Free-space marker studies on the leaf ofZea mays L.

Summary Two free-space marker procedures (Prussian blue and lanthanum nitrate) were employed to determine the pathway(s) followed by water and solutes in the transpiration stream after their introduction into the xylem of small and intermediate bundles, and the effectiveness of the suberin lamellae of the bundle-sheath cells as a barrier to the movement of tracer ions (Fe³⁺ and La³⁺). Judged from the distribution of Prussian-blue crystals (insoluble, crystalline deposits resulting from the precipitation of ferric ions by ferrocyanide anions) and lanthanum deposits, water and the tracer ions moved readily from the lumina of the vessels into the apoplast (cell wall continuum) of the phloem and bundle-sheath cells via portions of vessel primary walls not bearing lignified secondary wall thickenings. Prussian blue and lanthanum deposits were abundant on the bundlesheath cell side of the bundle sheath/mesophyll interface but few occurred on that of the mesophyll, indicating that the suberin lamella is an effective barrier to apoplastic movement of both ferric and lanthanum ions. The presence of Prussian-blue crystals and lanthanum deposits in the compound middle lamella of the radial wall of the bundle-sheath cells indicates that the compound middle lamella provides an apoplastic pathway for transpirational water from the xylem to the evaporating surfaces of the mesophyll and epidermal cells.     

Water Movement Into and Through Tradescantia virginiana (L.) Leaves: II. LIQUID FLOW PATHWAYS AND EVAPORATIVE SITES

Excised leaves of T. virginiana were supplied at their baseswith water containing a dilute solution of lead-EDTA chelate.After the leaf had been allowed to transpire for 3–5 hthe lead was precipitated in situ using hydrogen sulphide. Leafsections were examined microscopically and the path of the transpirationstream and the sites of evaporation inferred from the distributionof lead precipitate. From the distribution of precipitate itwas concluded that there is more evaporation from cells liningthe substomatal cavity, compared with cells in the bulk of themesophyll, than was previously thought to be the case.     

Effect of Phosphorus Nutrition on the Cellular Distribution of Acid Phosphatase in the Leaves of Lycopersicon esculentum L.

A histochemical study using light microscopy has been made ofthe distribution of acid phosphatase (EC 3.1.3.2 [EC] ) activity intransverse sections of fully expanded leaves of Lycopersiconesculentum grown in phosphate-deficient or sufficient media.Leaf tissues were prepared by two methods and were embeddedin paraffin wax. The location of acid phosphatase activity inleaf sections was determined by trapping orthophosphate releasedfrom p-nitrophenyl phosphate with lead acetate and subsequentlyconverting the lead phosphate to optically dense lead sulphide.In leaf sections from control tissue lead sulphide depositswere larpely confined to the spongy mesophyll cells. Whereasthe staining of the palisade cells was limited and of a granularnature, the staining of the spongy mesophyll cells was heavierand coincident with the outline of the individual cells. Moreover,the minor veins were more heavily stained than the surroundingmesophyll cells. Sections of phosphorus-deficient tissues wereheavily stained in both the palisade and spongy mesophyll layersand heavy deposits of lead sulphide were present in the regionsof the minor veins. It is suggested that the enhanced acid phosphataseactivity of the mesophyll cells in fully expanded leaves couldbe involved in the remobilization of phosphate within phosphorus-deficientplants, or be part of a phosphate transporting system, concentratingthe intracellular phosphate from the limiting supply in thesolution bathing the mesophyll cells. Lycopersicon esculentum L., tomato, acid phosphatase, phosphorus nutrition     

Anatomy of Ethylene-induced Petal Abscission in Pelargonium x hortorum

When viewed under the light microscope, the abscission zoneat the petal base of Pelargonium x hortorum consisted of smallcells which, when stained with Toluidine Blue, possessed denselystained cells walls. After treatment with 1 µl l^-1 ethyleneat 22°C, the force required to separate the petals fromthe receptacle declined after a lag phase of only 30 min, withseparation complete 60-90 min later depending upon the stageof development of the flower. Transmission electron micrographsof the petal abscission zones showed evidence of cell wall degradation,particularly in the middle lamella. These cells also containedextensive rough endoplasmic reticulum and numerous Golgi bodiesribosomes. When abscission was complete, cells at the fractureface showed evidence of breakdown of cellular compartmentalization,often with little sign of an intact tonoplast. Scanning electronmicrographs of recently-abscissed surfaces showed that the epidermalcells surrounding the abscisson zone were turgid and rounded,whereas those of the mesophyll cells were partially collapsed.The micrographic evidence is consistent with the hypothesisthat ethylene-induced separation is caused by rapid enzymaticof the cell walls.Copyright 1993, 1999 Academic Press Abscission, cell walls, ethylene, flower, Pelargonium x hortorum     

Scanning Electron Microscopy of Silica Deposits in the Culms, Floral Bracts and Awns of Barley (Hordeum sativum Jess.)

Deposits of silica in the culm internodes, floral bracts andawns of Hordeum sativum Jess (cv Deba Abed) have been investigatedusing the scanning electron microscope The deposits were isolatedfrom all organic matter by digestion with nitric and perchloricacids Two basic types of deposits were recognized, lumen andwall silicification, the latter with or without lumen infillings In the culm internodes, lumen deposits are derived from idioblasts(‘hats’), sclerenchyma and xylem vessels In thefloral bracts they are derived from idioblasts (‘hats’and astenform opals), epidermal long cells (dendriform opals),sclerenchyma and xylem vessels The shape of these deposits doesnot generally resemble the outline of the cell itself, but depositsderived from cell walls do closely resemble the infact cell.In the culm, the walls of stomatal cells, trichomes and, largelythe outer tangential walls of mature long epidermal cells, becomesilicified, together with some cork cells In the floral bracts,silica is found in most epidermal cell walls but is confinedto the trichomes, scutiform cells and costal epidermal cellsearly in their development At maturity concentrations of silicaare much higher in the floral bracts and awns than in the culmsand leaves The results are discussed in relation to the pattern of depositionand its possible functions. Hordeum sativum Jess, barley, silica deposits, opals, scanning electron microscopy     

Correlation between the distribution of lignin and pectin and distribution of sorbed metal ions (lead and zinc) on coir (Cocos nucifera L.)

Plant fibres are capacious for sorption of metal ions, and can be used in water cleaning. Knowledge about the sorption will help in selection of the fibre and optimisation of its chemical modification, if any. The aim of this paper is to investigate the connection, if any, between the distribution of lignin and pectin and the loading of Pb and Zn on coir (mesocarp fibres from Cocos nucifera L.). The coir consisted mainly of xylem and a fibre sheath. The lignin was evenly distributed in the cell walls of the fibre sheath, but in the xylem, there was no detectable content in the compound middle lamella, and a smaller content of lignin in the secondary walls than in the walls of the fibre sheath. The only detectable content of pectin in the fibre sheath walls was in the middle lamella, cell corners and extracellular matrix, while in the xylem, the pectin was almost evenly distributed in the wall, with a higher concentration in the middle lamella and cell corners. All cell walls facing the lacuna had a high content of pectin. The metal ions were mainly loaded on the xylem and cell walls facing the lacuna, maybe with an additional trend to be loaded on the large fibres. Lead was distributed on and across the whole secondary wall. Zinc was loaded on the secondary walls, but there was no information about the distribution across the wall. If there is a simple correlation between the loading of metal ions and the distribution of lignin or pectin, these investigations point at no correlation with lignin and a positive correlation with pectin. It has to be stressed that these conclusions are made on limited material and are therefore preliminary in nature.     

PATHWAY OF WATER MOVEMENT IN HYDROIDS OF POLYTRICHUM COMMUNE HEDW. (BRYOPSIDA)

The pathway of water movement in hydroids of Polytrichum was determined by the precipitation of an electron-dense crystal (Prussian blue) in the transpirational stream. Hydrolysed end walls appear highly water permeable since Prussian blue granules were localized within the loose fibrillar network. Electron-dense granules were found free in the lumen but not in the lateral wall or in the middle lamella. These results are compared with data from vascular plant tracheary elements.     

Leaf Structural Peculiarities in Sarcopoterium spinosum, a Seasonally Dimorphic Subshrub

Extensive investigations on the anatomy of the two leaf typesin a seasonally dimorphic subshrub revealed interesting variationsbetween summer and winter leaves. Summer leaves of Sarcopoteriumspinosum possess a thick epidermis composed of tannin-containingcells and large amounts of mucilage secreted through the innerpericlinal walls towards the mesophyll. A thick cuticle is alsopresent on the surface of the leaf. In winter leaves the epidermalcells produce no mucilage while phenolics are accumulated ingranular form only. Besides these, some other variations betweensummer and winter leaves are also discussed in respect of theability of the plant to withstand the unfavourable Mediterraneanconditions. Seasonal dimorphism, leaf anatomy, Sarcopoterium spinosum     

The suberin lamella,a possible barrier to water movement from the veins to the mesophyll ofThemeda triandra forsk

Summary Precipitation of ferrous ions by ferricyanide in transpiring leaves ofThemeda triandra Forsk. produced crystalline deposits, which were visible with the light and electron microscope. Prussian blue crystals were formed within the lumina of the tracheary elements and the apoplast, or cell wall continuum of the vascular tissues and bundle-sheath cells. Little if any deposition was noted within the lignified secondary thickenings of the tracheary elements. The localization pattern suggests that the ferrous ions moved from the lumina of the tracheary elements via the exposed primary walls. Prussian blue crystals were abundant in the outer tangential and radial walls of the bundle-sheath cells. By contrast, crystals were lacking in the walls of neighbouring mesophyll cells, suggesting that the suberin lamella in the bundle-sheath walls effectively inhibited the apoplastic movement of ferrous ions and possibly may impede, or restrict the movement of water across the bundle-sheath/mesophyll interface.     

Transpiration Stream of Desert Species: Resistances and Capacitances for a C3, a C4, and a CAM Plant

Transpiration rates and water potentials of three sympatricdesert perennials, a C3 subshrub (Encelia farinosa), a C₄ bunchgrass(Hilaria rigida), and a CAM succulent (Agave deserti), wereanalysed using an electrical circuit analogue that includedresistances and capacitances for the leaves, stems, and roots.The water storage capability of the organs differed considerably,capacitance ranging over 1000-fold from the thin leaves of H,rigida to the massive leaves of A. deserti, although the capacitanceper unit volume varied only 1.9-fold. The diurnal changes inwater storage could support maximum transpiration rates of H.rigida for 4 min, E. farinosa for 7 min, and A. deserti for16 h. The time constant for equilibration of water from storageto the xylem ranged from 29 s for roots of H. rigida to 52 minfor leaves of A. deserti. Resistances for such movement wererelatively low for the succulent leaves of A. deserti and wereup to about 50-fold higher for the three organs of E. farinosa.Xylem resistances calculated using the Hagen-Poiseuille lawand measured xylem dimensions were 2.1- to 2.1-fold lower thanresistances estimated from observed water potential drops, adiscrepancy which is in agreement with other published data.Contrary to data on other plants, the xylem resistances in theroots and leaves of E. farinosa and H. rigida averaged only15% of the stem xylem resistance. Key words: Capacitance, Xylem resistance, Transpiration stream, Desert     

The leaf internal morphology and ultrastructure of Zostera muelleri irmisch ex aschers. (Zosteraceae): a comparative study of the intertidal and subtidal forms

The leaf anatomy, histochemistry and ultrastructure of the intertidal and subtidal seagrass Zostera muelleri Irmish ex Aschers. from Westernport Bay, Victoria were studied. Unusual anatomical and ultrastructural features are compared with other seagrasses and their functional significance is assessed. Subcuticular cavities are present in the young blade, but not observed in the older blade nor young and old leaf sheath. Wall ingrowths occur in the blade epidermal cells particularly on the inner tangential walls and the lower portions of the radial walls. Plasmodesmata are present between adjacent epidermal cells and between the epidermal and mesophyll cells, suggesting that solutes could transfer between these tissues both symplastically and apoplastically. Each leaf has three longitudinally aligned vascular bundles, each of which comprises a single xylem element isolated from the phloem tissue. The phloem consists of nacreous-walled sieve elements accompanied by phloem parenchyma cells which also process wall ingrowths. The xylem walls are completely hydrolysed and the middle lamella borders directly on the xylem lumen. Leaves have prominent air lacunae bisected transversely by septa at regular intervals along their length. Each septum consists of a file of small parenchyma cells with wall protuberances projecting into intercellular space. There are no major structural differences between the subtidal and intertidal plants, but the former have larger leaves and more leaves per shoot than the latter. In addition, a network of unusual reticulated fungal hyphae is present in the leaf intercellular spaces of the subtidal form and this network may facilitate solute transfer in these plants.     

Herbaspirillum, an endophytic diazotroph colonizing vascular tissue 3Sorghum bicolor L. Moench

Leaves of Sorghum bicolor were examined at 5 d and 14 d afterinoculation with the N₂-fixing endophytic bacteria Herbaspirillumseropedicae and Herbaspirillum rubrisubalbicans. Plants inoculatedwith H. rubrisubalbicans expressed symptoms of ‘red stripedisease’ i.e. red stripes along the secondary veins ofthe leaf blade close to the inoculation point and spreadingup the leaves. Infected leaves showed dense colonization byH. rubrlsubalbicans in regions showing red stripe symptoms at5 d after inoculation. The infection was confined within thevascular system, in particular, the protoxylem and associatedlacunae, which were often completely filled with bacteria, withsome of the latter expressing nitrogenase. The bacteria wererecognized using H. rubrisubalbicans-speciflc antibodies andimmunogold labelling, which also showed that the antibody reactedwith material on the surface of the bacteria, and that thismucus was released into the lumen of the xylem. At 14 d afterinoculation, disease symptoms were slightly more severe, withboth meta- and protoxylem being even more heavily colonizedin parts of the leaf showing red stripes. However, a stronghost defence response was also apparent at this stage, withgums lining the walls of the vessels and enclosing the bacteria,although the latter were still actively dividing. At the edgesof visible disease symptoms, plant gums filled the xylem; bacteriahad formed distinct colonies within these gums, with some ofthe colonies associated with the xylem walls. Plants inoculatedwith H. seropedicae either did not express the disease or showedvery mild symptoms close to the inoculation point. In the lattercase, H. seropedicae were localized within protoxylem vesselsand the metaxylem was partly occluded with plant-derived gums.By contrast with H. rubrisubalbicans, H. seropedicae was alsolocalized in leaves at 14 d without disease symptoms and didnot always appear to elicit a host response, i.e. they colonizedthe walls of metaxylem, with the xylem vessels themselves remainingunoccluded and largely free of gums. The fine line separatingplant pathogens, endophytes and symbioses is discussed in lightof these results. Key words: Herbaspirillum, Sorghum bicolor, nitrogen fixation, endophyte, xylem     

Water Movement and Storage in a Desert Succulent: Anatomy and Rehydration Kinetics for Leaves of Agave deserti

Smith, J. A. C. and Nobel, P. S. 1986. Water movement and storagein a desert succulent: anatomy and rehydration kinetics forleaves of Agave deserti.—J. exp. Bot. 37: 1044–1053. Anatomic and kinetic aspects of water storage were investigatedfor the succulent leaves of the desert CAM plant, Agave deserti.An approximately linear relationship was found between the numberof vascular bundles and leaf surface area, both for leaves ofdifferent sizes and also along the length of a single leaf.The bundles, which were distributed throughout the leaf cross-section,were separated from each other by about eight water-storagecells. Even though the cell walls of the water-storage groundtissue made up only 2?5% of the cell volume, they provided about10% of the total cross-sectional area available for water transportradial to the xylem because cell-cell contact in such a directionaveraged 25% of the cell surface area. The rehydration kineticsof partially dehydrated leaf segments were resolved into threephases: (1) a relatively rapid movement into the vascular tissue(half-time of 2 min); (2) water movement into storage in theground tissue (half-time of 59 min); and (3) water movementinto the intercellular air spaces (half-time of about 10 h).Using the observed kinetics for water movement into the storagetissue and standard diffusion theory, the bulk-averaged diffusivityof water in the relatively homogeneous ground tissue (D₁) was2?0 ? 10^–10 m² s^–1 Using this (D₁) and pathway analysis,most of the water moving from the xylem into storage in themassive leaves of A. deserti apparently occurred from cell tocell across the cell membranes rather than through the cellwalls. Key words: Agave deserti, capacitance, diffusivity, leaf anatomy, succulence, water storage     

SUBEPIDERMAL AIR SPACES: BASIS FOR THE PHENOTYPIC EXPRESSION OF THE ARGENTEUM MUTANT OF PISUM

The Argenteum (Arg) mutant of pea is characterized by a gray-green, silvery cast of the leaves and stipules. Light and electron microscopy showed that the nature of the silvery cast was due to extensive intercellular air space between the epidermis and palisade parenchyma. Adaxial epidermal strips from mutant leaves were free of palisade cell wall fragments, whereas similar strips from normal leaves had remnants of the torn palisade cells attached to the epidermal cell walls. The periphery of the epidermal-palisade cell wall interfaces showed a more electron-opaque middle lamella in the normal leaves than in the Arg mutant leaves.     

The Distribution of Silicon Deposits in the Roots of Molinia caerulea (L.) Moench. and Sorghum bicolor (L.) Moench.

The occurrence of silica in relation to meristematic zones andthe thickening of the endodermis in the roots of Molinia caerulea(L.) Moench. and Sorghum bicolor (L.) Moench. has been investigatedby means of the electron-probe microanalyser and the scanningelectron microscope. In proximal regions of mature roots ofM. caerulea, the central strengthening tissue of the stele,the vessel walls, the endodermis and the sub-epidermal sclerenchymaare areas of heavy accumulation. The distal regions of suchroots are relatively free of silicon and show little thickeningof the inner tangential walls of the endodermis or of the cellsof the strengthening tissues. The thickening of these elementsis shown to be associated with their location and the age ofthe root. In the proximal regions of S. bicolor, silicon is detected andlargely confined to the inner tangential walls of the endodermiswhich display some thickening. In addition, discrete and evenly-distributeddeposits varying in size partly fill the lumen of this layer.Some cells exhibit a number of smaller protrusions. High magnificationsof these lumen deposits show a distinct granular structure incontrast to the very uniform pattern of the wall deposits. The results are compared with deposits in grass leaves and inflorescencebracts and in woody perennials. The presence of silicon in additionto suberin, lignin and polyphenols in the thickened endodermalwall is also discussed in relation to the recognized functionof the endodermis.     

Water Pathways in Higher Plants: III. THE TRANSPIRATION STREAM WITHIN LEAVES

Water in the transpiration stream is distributed throughoutthe leaves in the vascular bundles. In wheat, water appearsto be confined to the main veins by the mestome sheath and toenter the mesophyll through the walls of the smaller veins.Within the mesophyll the water in the transpiration stream movesin the free space of the cell walls to the evaporating surfacesof the leaf. The lead chelate, which is used to trace the transpirationstream, accumulates at the final points of evaporation at themargin of the leaf. Lead chelate accumulates beneath and onthe surface of the cuticle, being partly associated with theanticlinal walls of the epidermal cells, the walls of the stomatalguard cells and specialized epidermal cells. Chelate does notaccumulate at the base of substomatal cavities, indicating thatthe cuticle of the epidermis is the main evaporating surfaceof the leaf. The behaviour in broad bean, laurel, and plantainis essentially the same. The rate of peristomatal and cuticulartranspiration is closely related to the size of the stomatalaperture. Conditions which control stomatal aperture also causechanges in the dimensions of the epidermal cells.     

Alfalfa Stem Tissues: Cell-wall Development and Lignification

Alfalfa stems contain a variety of tissues with different patternsof cell-wall development. Development of alfalfa cell wallswas investigated after histochemical staining and with polarizedlight using light microscopy and scanning electron microscopy.Samples of the seventh internode, from the base of stems grownon cut stems, were harvested at five defined stages of developmentfrom early internode elongation through to late maturity. Internodeseven was elongating up to the third sample harvest and internodediameter increased throughout the entire sampling period. Chlorenchyma,cambium, secondary phloem, primary xylem parenchyma and pithparenchyma stem tissues all had thin primary cell walls. Pithparenchyma underwent a small amount of cell-wall thickeningand lignification during maturation. Collenchyma and primaryphloem tissues developed partially thickened primary walls.In contrast to a recent report, the formation of a ring shaped,lignified portion of the primary wall in a number of cells inthe exterior part of the primary phloem was found to precedethe deposition of a thick, non-lignified secondary wall whichwas degradable by rumen microbes. In numerous xylem fibres fromthe fourth harvest date onwards, an additional highly degradablesecondary wall layer was deposited against a previously depositedlignified and undegradable secondary wall. The pattern of lignificationobserved in alfalfa stem tissues suggests that polymerizationof monolignols by peroxidases at the luminal border of the primarycell wall creates an impermeable zone which restricts lignificationof the middle lamella region of tissues with thick primary walls.Copyright1998 Annals of Botany Company Alfalfa,Medicago sativaL., stem tissue, cell wall, development, lignification, degradation.     

Water pathways in wheat leaves. III. The passage of the mestome sheath and the function of the suberised lamellae

The fluorochrome sulphorhodamine G, when present in the transpiration stream in wheat leaves, passes rapidly out of the veins and produces fluorescence in the mesophyll and epidermal cell walls. The path of movement of the dye out of the tracherary elements and across the mestome sheath to the parenchyma sheath cells was followed by rapid freezing, freeze-subsitution, dry embedding in resin, sectioning and epifluorescence microscopy. The sulphorhodamine solution was visible in tracheary elements, and, where it had passed out of the tracheary elements, strongly fluorescent in some of the cell walls. The patterns of wall fluorescence are used to chart the movements of water from the xylem through some of the radial walls of mestome sheath cells near the xylem to the free space of the mesophyll. The suberised lamellae of the mestome sheath cells must form an incomplete barrier near the xylem to permit passage of the dye. A hypothesis is formulated that the function of the suberised lamellae is to keep separate the oppositely directed fluxes of water and assimilates through the sheath. It is further proposed that the function of pits in living cells is a similar insulation of the symplastic traffic from the wayward waters of the apoplast.     

杜仲次生木质部分化过程中木质素与半纤维素组分在细胞壁中分布的动态变化

利用紫外光显微镜、透射电子显微镜结合免疫胶体金标记,研究了杜仲（Eucommia ulmoides Oliv.)次生木质部分化过程中木质素与半纤维素组分（木葡聚糖和木聚糖）在细胞壁分布的动态变化。在形成层及细胞伸展区域,细胞壁具有木葡聚糖的分布,而没有木聚糖和木质素沉积,随着次生壁S1层的形成,木质素出现在细胞角隅和胞间层,木聚糖开始出现在S1层中,此时木葡聚糖则分布在初生壁和胞间层;随着次生,壁S2层及S3层的形成和加厚,木质逐逐步由细胞角隅和胞间层扩展到S1、S2和S3层,其沉积呈现出不均匀的块状或片状沉积模式,在次生壁各层形成与其木质化的同时,木聚糖逐渐分布于整个次生壁中,而木糖聚糖仍局限分布于初生壁和胞间层。结果表明,随着细胞次生壁的形成与木质化,细胞壁结构发生较大变化。细胞壁的不同区域,如细胞角隅、胞间层、初生壁和次生壁各层,具有不同的半纤维素组成,其与木质等细胞壁组分结构构成不同的细胞壁分子结构。     

Dynamic Changes in Distribution of Lignin and Hemicelluloses in Cell Walls During Differentiation of Secondary Xylem in Eucommia ulmoides (in English)

The dynamic changes in the distribution of lignin and hemicelluloses (xylans and xyloglucans) in cell walls during the differentiation of secondary xylem in Eucommia ulmoides Oliv. were studied by means of ultraviolet light microscopy and transmission electron microscopy combined with immunogold labelling. In the cambial zone and cell expansion zone, xyloglucans were localized both in the tangential and radial walls, but no xylans or lignin were found in these regions. With the formation of secondary wall S1 layer, lignin occurred in the cell corners and middle lamella, while xylans appeared in S1 layer, and xyloglucans were localized in the primary walls and middle lamella. In pace with the formation of secondary wall S2 and S3 layer, lignification extended to S1, S2 and S3 layer in sequence, showing a patchy style of lignin deposition. Concurrently, xylans distributed in the whole secondary walls and xyloglucans, on the other hand, still localized in the primary walls and middle lamella. The results indicated that along with the formation and lignification of the secondary wall, great changes had taken place in the cell walls. Different parts of cell walls, such as cell corners, middle lamella, primary walls and various layers of secondary walls, had different kinds of hemicelluloses, which formed various cell wall architecture combined with lignin and other cell wall components.