Primary xylem ofscilla hyacinthoides (liliaceae)— the wool-bearing bulb of theophrastus

The “wool” of bolbos ho eriophoros described by Theophrastus in his Historia plantarum or Enquiry into plants is the primary xylem of the bulb scales of Scilla hyacinthoides (Liliaceae). When bulb scales are pulled apart transversely the gyres of the helical secondary wall deposited on the thin primary wall of the waterconducting elements are stretched and appear to be woolly threads.     

Occurrence of plasmodesmata between differentiating vessels and other xylem cells inSorbus torminalis L. Crantz and their fate during xylem maturation

Summary The development of pit-pairs between differentiating xylem cells has been examined by transmission electron microscopy in young shoots ofSorbus torminalis. In some vessel-to-tracheid pits, as well as in previously studied intertracheid pits, a thickening of the pit membrane containing branched plasmodesmata was observed. A secondary wall-like cap was deposited over the thickening prior to cytoplasmic autolysis; some plasmodesmata, parallel to the plane of section, appeared to perforate the cap. At the end of the cell maturation stage, the central part of the primary wall thickening was hydrolysed, while the cap, including plasmodesmata remnants, appeared unaltered. In half-bordered pit-pairs between a parenchyma cell and a vessel or a tracheid, similar structures could be observed beside the conducting elements. When the vessel or tracheid matured, sealing of the pit membrane plasmodesmata resulted from the formation of a protective layer on the parenchyma-side rather than from the deposition of a cap on the conducting cell-side. These observations provide the first information on the presence of symplasmic connections in pits between differentiating vessels and neighbouring xylem cells. InS. torminalis, xylem differentiation is probably highly coordinated within a symplasmic domain; the persistence of such connections may account for the lack of specialization ofSorbus wood.     

A single spiral artefact in Arthropod cuticle

Spirals are often seen in sections transverse to the axes of bumped structures in arthropod cuticle. (Sections through arthropod cornea or exocones yield excellent examples.) As arthropod cuticle has a helicoidal architecture (Bouligand, 1965), it might be expected that the spirals are a simple consequence of that structure. According to a symmetry argument, the spirals thus predicted must be double spirals. In contrast, the observed spirals are usually single. We propose that the single spirals result from an interaction between the microtome knife and the cuticle architecture. The direction of knife travel defines an orientation within the cuticle, subverting the symmetry arguments that require double spirals. Bouligand (1972) presented a model for the interaction of the knife with the cuticle. However, we offer arguments and observations which show that Bouligand's model is incorrect. We argue from detailed observations of the single spiral that it is indeed a knifing artifact and that its explanation probably lies within a certain class of models. Two related models based on relative movements of cuticle components are examined via computer techniques.     

LIGHT AND ELECTRON MICROSCOPE STUDIES OF THE PRIMARY XYLEM OF RICINUS COMMUNIS

Scott , Flora Murray , Virginia Sjaholm, and Edwin Bowler (U. California, Los Angeles.) Light and electron microscope studies of the primary xylem of Ricinus communis. Amer. Jour. Bot. 47(3) : 162-173. Illus. 1960.–The development of annular and spiral vessels in Ricinus communis has been examined under light and electron miscroscopes. Under the light microscope it is seen that spiral elements make up the bulk of the primary xylem. Pits and plasmodesmata are ubiquitous and are demonstrable in vertical and end walls. Plasmodesmata are evident in spiral thickenings. During tissue growth, intercellular spaces are formed between surrounding cells and developing vessels. These circum-vessel spaces are first lined with and later occluded by suberinlike substances. Traces of a material similar in microchemical reaction are laid down in the middle lamella. A suberin-like lining, termed in this paper the lipid lining, stainable with dimethylaminoazobenzene, occurs in mature living vessel elements. Innumerable minute fat-like droplets, refringent, and stainable with Sudan III, Sudan Black and also with osmic acid, occur in the outer cytoplasm and appear to be attached to the vessel lining by fine protoplasmic strands. They presumably are the source of the wall deposits. After the death of the protoplast, the vessel walls appear completely suberized. When contiguous cells are removed by treatment with I₂ki-H₂SO₄, their site and the site of the intercellular spaces remain marked by linear suberized ridges on the vessel wall. Annular and spiral thickenings arise as cellulose strands and begin to lignify only when the vessel reaches maximum diameter. In transverse section, the broken end of an extracted spiral thickening appears stratified. Under the electron microscope, pits and plasmodesmata are evident in procambial and in differentiating xylem elements in all walls. Annular and spiral thickening are distinguishable first as closely woven microfibrillar cellulose bands. As lignin is deposited in the microfibrillar mesh, the thickenings become dense to the electron beam. Irradiation with the full strength of the electron beam distinguishes between spiral thickenings in younger and older vessels. Older spirals remain apparently unchanged. Younger spirals instantly swell, volatilize in part, and assume a moniliform outline. The bead-like swellings consist of a matrix partly transparent to the electron beam and an internal framework of a material comparatively dense to the electron beam. Similar intense irradiation differentiates between younger and older vessel linings. Older linings appear unchanged, while the younger react violently, volatilize in part and stabilize as an irregular coagulum set in a basic mesh. The volatilized substances appear as granules on lining surface or on substrate. The changing microfibrillar pattern of the cell wall is observed from the procambial stage to the final deposition of the lipid vessel lining.     

Strukturelle Grundlagen des Parasitismus beiOrobanche III. Die Differenzierung des Xylemanschlusses beiO. crenata

Zusammenfassung Innerhalb des Wirtsxylems wurden Haustorialzellen des WurzelparasitenOrobanche lichtund elektronenoptisch untersucht. Diese Zellen durchlaufen eine ungewöhnliche Differenzierung bis sie wasserleitendes Xylemanschlu\element sind. Von Haustorialzellen mit stark verdickten FrontwÄnden entwickeln sie sich bei Eintritt in das Wirtsxylem zu einer typischen Transferzelle mit polar zum Holzelement des Wirts angelegtem Wandlabyrinth. Erst durch einen zweiten Differenzierungsschritt wird die Transferzelle zum Wasserleitelement, indem die typischen SekundÄrwandverdickungen des Xylems in der Zelle angelegt werden. Diese entstehen teilweise innerhalb des Wandlabyrinths und sind stets gegenüber denjenigen des Wirtselements angelegt. Zuletzt wird das Labyrinth — bis auf gelegentliche Reststrukturen — abgebaut, der Protoplast degeneriert, und es entsteht ein haustoriales Wasserleitelement, das über kommunizierende Tüpfel an das Wirtselement angeschlossen ist.

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Structural features of parasitism ofOrobanche III. The differentiation of xylem connexion ofO. crenata

Summary Haustorial cells of the root parasiteOrobanche within the xylem of the host tissue were investigated by light- and electronmicroscopy. Coming into contact with the tracheary elements of the host these cells show an unusual differentiation before turning into a water conducting xylem element. From haustorial cells with thickened front walls they develop into typical transfer cells, bearing wall ingrowth in those parts of the wall orientated towards the tracheary elements of the host. During further differentiation the transfer cell changes into a water conducting element by developing the typical secondary wall thickenings of xylem elements within the cell. Partly these wall thickenings are formed inside the labyrinth structures of the transfer cell, always situated opposite those of the tracheary element of the host. Simultaneously the labyrinth disintegrates—some small remnants of wall ingrowths may persist. The protoplast degenerates, and finally a haustorial water conducting element results. Host- und parasitic tracheary elements are connected by pits.

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Wir danken FrauChristl Glockmann für ihre stets verantwortungsvolle Mitarbeit. Den GÄrtnern des Botanischen Gartens in Kiel sei Dank für die oft schwierige Anzucht des Pflanzenmaterials. Die Untersuchungen wurden durch Mittel der Deutschen Forschungsgemeinschaft gefördert.     

Some aspects of organization and histochemistry of the embryo sac ofScilla sibirica sato

Summary The present investigation deals with some of the organizational and histochemical aspects of the embryo sac ofScilla sibirica. Both the synergids and egg cell are invested by PAS-positive complete walls. The filiform apparatus comprises an elaborate system of fibrillar projections, showing extensive ramifications. The micropylar region of the embryo sac wall from where the filiform apparatus originates is composed of three distinct layers. On a histochemical basis it may be surmised that, unlike the egg cell, the synergids are metabolically very active. Two kinds of wall ingrowths (i) massive and highly branched very much akin to the filiform apparatus, and (ii) small tuberculate wall projections, are unique to the antipodal cells of S.sibirica. Small tuberculate projections have also been observed along the wall of the central cell adjacent to the nutrient-rich nucellar cells. The antipodals and the central cell show the presence of starch grains and abundant total proteins. All the cell types in the embryo sac ofS. sibirica are structurally so organized as to meet the requirements of its nutrition during pre- and postfertilization development. The presence of abundant PAS-positive granular substance in the cells of nucellar epidermis probably establishes a gradient which assists in the pollen tube growth.     

Ultrastructure of the haustorial interface and apoplastic continuum between host and the root hemiparasiteOlax phyllanthi (Labill.) R. Br. (Olacaceae)

Summary Structural features of haustorial interface parenchyma of the root hemiparasiteOlax phyllanthi are described. Walls contacting host xylem are thickened non-uniformly with polysaccharides, not lignin, and show only a thin protective wall layer when abutting pits in walls of host xylem vessels or tracheids. Lateral walls of interface parenchyma exhibit an expanded middle layer of open fibrillar appearance, sometimes with, but mostly lacking adjoining layers of dense wall material. Free ribosomes and rough endoplasmic reticulum are prominent and occasional wall ingrowths present. Experiments involving transpirational feeding of the apoplast tracers lanthanum nitrate or uranyl acetate to host roots cut below haustorial connections, indicate effective apoplastic transfer from host to parasite root via the haustorium. Deposits of the tracers suggest a major pathway for water flow through host xylem pits, across the thin protective wall layer, and thence into the haustorium via the electronopaque regions of the terminal and lateral walls of the contact parenchyma. Graniferous tracheary elements and walls of parenchyma cells of the body of the haustorium appear to participate in tracer flow as do walls of cortical cells, stele parenchyma and xylem conducting elements of the parasite root, suggesting that both vascular and non-vascular routes are involved in extracytoplasmic transfer of xylem sap from host to parasite. The Casparian strip of the endodermis and the suberin lamella of the exodermis of theOlax root act as barriers to flow within the system.     

THE FERTILIZATION CANAL IN PLODIA INTERPUNCTELLA (HÜBNER) (PYRALIDAE: LEPIDOPTERA)

The spermathecal duct of Plodia interpunctella (Hübner) was studied with light and transmission electron microscopy. The lumen in the duct is enclosed by a thin chitinous wall that has a thicker band that spirals along the length of the duct. The thick spiral band pinches off part of the lumen and creates a smaller canal, which it encloses. Although the two canals are not separated, the duct appears to have a double lumen. The thin wall of the main canal provides a flexibility in which the lumen widens or narrows concomitantly with contractions of the spermatheca and the portion of the duct adjoining the spermatheca. Sperm is transferred from the spermatheca to the vestibulum where the egg is fertilized. The distention of the canal and contractions of the spermatheca thus account for the speed at which eggs are fertilized and deposited.     

Ultrastructure of transfer cells in spontaneous nodules of alfalfa (Medicago sativa)

Summary Spontaneous nodules were formed on the primary roots of alfalfa plants in the absence ofRhizobium. Histologically, these white single-to-multilobed structures showed nodule meristems, cortex, endodermis, central zone, and vascular strands. Nodules were devoid of bacteria and infection threads. Instead, the larger cells were completely filled with many starch grains while smaller cells had very few or none. Xylem parenchyma and phloem companion cells exhibited long, filiform and branched wall ingrowths. The characteristic features of both types of transfer cells were polarity of wall ingrowths, high cytoplasmic density, numerous mitochondria, abundant ribosomes, well-developed nucleus and nucleolus, and vesicles originated from rough endoplasmic reticulum. These results were compared with normal nodules induced byRhizobium. Our results suggest that xylem parenchyma and phloem companion transfer cells are active and probably involved in the short distance transport of solutes in and out of spontaneous nodules. Since younger nodules showed short, papillate, and unbranched wall ingrowths, and older tissue showed elongated, filiform and branched wall ingrowths, the development of wall ingrowths seemed to be gradual rather then abrupt. The occurrence of both type-A and -B wall ingrowths suggests that phloem companion transfer cells may be active in loading and unloading of sieve elements. Since there were no symbiotic bacteria and thus no fixed nitrogen, it is tempting to speculate that xylem parenchyma transfer cells may be re-transporting accumulated carbon from starch grains to the rest of the plant body by loading xylem vessels. Fusion of ER-originated vesicles with wall ingrowth membrane indicated the involvement of ER in the membrane formation for elongating wall ingrowths. Since transfer cells were a characteristic feature of both spontaneous andRhizobium-induced nodules, their occurrence and development is controlled by the genetic make-up of alfalfa plant and not by a physiological source or sink emanating from symbiotic bacteria.Abbreviations ATP adenosine triphosphate - ATPase adenosine triphosphatase - EH emergent root hair - EM electron microscope - Nar nodulation in the absence of Rhizobium - RT root tip - RER rough endoplasmic reticulum - YEMG yeast extract mannitol-gluconate     

The duct connecting Malpighian tubules and gut: an ultrastructural and comparative analysis in various Ephemeroptera nymphs (Pterygota)

Malpighian tubules proper are connected to the gut by ducts called trunks, the organization of which is described at ultrastructural level in the nymphs of various mayfly species, namely Ecdyonurus venosus (Heptageniidae), Ephemerella ignita (Ephemerellidae), Choroterpes picteti (Leptophlebiidae), and Caenis luctuosa (Caenidae). Trunks are luminal tubes varying in arrangement, number, shape, and length. The main cell type of the trunk wall is represented by cells that are bordered by a thin cuticle along their luminal side (type-A cells). Whereas these cells are exclusive in the long trunks (such as those of C. picteti and C. luctuosa), in the shorter ones (such as those of E. venosus and Ephemerella ignita) cells with a microvillous luminal border (type-B cells) are also encountered. These cells are located close to the entrance of the collecting duct of the Malpighian tubules proper, and their long microvilli form a dense filamentous mesh filling up the lumen. Both cell types exhibit fine structural features that are characteristics of ion-transporting epithelia. Ultrastructural investigations show that trunks are not a simple conducting system but are involved in the regulation of the ionic composition of the primary urine for producing a fluid hypo-osmotic with respect to the hemolymph. Accepted: 30 May 2000     

Xylem parenchyma cells deliver the H<Subscript>2</Subscript>O<Subscript>2</Subscript> necessary for lignification in differentiating xylem vessels

Lignification in Zinnia elegans L. stems is characterized by a burst in the production of H₂O₂, the apparent fate of which is to be used by xylem peroxidases for the polymerization of p-hydroxycinnamyl alcohols into lignins. A search for the sites of H₂O₂ production in the differentiating xylem of Z. elegans stems by the simultaneous use of optical (bright field, polarized light and epi-polarization) and electron-microscope tools revealed that H₂O₂ is produced on the outer-face of the plasma membrane of both differentiating (living) thin-walled xylem cells and particular (non-lignifying) xylem parenchyma cells. From the production sites it diffuses to the differentiating (secondary cell wall-forming) and differentiated lignifying xylem vessels. H₂O₂ diffusion occurs mainly through the continuous cell wall space. Both the experimental data and the theoretical calculations suggest that H₂O₂ diffusion from the sites of production might not limit the rate of xylem cell wall lignification. It can be concluded that H₂O₂ is produced at the plasma membrane in differentiating (living) thin-walled xylem cells and xylem parenchyma cells associated to xylem vessels, and that it diffuses to adjacent secondary lignifying xylem vessels. The results strongly indicate that non-lignifying xylem parenchyma cells are the source of the H₂O₂ necessary for the polymerization of cinnamyl alcohols in the secondary cell wall of lignifying xylem vessels.     

Ultrastructural observations on the gills of polychaetes

The gills of several polychaete species belonging to 9 families were studied by scanning and transmission electron microscopy. The surface epithelium is covered by a thin cuticle which is invaded by microvilli penetrating the epicuticle in certain species. Some epithelial cells bear cilia, others are mucus-producing cells. The ciliary cells may be arranged in rows and maintain a constant flow of water over the gills. The distance between external water and blood stream differs considerably according to the species investigated. InMalacoceros the gills are characterized by closed afferent and efferent subepithelial vessels, which correspond to tubular invaginations of the coelomic wall. These vessels are lined by the basement lamina of the coelothelial cells, which are of the epitheliomuscular type. The vessels are open in the gills of other polychaetes and release the blood stream into a system of spaces immediately below the epidermis (e.g. in the branchial lamellae ofPectinaria andTerebellides). In several species the blood comes into very intimate contact with the cuticle (e.g. in the gill filaments ofDendronereides), but also in these animals both are separated by a very small epidermal layer.Supported by DFG Sto 75/3-6.     

Structural and Histochemical Features of the Slow-Growing Perennial <i>Coptis chinensis</i> Franch. (Ranunculaceae)

Huanglian (Coptis chinensis Franch.) is a slow-growing perennial medicinal herb with considerable economic value. This study aimed to determine the structural characteristics and the levels of berberine deposits in the organs and tissues of Huanglian using light and epifluorescence microscopy. The adventitious roots are composed of primary and secondary structures with endodermis, exodermis, and phellem. The rhizome structures are composed of primary and secondary structures with cuticle and phellem. The leaves are composed of sclerenchymatous rings, isolateral mesophyll, and thin cuticles. We detected berberine in the xylem walls of the roots and rhizomes as well as in the sclerenchymatous rings of the petioles. We postulate that as the exodermis is developed, the deposition of berberine in the xylem closest to the root tips may affect water and nutrient absorption and transfer. Leaf blades had a thin cuticle and isolateral mesophyll, suggesting shade tolerance. These structural and histochemical features suggest that Huanglian is adapted to the slow growing nature of a shady environment.     

Origin and development of stomatal microanatomy in two species ofEucalyptus

Summary Development of the stomata ofEucalyptus orbifolia (in which they are relatively superficial) andE. incrassata (in which they are deeply sunken) is described from light microscopy of thin sections of resin-embedded material. The envelope of the guard mother cell is retained intact while in the daughter cells (guard cells) the inner and outer thickenings are formed. The mother cell envelope may even remain discrete and intact during early stages of formation of the separation spaces, precursors of the future stomatal pore, between the thickenings. Remnants of the guard mother cell wall may be retained as parts of at least the inner stomatal ledges. Likewise, remnants of the wall which divides the mother cell persist on the maturing guard cells.Sudan III-positive materials, probably cutin, are removed from the cuticle over the mother cell soon after it is formed. The cuticle above the guard cell is finally perforated by enzymic attack forming, inE. incrassata, a large cavity outside the developing stoma into which the outer stomatal ledges grow as extensions of the upper guard cell walls.The termostiole is suggested for the aperture in the cuticle. The flanges of cuticle seen in section to bound it are termedostiolar ledges. The ostiolar ledges are to be distinguished from the outer stomatal ledges, which develop from the upper thickenings of the guard cell initials. The distinction is clear inE. incrassata (and other species with deeply sunken stomata) but not in mesophytic plants or species with superficial stomata such asE. orbifolia in which the outer stomatal ledges are fused with the cuticle.Growth of the outer stomatal ledges inE. incrassata involves transport of wall materials through an annular space, the equivalent of an ectocythode.The relevance of the observations to stomatal development in other genera is discussed.     

Cuticular surface structures in glyptonotus antarcticus — a marine isopod from the Ross Sea (Antarctica)

Summary Various types of surface microstructures and their distribution in the Giant Antarctic SlaterGlyptonotus antarcticus Eights, 1852, are described in detail. Although no attempt has been made to classify the different kinds of scales, leaf-like modifications, threads and feathery hairs, ideas concerning their origin and their function are presented. At least some of the microstructures described seem involved in discouraging foraminifera and larval stages of sessile organisms to settle upon the cuticle ofClyptonotus.     

ULTRASTRUCTURE OF THE CUTICLE OF OHELO (VACCINIUM RETICULATUM)

When viewed by electron microscopy of thin sections, the inner two-thirds of the petiolar cuticle of Vaccinium reticulatum appears dense and is penetrated by a channel-like reticulum which emanates from the primary cell wall. The outer one-third of the cuticle stains lightly and is homogeneous. This arrangement is compared with the ultrastructure of cuticle previously reported for other plant species.     

In vitro recognition of a 190 kda putative attachment receptor from the cuticle of Meloidogyne javanica by Pasteuria penetrans spore extract

Studies were undertaken to develop an improved understanding of the mechanism by which spores of Pasteuria penetrans bind to the cuticle of susceptible nematode hosts. A polyclonal antibody recognized an antigenic ladder at Mr ～ 41 kDa when Meloidogyne javanica cuticle extracts were electrophoresed in the presence of SDS and blotted on to a nitrocellulose membrane. Digestion of the cuticle extracts prior to electrophoresis with Proteinase K and lipase showed the antigenic ladder to be a protein. Attempts to block the antigenic ladder with N‐acetylglucosamine in the form of chitobiose did not prevent the binding of the antibody and the chitobiose could not be detected binding to the antigenic ladder using the lectin wheat germ agglutinin (WGA). Blots probed with Pasteuria spore extract and visualized with a polyclonal antibody to the spore showed that the spore extract did not bind to the antigenic ladder but did bind to a protein with Mr ～ 190 kDa and a much weaker band at ～ 45 kDa. An antibody to the lectin WGA (anti‐WGA) recognized the ～ 190 kDa polypeptide but this was not blocked by chitobiose. Concanavalin A also recognized the ～ 190 kDa protein and the presence of inhibitory sugars prohibited Con A from binding, showing the protein to be glycosylated. It is conjectured that the ～ 190 kDa glycoprotein present in the cuticle extract is a binding receptor involved in the attachment of Pasteuria spores to the nematode cuticle.     

Transfer cells in the vascular parenchyma of roots

Structural adaptations to increased transport activities were investigated in the cells of vascular parenchyma at the site of the lateral root junction, in non-stressed plant roots. Typical transfer cells were differentiated in dicotyledonousHelianthus tuberosus and in two different genotypes ofH. annuus, the cv. IBH166 and a decorative form. In the representatives of monocotyledonous, no structural adaptations occurred in the roots ofHordeum vulgare but small and rare cell wall protuberances were found in xylem and phloem ofZea mays inbred line VIR17. Some degree of cell wall labyrinth differentiation was seen in xylem and typical transfer cells were found in phloem of the roots of the maize hybrid CE380. The capability of vascular parenchyma to differentiate transfer cells did not depend on species, genotype, or on the growing conditions withHelianthus. On the other hand, the development of the structural adaptations in monocotyledonous representatives depended on both the species and the genotype. This capability may be linked with the taxonomic and evolutionary position of plant species.     

Regulation of plant elongation growth by surface and xylem proton pumps

The roles of plasmalemma electrogenic proton pumps in elongation growth of plant stems are discussed on the basis of growth-electrophysiological studies on hypocotyl segments ofVigna unguiculata. Plant stems usually have two spatially separated electrogenic proton pumps: the surface proton pump which is located on the surface membrane of the symplast and the xylem proton pump, on the cell membrane of the symplast/xylem apoplast boundary. The surface proton pump excretes protons into the surface cell wall layer and causes the loosening of the cell wall. The xylem proton pump excretes protons into the xylem apoplast and drives the uptake of solute and water into the symplastvia secondary and/or tertiary active mechanisms: the proton cotransport system and the apoplast canal system. Both the surface and the xylem proton pumps are active during elongation growth because both the yielding of cell wall loosening and the uptake of water are necessary for continued elongation growth.     

Zur Ultrastruktur und Funktion pollenverbindender Fäden beiEricaceae und anderen Angiospermenfamilien

Viscin threads and other pollen connecting threads of some angiosperm families were investigated, especially those ofEricaceae. According to the definition adopted, viscin threads are ± long exinous processes which consist of exinous material and connect pollen grains or tetrads. Such viscin threads are found within theOnagraceae, Caesalpiniaceae, Ericaceae, andMimosaceae only. While they differ in structure and composition, they always consist of sporopollenin and exhibit a very strong stickiness, even after all viscid substances have been removed by acetolysis. In contrast, the pollen connecting scleroprotein threads ofOrchidaceae and the cellular threads ofStrelitzia reginae Aiton. (Musaceae) are not connected with the exine surface, are destroyed by acetolysis, and thus do not correspond to viscin threads.