Cell wall composition of leaves of an inherently fast- and an inherently slow-growing grass species

Differences in the relative growth rules of the inherently slow-growing Deschampsia flexuosa L. and the inherently fast-growing Holcus lanatus L. were reflected in cell wall synthesis in the elongation zone of the leaves. Leaf elongation rates depended on the size of the plant and ranged from 6 to 14 mm d^?1 in Deschampsia and from 12 to 42 mm d^?1 in Holcus. Anatomical data showed that the epidermis and vascular tissue are the important tissues controlling leaf extension. The cell wall polysaccharides of fully expanded leaves of the two species were identical in sugar composition. Enzymatic hydrolysis of polymeric sugars in the cell walls of the sheath and the lamina gave glucose (85%), arabinose (3.5%), fucose (0.5%), xylose (5.0%), mannose (0.5%), galaclose (0.8%) and galacturonic acid (3–4%). This composition applied throughout the blade and the sheath and did not change with ageing. Polysaccharides in the meristems of the two species showed identical sugar compositions with 51–55% glucose, 13–15% galactoronic acid and 13–14% arabinose as the main components. The extension zone was marked by a gradual increase of driselase-digestable polymers (per mm tissue) and a concurrent shift in sugar composition. The massive increase of glucose in the cell wall polymers of the elongation zone is probably caused by cellulose synthesis. The rate of synthesis of cell wall polysaccharides in Holcus was twice as high as that in Deschampsia. The slower-growing Deschampsia has more ferulic acid esterified with cell walls, which might contribute to the slowing of leaf growth. Lignin is not significantly deposited until growth has essentially ceased and is not responsible for the difference in growth rate.     

Secondary cell wall deposition causes radial growth of fibre cells in the maturation zone of elongating tall fescue leaf blades

A gradient of development consisting of successive zones of cell division, cell elongation and cell maturation occurs along the longitudinal axis of elongating leaf blades of tall fescue (Festuca arundinacea Schreb.), a C3 grass. An increase in specific leaf weight (SLW; dry weight per unit leaf area) in the maturation region has been hypothesized to result from deposition of secondary cell walls in structural tissues. Our objective was to measure the transverse cell wall area (CWA) associated with the increase in SLW, which occurs following the cessation of leaf blade elongation at about 25 mm distal to the ligule. Digital image analysis of transverse sections at 5, 15, 45, 75 and 105 mm distal to the ligule was used to determine cell number, cell area and protoplast area of structural tissues, namely fibre bundles, mestome sheaths and xylem vessel elements, along the developmental gradient. Cell diameter, protoplast diameter and area, and cell wall thickness and area of fibre bundle cells were calculated from these data. CWA of structural tissues increased in sections up to 75 mm distal to the ligule, confirming the role of cell wall deposition in the increase in SLW (r2 = 0.924; P < or = 0.01). However, protoplast diameter of fibre cells did not decrease significantly as CWA increased, although mean thickness of fibre cell walls increased by 95 % between 15 and 105 mm distal to the ligule. Therefore, secondary cell wall deposition in fibre bundles of tall fescue leaf blades resulted in continued radial expansion of fibre cells rather than in a decrease in protoplast diameter.     

Phenotypic plasticity in response to nitrate supply of an inherently fast-growing species from a fertile habitat and an inherently slow-growing species from an infertile habitat

The aim of the present study was to investigate possible differences in plasticity between a potentially fast-growing and a potentially slow-growing grass species. To this end, Holcus lanatus (L.) and Deschampsia flexuosa (L.) Trin., associated with fertile and infertile habitats, respectively, were grown in sand at eight nitrate concentrations. When plants obtained a fresh weight of approximately 5 g, biomass allocation, specific leaf area, the rate of net photosynthesis, the organic nitrogen concentration of various plant parts and the root weight at different soil depths were determined. There were linear relationships between the morphological and physiological features studied and the In-transformed nitrate concentration supplied, except for the specific leaf area and root nitrogen concentration of H. lanatus, which did not respond to the nitrate concentration. The root biomass of H. lanatus was invariably distributed over the soil layers than that of D. flexuosa. However, D. flexuosa allocated more root biomass to lower soil depths with decreasing nitrate concentration, in contrast to H. lanatus, which did not respond. The relative response to nitrate supply, i.e. the value of a character at a certain nitrate level relative to the value of that character at the highest nitrate supply, was used as a measure for plasticity. For a number of parameters (leaf area ratio, root weight ratio, root nitrogen concentration, vertical root biomass distribution and rate of net photosynthesis per unit leaf weight) the potentially slow-growing D. flexuosa exhibited a higher phenotypic plasticity than the potentially fast-growing H. lanatus. These findings are in disagreement with current literature. Possible explanations for this discrepancy are discussed in terms of differences in experimental approach as well as fundamental differences in specific traits between fast- and slow-growing grasses.     

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.     

PROTOXYLEM MATURATION IN THE SEEDLING LEAF OF WHEAT

Protoxylem (PX) maturation was followed in vascular bundles of the first foliage leaf (L#1) of wheat seedlings, using clearings and sectioned materials to assess development changes. L#1 contained seven to 11 longitudinal bundles. The seven bundles with largest diameters contained PX vessels, but the number of bundles with PX varied with leaf length. Repeated vessel maturation maintained PX continuity as older vessels collapsed due to leaf extension. Thus, the number of PX vessels in each bundle was also a function of leaf length, and the PX content of a bundle was a function of the stage of leaf development and how soon during leaf development the bundle attained mature PX. Distance from the leaf tip to the start point for PX was greater for bundles later to mature. Thus, the pattern of distal start points in mature leaves reflected the progression of PX maturation from the midrib to bundles of lower rank. It is suggested that the involvement of more and more bundles in PX maturation as the leaf ages is a general occurrence in grass leaves, and that assessing how many bundles will have PX requires observations late in leaf development.     

DEVELOPMENTAL ANATOMY OF THE STEM OF WELFIA GEORGII,IRIARTEA GIGANTEA,AND OTHER ARBORESCENT PALMS: IMPLICATIONS FOR MECHANICAL SUPPORT

Changes in stem anatomy with radial position and height were studied for the arborescent palms Welfia georgii, Iriartea gigantea, Socratea durissima, Euterpe macrospadix, Prestoea decurrens, and Cryosophila albida. Vascular bundles are concentrated toward the stem periphery and peripheral bundles contain more fibers than central bundles. Expansion and cell wall thickening of fibers within vascular bundles continues throughout the life of a palm, even in the oldest tissue. Within individual vascular bundles, the fibers nearest the phloem expand first and fiber cell walls become heavily thickened. A front of expanding fibers moves outward from the phloem until all fibers within a vascular bundle are fully expanded and have thick cell walls. Peripheral vascular bundles differentiate first and inner bundles later. In the stem beneath the crown, vascular bundles and ground tissue cells show little or no size increase, but marked cell wall thickening during development for Welfia georgii. Beneath the crown, diameters of peripheral vascular bundles increase more than twofold for Iriartea gigantea, while diameters of central bundles do not increase. In Iriartea stems, ground tissue cells at the periphery elongate to accommodate expanding vascular bundles and cell walls become thickened to a lesser degree than in fibers; central ground tissue cells elongate markedly, but cell walls do not become thickened; and large lacunae form between central parenchyma cells. For Iriartea, Socratea, and Euterpe, sustained cell expansion results in limited, but significant increases in stem diameter. For all species, sustained cell wall thickening results in dramatic increases in stem stiffness and strength.     

LITTER NUTRIENT CONTENT AND PRODUCTION IN THE GREAT DISMAL SWAMP

Litter production was studied in the Great Dismal Swamp, Virginia in four plant communities which differ primarily in species composition and flooding regime. Greatest leaf deposition occured in the more flooded communities, maple-gum (Acer-Nyssa) with 536 gm^-2 yr^-1 and cypress (Taxodium distichum (L.) Richard) with 528 gm^-2 yr^-1, followed by the cedar (Chamaecyparis thyoides (L.) BSP) and mixed hardwood (Quercus-Acer-Nyssa-Liquidambar) communities, with 506 gm^-2 yr^-1 and 455 gm^-2 yr^-1, respectively. Apparently periodic flooding promotes production. Peaks occurring in October and November corresponded to autumn leaf fall, while peaks in January and May were due to some leaf litter combined with a large amount of woody litter. Litter nutrient concentrations were higher, except for Ca, in the most abundant species (cypress and water gum) in the frequently flooded cypress community. Higher leaf fall rates and litter nutrient concentrations resulted in greater nutrient deposition in the cypress and maple-gum communities.     

Comparative investigation of primary and tertiary endodermal cell walls isolated from the roots of five monocotyledoneous species: chemical composition in relation to fine structure

The chemical composition of isolated endodermal cell walls from the roots of the five monocotyledoneous species Monstera deliciosa Liebm., Iris germanica L., Allium cepa L., Aspidistra elatior Bl. and Agapanthus africanus (L.) Hoffmgg. was determined. Endodermal cell walls isolated from aerial roots of M. deliciosa were in their primary developmental state (Casparian bands). They contained large amounts of lignin (6.5% w/w) and only traces of suberin (0.5% w/w). Endodermal cell walls isolated from the other four species were in their tertiary developmental state. Lignin was still the more abundant cell wall polymer with amounts ranging from 3.8% (w/w, A. cepa) to 4.5% (w/w, I. germanica). However, compared to endodermal cell walls in their primary state of development (Casparian bands), tertiary endodermal cell walls contained significantly higher amounts of suberin, ranging from 1.8% (w/w, I. germanica) to 3.0% (w/w, A. africanus). Thus, chemical characterization of endodermal cell walls from five different species revealed that lignin was the dominant cell wall polymer in the Casparian band of M. deliciosa, whereas tertiary endodermal cell walls contained, in addition to lignin, increasing amounts of suberin (I. germanica, A. cepa, A. elatior and A. africanus). Besides the two biopolymers lignin and suberin, cell wall carbohydrates in the range of between 40 and 60% were also quantified. The sum of all cell wall compounds investigated by gas chromatography resulted in a recovery of 50–80% of the dry weight of the isolated cell wall material. Quantitative chromatographic results in combination with microscopic studies are consistent with the existence of a distinct suberin lamella and lignified tertiary wall deposits. From these data it can be concluded that the barrier properties of the endodermis towards the apoplastic transport of ions and water will increase from primary to tertiary endodermal cell walls due to their increasing amounts of suberin. Received: 23 August 1997 / Accepted: 28 January 1998     

Reduced nitrogen allocation to expanding leaf blades suppresses ribulose-1,5-bisphosphate carboxylase/oxygenase synthesis and leads to photosynthetic acclimation to elevated CO<Subscript>2</Subscript> in rice

Net photosynthetic rate (P _N) measured at elevated CO₂ concentration (C _e), ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco), and nitrogen (N) content in rice leaves decreased significantly after exposure to long term C _e. The reduction in P _N, Rubisco, and leaf N at C _e was similar for the last fully expanded leaf blade (LFELB) and expanding leaf blade (ELB). Spatial leaf N content in the ELB was highest in the zone of cell division, sharply declined as cell expansion progressed and gradually increased with cell maturation. Maximum reduction in spatial leaf N and Rubisco content was found at C _e only within cell expansion and maturation zones. The spatial leaf N content correlated well with the amount of Rubisco synthesized during leaf expansion, suggesting that N deposition into the expanding leaf blade may be the key for Rubisco synthesis and possibly photosynthetic acclimation to C _e.     

Arabinoxylan, β‐glucan and pectin in barley and malt endosperm cell walls: a microstructure study using CLSM and cryo‐SEM

The architecture of endosperm cell walls in Hordeum vulgare (barley) differs remarkably from that of other grass species and is affected by germination or malting. Here, the cell wall microstructure is investigated using (bio)chemical analyses, cryogenic scanning electron microscopy (cryo‐SEM) and confocal laser scanning microscopy (CLSM) as the main techniques. The relative proportions of β‐glucan, arabinoxylan and pectin in cell walls were 61, 34 and 5%, respectively. The average thickness of a single endosperm cell wall was 0.30 µm, as estimated by the cryo‐SEM analysis of barley seeds, which was reduced to 0.16 µm after malting. After fluorescent staining, 3D confocal multiphoton microscopy (multiphoton CLSM) imaging revealed the complex cell wall architecture. The endosperm cell wall is composed of a structure in which arabinoxylan and pectin are colocalized on the outside, with β‐glucan depositions on the inside. During germination, arabinoxylan and β‐glucan are hydrolysed, but unlike β‐glucan, arabinoxylan remains present in defined cell walls in malt. Integrating the results, an enhanced model for the endosperm cell walls in barley is proposed.     

Influence of arbuscular mycorrhizal fungi and simulated acid rain on the growth and coexistence of the grasses Calamagrostis villosa and Deschampsia flexuosa

Two grass species — Calamagrostis villosa (Chaix) J.F. Gmelin and Deschampsia flexuosa (L.) Trin. — are expanding in mountain Norway spruce (Picea abies L. Karst.) forests of Central Europe damaged by anthropogenic pollution constituted particularly of acid rain. This invasion of grasses may be caused by the higher irradiance reaching the forest floor after the pollution-induced tree defoliation. The relative abundance of the two grass species is changing during the process of forest decline. Our study investigated the effects of arbuscular mycorrhizal fungi (AMF) on the growth and coexistence of both species under simulated acid rain (SAR) and two levels of irradiance. Three microcosm experiments were conducted to investigate how both grasses are influenced by the AMF when grown separately or together interacting via extraradical mycelium (ERM). A positive growth response to inoculation with Glomus mosseae BEG 25 was found for both grass species when cultivated separately and the mycorrhizal dependence and the growth benefit for D. flexuosa was greater than for C. villosa. However, when both grass species were grown together in the rhizoboxes with separated root and hyphal compartments, the growth effect of the AMF was the opposite, i.e. C. villosa benefited more. The plants did not benefit from the AMF inoculation under the SAR treatment compared with dH2O treatment. The SAR also negatively influenced root length colonised by AMF, length of the ERM, alkaline phosphatase and NADH diaphorase activities of the ERM. The role of the ERM in transporting phosphorus between these grasses was verified by applying the radioisotope ³²P. There was a greater transport of isotopic ³²P between inoculated plants C. villosa and D. flexuosa grown in separated root compartments, as compared to non-inoculated plants. The amount of transported ³²P was low: a maximum of 3% of applied ³²P was detected in the shoots of receiver plants. Mechanical disturbance of the ERM significantly decreased the ³² P transport between plants. The ³²P transport between mycorrhizal plants was higher in the D. flexuosa to C. villosa direction than in the opposite one. Neither the SAR nor the low level of irradiance influenced the amount of transported ³²P. We discuss the role of ERM links between root systems in the coexistence of both grass species. This revised version was published online in June 2006 with corrections to the Cover Date.     

Development of mestome sheath cells in leaves ofAegilops comosa var.thessalica

Summary The development of mestome sheath cells ofAegilops comosa var.thessalica was studied by electron microscopy. Anatomical and cytological observations show that this grass belongs to the C₃ or non-Kranz plants. In the asymmetrically thickened walls of mestome sheath cells a suberized lamella is present. This lamella is deposited asynchronously. In the midrib and the large lateral bundles it appears first in the outer and inner walls and usually later in the radial walls. In the small lateral bundles its appearance is delayed in the inner walls of those cells situated on the xylem side. At maturity the suberized lamella is observed in all cell walls; however, in the small lateral bundles it is partly or totally absent from the walls of some cells situated on the xylem side. Tertiary wall formation is asynchronous as well, for it generally follows the deposition pattern of the suberized lamella.During the development of the mestome sheath cells microtubules show marked changes in their number and orientation, being fewer and longitudinal during suberin deposition. Dictyosomes are very active and may be involved in primary and tertiary wall formation. Endoplasmic reticulum cisternae are abundant and partly smooth, while plasmalemmasomes may function to reduce the plasmalemma extension. However, cytoplasmic structures that are clearly involved in suberin synthesis could not be identified.Suberized lamellae react strongly with silver hexamine. This is probably due to post-fixation with osmium tetroxide.On the basis of structural characteristics the mestome sheath may be regarded as an endodermis (cf., alsoFahn 1974). The significance of this view for water and assimilate exchange between the mesophyll and the bundle is discussed.This report represents a portion of a doctoral dissertation.     

Photosynthate partitioning in Basal zones of tall fescue leaf blades

Elongating grass leaves have successive zones of cell division, cell elongation, and cell maturation in the basal portion of the blade and are a strong sink for photosynthate. Our objective was to determine dry matter (DM) deposition and partitioning in basal zones of elongating tall fescue (Festuca arundinacea Schreb.) leaf blades. Vegetative tall fescue plants were grown in continuous light (350 micromoles per square meter per second photosynthetic photon flux density) to obtain a constant spatial distribution of elongation growth with time. Content and net deposition rates of water-soluble carbohydrates (WSC) and DM along elongating leaf blades were determined. These data were compared with accumulation of ¹⁴C in the basal zones following leaf-labeling with ¹⁴CO₂. Net deposition of DM was highest in the active cell elongation zone, due mainly to deposition of WSC. The maturation zone, just distal to the elongation zone, accounted for 22% of total net deposition of DM in elongating leaves. However, the spatial profile of ¹⁴C accumulation suggested that the elongation zone and the maturation zone were sinks of equal strength. WSC-free DM accounted for 55% of the total net DM deposition in elongating leaf blades, but only 10% of incoming ¹⁴C-photosynthate accumulated in the water-insoluble fraction (WIF ≈ WSC-free DM) after 2 hours. In the maturation zone, more WSC was used for synthesis of WSC-free DM than was imported as recent photosynthate.     

Loss of capacity for acid-induced wall loosening as the principal cause of the cessation of cell enlargement in light-grown bean leaves

Cell enlargement in primary leaves of bean (Phaseolus vulgaris L.) can be induced, free of cell divisions, by exposure of 10-d-old, red-light-grown seedlings to white light. The absolute rate of leaf expansion increases until day 12, then decreases until the leaves reached mature size on day 18. The cause of the reduction in growth rate following day 12 has been investigated. Turgor calculated from measurements of leaf water and osmotic potential fell from 6.5 to 3.5 bar before day 12, but remained constant thereafter. The decline of growth after day 12 is not caused by a decrease in turgor. On the other hand, Instron-measured cell-wall extensibility decreased in parallel with growth rate after day 12. Two parameters influencing extensibility were examined. Light-induced acidification of cell walls, which has been shown to initiate wall extension, remained constant over the growth period (days 10–18). Furthermore, cells of any age could be stimulated to excrete H⁺ by fusicoccin. However, older tissue was not able to grow in response to fusicoccin or light. Measurements of acid-induced extension on preparations of isolated cell walls showed that as cells matured, the cell walls became less able to extend when acidified. These data indicate that it is a decline in the capacity for acid-induced wall loosening that reduces wall extensibility and thus cell enlargement in maturing leaves.Abbreviations and symbols FC fusicoccin - P turgor pressure - RL red light - WEx wall extensibility - WL white light - P _w leaf water potential - P _s osmotic potential     

Microtubules and morphogenesis in ordinary epidermal cells ofVigna sinensis leaves

Summary Undifferentiated ordinary epidermal cells (ECs) ofVigna sinensis leaves possess straight anticlinal walls and cortical microtubules (Mts) scattered along them. At an early stage of EC differentiation cortical Mts adjacent to the above walls form bundles normal to the leaf plane, loosely interconnected through the cortical cytoplasm of the internal periclinal wall. At the upper ends of the Mt bundles, Mts fan out towards the external periclinal wall and form radial arrays. Mt bundles and radial arrays exhibit strict alternate disposition between neighbouring ECs. An identical reticulum of cellulose microfibril (CM) bundles is deposited outside the Mt bundles. Local wall pads rise at the junctions of anticlinal walls with the external periclinal one, where the CM bundles terminate. They display radial CMs fanning towards the external periclinal wall. The CM bundles and radial CM systems prevent local cell bulging, but allow it in the intervening wall areas. In particular, the radial CM systems dictate the pattern of EC waviness by favouring local tangential expansion of external periclinal wall. As a result, ECs obtain an undulate appearance. Constrictions in one EC correspond with protrusions of adjacent ECs. ECs affected by colchicine entirely lose their Mts and do not develop wavy walls, an observation substantiating the role of cortical Mts in EC morphogenesis.Abbreviations CM cellulose microfibril - DTT dithiothreitol - EC epidermal cell - MSB microtubule stabilizing buffer - Mt microtubule - PBS phosphate buffered saline - PMSF phenylmethylsulfonyl fluoride     

Silicon Deposition in the Roots, Culm and Leaf of Phalaris canariensis L

Silicon deposition in the roots, culm and leaf of canary grass(Phalaris canariensis L.) was investigated using light microscopy,scanning electron microscopy and electron probe microanalysis. In adventitious roots grown in solution silicon was concentratedin four endodermal walls. Silicon was not detected in the endodermisof aerial adventitious roots, but was present in the epidermisand outer cortical cell layers. Silicon deposition in the culm mainly took place in the epidermis,and particularly in epidermal papillae. The silica deposition pattern in the leaf was typical of thesub-group Festucoideae. The leaf blade showed deposits in costalprickle hairs and wavy rods, but few intercostal deposits. Inthe ligule deposition was confined to isolated groups of pricklehairs on the abaxial surface. The major sites of silica depositionin the leaf sheath were the stomatal subsidiary cells, papillaeand intercostal idioblasts. Prickle hairs were much less commonin the sheath than the blade, and costal wavy rods appearedto be absent in the sheath. Phalaris canariensis L., canary grass, silicification, root, culm, leaf, electron probe microanalysis     

Rapid and reversible modifications of extension capacity of cell walls in elongating maize leaf tissues responding to root addition and removal of NaCl

A creep extensiometer technique was used to provide direct evidence that short (20 min) and long-term (3d) exposures of roots to growth inhibitory levels of salinity (100mol m^-3 NaCl) induce reductions in the irreversible extension capacity of cell walls in the leaf elongation zone of intact maize seedlings (Zea mays L.). The long-term inhibition of cell wall extension capacity was reversed within 20 min of salt withdrawal from the root medium. Inhibited elongation of leaf epidermal tissues was also reversed after salt removal. The salt-induced changes in wall extension capacity were detected using in vivo and in vitro assays (shortly after localized freeze/thaw treatment of the basal elongation zone). The rapid reversal of the inhibition of wall extensibility and leaf growth after salt removal from root medium of long-term salinized plants, suggested that neither deficiencies in growth essential mineral nutrients nor toxic effects of NaCl on plasmamembrane viability were directly involved in the inhibition of leaf growth. There was consistent agreement between the scale, direction and timing of salinity-induced changes in leaf elongation growth and wall extension capacity. Rapid metabolically regulated changes in the physical properties of growing cell walls, caused by osmotic (or other) effects, appear to be a factor regulating maize leaf growth responses to root salinization.     

Structure and distribution of lignin in primary and secondary cell walls of maize coleoptiles analyzed by chemical and immunological probes

Lignin is an integral constituent of the primary cell walls of the dark-grown maize (Zea mays L.) coleoptile, a juvenile organ that is still in the developmental state of rapid cell extension. Coleoptile lignin was characterized by (i) conversion to lignothiolglycolate derivative, (ii) isolation of polymeric fragments after alkaline hydrolysis, (iii) reactivity to antibodies against dehydrogenative polymers prepared from monolignols, and (iv) identification of thioacidolysis products typical of lignins. Substantial amounts of lignin could be solubilized from the coleoptile cell walls by mild alkali treatments. Thioacidolysis analyses of cell walls from coleoptiles and various mesocotyl tissues demonstrated the presence of guaiacyl-, syringyl- and (traces of)p-hydroxyphenyl units besidesp-coumaric and ferulic acids. There are tissue-specific differences in amount and composition of lignins from different parts of the maize seedling. Electron-microscopic immunogold labeling of epitopes recognized by a specific anti-guaiacyl/syringyl antibody demonstrated the presence of lignin in all cell walls of the 4-d-old coleoptile. The primary walls of parenchyma and epidermis were more weakly labeled than the secondary wall thickenings of tracheary elements. No label was found in middle lamellae and cell corners. Lignin epitopes appeared first in the tracheary elements on day 2 and in the parenchyma on day 3 after sowing. Incubation of coleoptile segments in H₂O₂ increased the amount of extractable lignin and the abundance of lignin epitopes in the parenchyma cell walls. Lignin deposition was temporally and spatially correlated with the appearance of epitopes for prolinerich proteins, but not for hydroxyproline-rich proteins, in the cell walls. The lignin content of coleoptiles was increased by irradiating the seedlings with white or farred light, correlated with the inhibition of elongation growth, while growth promotion by auxin had no effect. It is concluded that wall stiffness, and thus extension growth, of the coleoptile can be controlled by lignification of the primary cell walls. Primary-wall lignin may represent part of an extended polysaccharide-polyphenol network that limits the extensibility of the cell walls.Abbreviations G, S, H guaiacyl, syringyl andp-hydroxyphenyl constituents of lignin - HRGP hydroxyproline-rich glycoprotein - LTGA lignothioglycolic acid - PRP proline-rich protein Dedicated to Professor Benno Parthier on occasion of his 65th birthdayDeceased 7 November 1996     

Combined effects of chronic ozone and elevated CO2 on Rubisco activity and leaf components in soybean Glycine max

Content and activity of Rubisco and concentrations of leaf nitrogen, chlorophyll and total non-structural carbohydrates (TNC) were determined at regular intervals during the 1993 and 1994 growing seasons to understand the effects and interactions of [O3] and elevated [CO2] on biochemical limitations to photosynthesis during ontogeny. Soybean (Glycine max var. Essex) was grown in open-top field chambers in either charcoal-filtered air (CF, 20 nmol mol^-1) or non-filtered air supplemented with 1.5 x ambient [O3] (c. 80 nmol mol^-1) at ambient (AA, 360 mol mol^-1) or elevated [CO2] (700 mol mol^-1). Sampling period significantly affected all the variables examined. Changes included a decrease in the activity and content of Rubisco during seed maturation, and increased nitrogen (N), leaf mass per unit area (LMA) and total non-structural carbohydrates (TNC, including starch and sucrose) through the reproductive phases. Ontogenetic changes were most rapid in O2-treated plants. At ambient [CO2], O3 decreased initial activity (14-64% per unit leaf area and 14-29% per unit Rubisco) and content of Rubisco (9-53%), and N content per unit leaf area. Ozone decreased LMA by 17-28% of plants in CF-AA at the end of the growing season because of a 24-41% decrease in starch and a 59-80% decrease in sucrose. In general, elevated CO2], in CF or O3-fumigated air, reduced the initial activity of Rubisco and activation state while having little effect on Rubisco content, N and the chlorophyll content, per unit leaf area. Elevated CO2 decreased Rubisco activity by 14-34% per unit leaf area and 15-25% per unit Rubisco content of plants in grown CF-AA, nd increases LMA by 27-74% of the leaf mass per unit area in CF-AA because of a 23-148% increase in starch. However, the data suggest that, at elevated [CO2], increases in starch and sucrose are not directly responsible for the deactivation of Rubisco. Also, there was little evidence of an adjustment of Rubisco activity in response to starch and sucrose metabolism. Significant interactions between elevated [CO2] and [O3] on all variables examined generally resulted in alleviation or amelioration of the O3 effects at elevated CO2. These data provide further support to the idea that elevated atmospheric CO2 will reduce or prevent damage from pollutant O3.     

Ethylene-induced microtubule reorientations: mediation by helical arrays

Pruned source-sink transport systems from predarkened plants of Amaranthus caudatus L. and Gomphrena globosa L. were used to study the localization of ¹⁴C-labeled photosynthate imported into experimentally induced sink leaves by microautoradiography. During a 6-h (Amaranthus) or a 4-h (Gomphrena) transport period, ¹⁴C-assimilates were translocated acropetally from a mature source leaf provided with ¹⁴CO₂, into a younger induced sink leaf (dark/-CO₂). In addition, a young still-expanding source leaf exposed to ¹⁴CO₂ exported ¹⁴C-assimilates basipetally into a mature induced sink leaf (dark/-CO₂). Microautoradiographs showed that imported ¹⁴C-photosynthate was strongly accumulated in the sieve element/companion cell complexes of midveins, secondary veins, and minor veins of both the mature and the expanding sink leaf. Some label was also present in the vascular parenchyma and bundlesheath cells. In petioles, ¹⁴C-label was concentrated in the sieve element/companion cell complexes of all bundles indicating that assimilates were imported and distributed via the phloem. Moreover, a considerable amount of radioactivity unloaded from the sieve element/companion cell complexes of petiolar bundles, was densely located at sites of secondary wall thickenings of differen-tiating metaxylem vessels, and at sites of chloroplasts of the vascular parenchyma and bundle-sheath cells. These observations were more striking in petioles of Gomphrena than Amaranthus.Abbreviation se/cc sieve element/companion cell