Copyright 1998 Annals of BotanyCompany fluorescence, intact leaf, light gradient, mangrove (Rhizophora mucronataLamk.),Camellia japonicaL.     

Studies on Foliar Penetration: IX. PATTERNS OF PENETRATION OF 2,4-DICHLOROPHENOXYACETIC ACID INTO THE LEAVES OF DIFFERENT SPECIES

The comparative patterns of penetration of 2,4-dichlorophenoxyaceticacid (2,4-D) into the leaves of Phaseolus vulgaris, Zea mays,Pisum sativum, Beta wlgaris, Helianthus annuus and Gossypiumhirsuium have been examined. Save for Zea and Gossypium where there is little change withthe stage of leaf development the rates of penetration intoboth surfaces decrease as the leaf matures. The relative ratesare dependent on the species and the age of the leaf but thereare differences between the surfaces. In Phaseolus the characteristicsof primary leaves differ from those of trifoliate leaves sinceonly in immature trifoliate leaves is penetration into the adaxialsurface greater. In darkness the rates of penetration over 24 h remain constantor fall but slightly for all species. Light consistently promotespenetration but with Beta there is a lag before entry is acceleratedinto the abaxial surface as has previously been reported foryoung primary leaves of Phaseolus. For the remaining speciesthe courses of penetration in both light and darkness into bothsurfaces follow similar patterns. As the light intensity isincreased entry is enhanced but the limit of response variesbetween species, between surfaces within species, and in trifoliateleaves of Phaseolus with age. For the six species the order of the relative rates of entryis closely similar whether comparisons are made in light ordarkness or between abaxial and adaxial surfaces: viz. Zea >Helianthus > Phaseolus (primary) > Phaseolus (trifoliate)> Pisum = Beta = Gossypium. The observed specific differencesare discussed in relation to variations in leaf structure, theproperties and thickness of the cuticle and the physiologicaland metabolic processes which influence transport within theepidermal tissues after it has passed through the cuticle bydiffusion.     

Function of silica bodies in the epidermal system of rice (Oryza sativa L.): testing the window hypothesis

Silicon has been considered to be important for normal growthand development of the rice plant (Oryza sativa L.). To investigatethe physiological function of deposited silica in rice leaves,the hypothesis that silica bodies in the leaf epidermal systemmight act as a ‘window’ to facilitate the transmissionof light to photosynthetic mesophyll tissue was tested. Thesilica content of leaves increased with supplied silicon andwas closely correlated with the number of silica bodies perunit leaf area in the epidermal system. There was a significantdifference in silica deposition and formation of silica bodiesbetween Si-treated and non-treated leaves; silicon was polymerizedinside the silica cells and bulliform cells of the epidermis,in Si-treated leaves. Although the ‘windows’ wereonly formed in leaves with applied silicon, optical propertiesof leaf transmittance, reflectance and absorptance spectra inSi-treated and non-treated leaves were almost equal. Furthermore,light energy use efficiency and quantum yield of Si-treatedleaves were less than in leaves not containing silica bodies.Thus, silica bodies, at least based on the data, do not functionas windows in rice leaves. Key words: Silicon, window hypothesis, rice, optical property, quantum yield     

Structure and Function of Silica Bodies in the Epidermal System of Grass Shoots

Silica (SiO₂.nH₂O) is deposited in large quantities in the shootsystems of grasses. In the leaf epidermal system, it is incorporatedinto the cell wall matrix, primarily of outer epidermal walls,and within the lumena of some types of epidermal cells. This biogenic silica can be stained specifically with methylred, crystal violet lactone, and silver amine chromate. At theultrastructural level, the silica in lumens of silica cells,bulliform cells and long epidermal cells is made up of rodsabout 2.5 µm in length and 0.4µm in width. Ultimateparticles in the rods range from 1 to 2 nm in diameter. In contrast,silica in the cell wall matrix of trichomes and outer wallsof long epidermal cells is not rod-shaped, but rather, formsroughly spherical masses. Detailed analyses are presented on the frequencies of occurrenceof the different types of epidermal cells that contain silicain the leaves of representative C₃ and C₄ grasses. The C₄ grasseshave higher frequencies of bulliform cell clusters, silica cells,and long epidermal cells, whereas the C₃ grasses have higherfrequencies of trichomes. No correlation was found in the frequencyof occurrence of silica bodies in bulliform cells for C₃ grassesas compared with C₄ grasses. Of all the grasses examined, Coix,Oryza, and Eleusine had the highest densities of such bodies,and some taxa had no silica bodies apparent in their bulliformcells. The idea that silica bodies in bulliform cells and silica cellsmight act as "windows’ and trichomes might function as‘light pipes’ to facilitate light transmission throughthe epidermal system to photosynthetic mesophyll tissue belowwas tested. The experimental data presented do not support eitherof these hypotheses. C₂ and C₄ grasses, biogenic silica, light pipes, window hypothesis, silica staining, silica ultrastructure     

Cellular Structure and Light Absorbtion in Leaves of Frithia pulchra (Mesembryanthemaceae)

In order to quantify the structural differences between celltypes of leaves from a ‘ window’ plant, an ultrastructuralmorphometric analysis was made of the epidermal, window andchlorenchyma tissues of Frithia pulchra. Epidermal cells arethe largest cells found in Frithia leaves and are characterizedby the presence of a thick outer tangential cell wall and numerousvacuolar inclusions. Epidermal tissue has an optical densityof 0.30. The transparent window tissue (i.e. optical density= 0.08) has a uniform ultrastructure throughout the length ofthe leaf. The vacuome comprises aproximately 97 per cent ofthe protoplasmic volume of window cells. Chlorenchyma cellspossess thin cell walls and are surrounded by numerous intercellularspaces. Cells of the apical chlorenchyma tissue possess approximately30 plastids per cell. These chloroplasts have an average individualvolume of 220 µm². Cells of the basal chlorenchyma tissuecontain chloroplasts that are five to six times smaller andmore numerous than those in cells of the apical chlorenchyma.The increased volume of chloroplasts in the apical comparedwith basal chlorenchyma cells (i.e. 31.4 and 20.2 per cent ofthe protoplasm, respectively) is positively correlated withtheir optical densities of 1.46 and 0.97, respectively. Frithia pulchra, stereology, leaf, light absorption, window plant     

Effect of Shade on Leaf and Cell Size and Number of Epidermal Cells in Garlic (Allium sativum)

Garlic cultivars ‘Bangladesh Local’ and ‘Fructidor’were grown under field conditions in the south-east of Englandand subjected to different shading treatments. The effects ofshading on final leaf size were related to cell numbers anddimensions. An increase in light intensity reduced leaf lengthand size of epidermal cells. In the cv. Fructidor, cell lengthwas reduced, but in the cv. Bangladesh Local, both length andwidth of cells were reduced. The stomatal index decreased withincreasing light intensity in both cultivars. Leaf thicknessincreased with light intensity, resulting in corresponding gainsin leaf d. wt per unit area. Data from cv. Fructidor growing in full sunlight indicated thatthe epidermal tissue adjacent to the abaxial leaf surface hada greater number of cells than that next to the adaxial surface,but no significant differences were found in the correspondingcell depths. The size of epidermal cells in both epidermisesdecreased from the base to tip of the leaf due to reductionin cell length and width. The influences of environmental factorson leaf growth in general, and those related to shade, are alsodiscussed. Allium sativum L. cv. Bangladesh Local, Allium sativum L. cv. Fructidor, epidermal cells, garlic, light intensity, shade, stomatal index     

Isolation and Characterization of Photosynthetically Active Cells from Submersed and Floating Leaves of the Aquatic Macrophyte Potamogeton nodosus Poir

Photosynthetically active cells were isolated by enzymic digestionof floating and submersed leaves of the heterophyllous aquaticmacrophyte Potamogeton nodosus Poir. The yields of cells isolatedfrom floating leaves represented approximately 25% of the leafprotein or chlorophyll, while cell yields from submersed leaveswere only 3%. Photosynthetic activity was maximal in cells isolatedfrom submersed leaves 10 to 14 days after germination of thewinterbuds. Floating leaves were induced by treatment of theplants with abscisic acid. Cells from induced floating leavesshowed maximum photo synthetic rates between 9 and 21 days posttreatment.Phosphoglycerate, fructose 1,6-bisphosphate, sulfate and phosphatewere without significant effect on photosynthesis in eithercell type indicating that the cells were substantially intact.Half-saturation of photosynthesis for bicarbonate was at 0.6mM (pH 7.6) for cells from both leaf types, and the maximumrate was greater for cells from floating leaves. The light intensityfor half-saturation of photosynthesis was approximately 95 µEm^–2s^–1 for cells from both leaf types, and the maximumrate was greater for cells from floating leaves. (Received September 19, 1984; Accepted December 6, 1984)     

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     

Changing Responses of Stomata to Abscisic Acid and CO2 as Leaves and Plants Age

Willmer, C. M., Wilson, A. B. and Jones, H. G. 1988. Changingresponses of stomata to abscisic acid and CO₂ as leaves andplants age.—J. exp. Bot. 39: 401–410. Stomatal conductances were measured in ageing leaves of Commelinacommunis L. as plants developed; stomatal responses to CO₂ andabscisic acid (ABA) in epidermal strips of C. communis takenfrom ageing leaves of developing plants and in epidermal stripsfrom the same-aged leaves (the first fully-expanded leaf) ofdeveloping plants were also monitored. Stomatal behaviour wascorrelated with parallel measurements of photosynthesis andleaf ABA concentrations. Stomatal conductance in intact leavesdecreased from a maximum of 0-9 cm s^{– 1} at full leaf expansionto zero about 30 d later when leaves were very senescent. Conductancesdeclined more slowly with age in unshaded leaves. Photosynthesisof leaf slices also declined with age from a maximum at fullleaf expansion until about 30 d later when no O₂ exchange wasdetectable. Exogenously applied ABA (0.1 mol m^{– 3}) didnot affect respiration or photosynthesis. In epidermal stripstaken from ageing leaves the widest stomatal apertures occurredabout 10 d after full leaf expansion (just before floweringbegan) and then decreased with age; this decrease was less dramaticin unshaded leaves. The inhibitory effects of ABA on stomatalopening in epidermal strips decreased as leaves aged and wasgreater in the presence of CO₂ than in its absence. When leaveswere almost fully-senescent stomata were still able to open.At this stage, guard cells remained healthy-looking with greenchloroplasts while mesophyll cells were senescing and theirchloroplasts were yellow. Similar data were obtained for stomatain epidermal strips taken from the same-aged leaves of ageingplants. The inhibitory effects of ABA on stomatal opening alsodecreased with plant age. In ageing leaves both free and conjugated ABA concentrationsremained low before increasing dramatically about 30 d afterfull leaf expansion when senescence was well advanced. Concentrationsof free and conjugated ABA remained similar to each other atall times. It is concluded that the restriction of stomatal movements inintact leaves as the leaves and plants age is due mainly toa fall in photosynthetic capacity of the leaves which affectsintracellular CO₂ levels rather than to an inherent inabilityof the stomata to function normally. Since stomatal aperturein epidermal strips declines with plant and leaf age and stomatabecome less responsive to ABA (while endogenous leaf ABA levelsremain fairly constant until leaf senescence) it is suggestedthat some signal, other than ABA, is transmitted from the leafor other parts of the plant to the stomata and influences theirbehaviour. Key words: Abscisic acid, CO₂, Commelina, leaf age, senescence, stomatal sensitivity     

Studies on Foliar Penetration: 2. THE ROLE OF LIGHT IN DETERMINING THE PENETRATION OF 2,4 DICHLOROPHENOXYACETIC, ACID

A further study has been made of the factors determining thelevel of penetration of 2,4-dichlorophenoxyacetic acid (2,4-D)into leaves. The technique involves the use of leaf disks and2,4-D containing carbon-14 in the carboxyl group. For Phaseolus vulgaris the influence of the pH of the appliedsolution is greater in the light than in the dark. Between 0and 1,000 f.c. at 27° C there is a small increase in therate of penetration into the abaxial surface. Under these conditionsthe rates remain constant up to 56 hours. This linear relationshipholds for concentrations ranging from 100 to 1,000 mg/l, andthe rate of penetration is directly proportional to the concentration.For intensities in excess of 1,000 f.c. the light response ismarkedly different: over the first few hours there is a steadyand relatively slow rate of penetration which is followed bya second phase when the rate is greatly accelerated. This acceleratedrate can be reversed by transferring the disks to darkness,and does not take place at 1° C. Likewise, if excised disksare left for more than one hour in either the light or the darkbefore applying 2,4-D then there is subsequently no phase ofaccelerated penetration. The course of penetration into theadaxial surface exhibits no accelerated rate, and compared tothe abaxial surface the rates are lower. For leaves of Ligustrum ovalifolium, which lack stomata on theadaxial surface, the rates of penetration at 27° C intoboth surfaces remain constant in either light or darkness. Forboth the adaxial and abaxial surfaces, the rate progressivelyincreases from 0 to; 2000 f.c. and there is no phase of acceleratedpenetration. Penetration into the adaxial surface is less. At1° C the rates for both surfaces in either light or darknessare depressed. If disks of Phaseolus are irradiated with ultraviolet light,subsequent penetration is markedly depressed in the light at27° C, but in the dark or at 1° C it is enhanced. On the basis of these findings it is concluded that both physicaland metabolic factors control the rate of penetration of 2,4-DTransport through the cuticle will be dependent on adsorptionand the length of the diffusion paths. Once diffusion gradientshave been established between the surface of the cuticle andthe outer surface of the cytoplasm in the epidermal cells, thesteepness will be dependent on the rates at which 2,4-D is eitherconverted into some metabolite or moved away from the surfaceor into other cells. The relative importance of physical andmetabolic process will be dependent on the permeability andthickness of the cuticle and the level of metabolic activity.The possible role of ectodesmata in determining both the lengthand steepness of the diffusion paths is discussed.     

The Penetration of Solar Radiation through Leaf Canopies of Different Structure

A comparative study has been made of the penetration of solarradiation through leaf canopies of contrasting structure. Forthis purpose experiments were undertaken on (a) Gladiolus withnearly vertical leaves, (b) Raphanus sativus with its rosettehabit, (c) two varieties of Linum usitatissimum, one an unbranchedflax type and the other a multi-stem linseed type, and (d) Agrostemmagithago where the apical leaves are sharply inclined and thebasal leaves disposed in a horizontal plane. Light gradientswere evaluated at different densities and at varying stagesof development by means of probes of silicon cells. Using afilter (cut off point 72-5 µ) simultaneous measurementswere made of the infra-red and ‘visible’ radiation.The distributions of the leaf and stem area through the canopywere recorded so that light interception per unit surface couldbe assessed. The shape of the light gradient between the top and bottom ofthe canopy was sigmoidal for Gladiolus but much less so forthe other species. Attenuation of the infra-red radiation withdepth was markedly smaller. For valid estimates of the extinction coefficient (K) it isessential to include stem areas; that is on theoretical groundshalf the total stem surface. The values of K were low for allspecies and in particular for Gladiolus. The relationship betweenlight attenuation and leaf area was approximately exponential.For Gladiolus it was established that K can decrease with increasingdensity but no changes with depth in the canopy were evident.The implications of these observations in terms of canopy structureare discussed.     

Red and blue light-stimulated proton efflux by epidermal leaf cells of the Argenteum mutant of Pisum sativum

Light stimulates leaf expansion in dicotyledons by increasingapoplastic acidification, cell wall loosening and solute accumulationfor turgor maintenance. Red and blue light enhance growth viadifferent photo-systems, but the cellular location and modesof action of these systems is not known. Here, the effect of red and blue light was studied on transportprocesses in epidermal cells of expanding leaves of the Argenteummutant of Pisum satlvum. Both red and blue light caused extraceiiuiaracidification by isolated epidermal tissue, which was stimulatedby extracellular K⁺ and inhibited by DCCD at 0.1 mol m^–3.Acidification induced by red compared with blue light showeddifferent saturating kinetics in fluence rate-response curves.Under near saturating light conditions the effects of red andblue light were additive. The red light-induced acidificationwas inhibited by far-red light while the blue light-inducedacidification was not. Light caused a hyperpoianzation of themembrane potential in epidermal strips, and stimulated ⁸⁶Rb⁺uptake by epidermal protoplasts. These results show that phytochromeand an additional blue light-photoreceptor function in isolatedepidermal cells to promote proton efflux, hyperpolarization,and cation uptake. Key words: Pisum sativum, light-induced acidification, ion transport, epidermis, photoreceptor     

Comparative Leaf Epidermal Anatomy of Mutants of Barley (Hordeum vulgare L. 'Himalaya') which Differ in Leaf Length

We wished to determine the nature of differences in epidermalcell numbers and dimensions between leaves of different lengthin mutants of barley (Hordeum vulgare L. ‘Himalaya’).Three comparisons were made: leaf one (L1)vs. leaf four (L4);wild typevs. nine dwarf mutants and wild typevs. a slender mutant.L1 was shorter than L4, and for most lines this was associatedwith a change in epidermal cell number for the blade, and inboth cell number and length for the sheath. Compared to wildtype, the smaller leaves of dwarf plants generally had shorterand fewer cells in both blade and sheath. The blade of slenderplants was the same length (L1) or longer (L4) than wild type,while the sheath was longer than that of wild type for bothL1 and L4. Slender plants had longer but fewer cells than thewild type along the blade of L1, and shorter but more cellsfor the blade of L4. In the sheath, slender plants had longerand more (L1) or fewer (L4) cells than did the wild type. ForL1, variation in blade width amongst the barley lines was associatedwith a change in file width and file number. For L4, blade widthvaried only with file number, except for slender plants wherenarrow blades were associated with reduced file width. Hencethere was no consistent correlation between changes in cellsize or cell (or file) number with changes in leaf length orwidth. Differences depended on the leaf (L1vs. L4), leaf part(bladevs. sheath), and the nature of the mutation (dwarfvs.slender). Barley (Hordeum vulgare L. ‘Himalaya’); leaf epidermis; dwarf mutant; slender mutant     

Structure and Function in the Grass Ligule: Optical and Electron Microscopy of the Membranous Ligule of Lolium temulentum L.

Aspects of the structure and ultrastructure of the membranousligule of mature leaves of Lolium temulentum L. are described.In transverse section the ligule was lens-shaped and wedge-shapedin longitudinal section, 6 or 7 cells wide near the base and1 or 2 cells wide at the edges. Two uniseriate epidermes encloseda chlorenchymatous mesophyll tissue of varying thicknesses;both epidermes were continuous with the leaf adaxial epidermis.The cells comprising these three issues all appeared like typicalgrass epidermal long cells; elongate papillate cells were presentat the edges. No stomata, trichomes, intercellular spaces orvascular tissue were found in the ligule. A marked polarizationof ultrastructural complexity existed from the large-vacuolateabaxial epidermis to the ‘densely cytoplasmic’ small-vacuolateadaxial epidermis. Cells of the latter tissue contained numerousmitochondria, hypersecretory dictyosomes and abundant strandsof rough endoplasmic reticulum. Fluorescence microscopy providedevidence for the accumulation of a polysaccharide-containingmaterial within the periplasmic space next to the outer tangentialwall of adaxial epidermal cells. The ligule is considered tobe a highly organized and differentiated leaf organ with a pholosyntheticmesophyll and an adaxial epidermis active in the synthesis ofprotein and polysaccharide. Darnel, fluorescence microscopy, ligule, Lolium temulentum L., Poaceae, ultrastructure     

Physiological disturbances caused by high rhizospheric calcium in the calcifuge Lupinus luteus

A detailed study of the calcifuge Lupinus Iuteus L. (yellowlupin) has been carried out in an attempt to explain its poorperformance in the presence of high concentrations of rhizosphenccalcium. Plants were grown on two different calcium regimes,1 or 15 mol m^– Ca and, after an establishment period,measurements were made of the rate of leaf extension, finallength of the leaflets and the leaf gas exchange. In addition,the distribution of calcium within the leaf tissue was investigated. At 15 mol m^–3 Ca, leaflet length at full expansion wasreduced as a consequence of reduced extension rate and a declinein cell wall extensibility. Transpiration in excised leaves,assayed gravimetrically, was significantly reduced in plantsgrown in high calcium. Similar results were also obtained fromgas exchange measurements. Analysis of A/C, curves indicatedthat in plants grown in high [Ca] there was a substantial reductionin net assimilation over a range of concentrations of CO₂ X-raymicroanalysis revealed that a large amount of cal cium deliveredin the xylem sap is retained in the mesophyll tissue, and mostof that reaching the epidermal tissue is not found in the guardcells but in the cells adjacent to them, which in this speciesare not anatomically distinct as ‘subsidiary’ cells. Key words: Calcium, calcifuge, Lupinus luteus, stomata, leaf growth     

Nitrogen Effects on Leaf Anatomy within the Intercalary Meristems of Tall Fescue Leaf Blades

Longitudinal elongation contributes most to leaf area expansionof grasses and its rate is known to be strongly affected byN. Our objective was to determine the effect of two N regimes(N₀and N+) on the gradient of leaf tissue formation in meristemsof two contrasting tall fescue (Festuca arundinacea Schreb.)genotypes. Proportions of epidermal, mesophyll and vasculartissue as well as intercellular air space were determined throughoutthe base of actively elongating leaves. The area of leaf transversesections nearly doubled between the ligule and the distal endof the growth zone (about 30 mm), and was mainly associatedwith lateral epidermal and mesophyll cell division in the proximal5.0–7.5 mm. Further increase in transverse area was dueto the formation of intercellular airspace and transverse expansionof epidermal cells. Depending on genotype and N treatment themesophyll, epidermis, vascular bundles and air space comprised45–54%, 20–28%, 6–9%, and 17–21%, respectively,of transverse leaf area in the distal part of the growth zone.After a slight increase close to the leaf base, the area ofvascular tissue remained constant throughout the growth zone.The proportion of air space to mesophyll space was higher atN₀than at N+ because mesophyll area was enhanced by N+ to agreater degree than by N₀. In the genotype with slow leaf elongation,the increase in cross-sectional leaf area was due to an increasein both leaf width and leaf thickness. In the genotype whichhad faster leaf elongation and wider leaves, only leaf thicknesswas enhanced by N+. Copyright 2001 Annals of Botany Company Festuca arundinacea(Schreb.), tall fescue, leaf anatomy, growth zone, nitrogen