The Floral Nectaries of Hibiscus rosa-sinensis: 1. Development of the Secretory Hairs

Floral nectaries of Hibiscus rosa-sinensis occur on the lowerinner side of the fused sepals and each one consists of numerous(50000–55000) secretory hairs, occupying a cylinder-likezone completely lining the inner side of the sepals. Each hairoriginates from a single protodermal mother cell and, at maturity,it is built up of a basal cell, a stalk, 35–40 intermediatecells and a tip secretory cell. Development of protodermal cellsinto secretory hairs is asynchronous, the first cells to initiatedevelopment being those situated in the lowermost part of thecylindrical zone, and development progressing upwards. Volume increase of protodermal mother cells initiating developmentis accompanied by cell polarization manifested by organelledisplacement towards the apical region. Secretory hairs areformed through a sequence of transverse and, later on, anticlinaldivisions. Divisions of apical cells are preceded by well definedpre-prophase microtubule bands, which foreshadow the plane ofthe forthcoming division and predict with accuracy the sitesof parental walls where the new cell plate fuses at cytokinesis. Stalks consist of either one or two cells. Two-celled stalksoccur in 40 per cent of secretory hairs and derive from a transversedivision of one stalk cell; the wall formed is always depositedparallel to the proximal and distal walls, but never to thelateral ones. The significance of this mode of division is discussedin relation to the fact that lateral walls are entirely impregnatedwith a cutin-like material that blocks apoplastic movement ofsolutes. Hibiscus rosa-sinensis, nectaries, development, preprophase microtuble bands, stalk cells     

The Extrafloral Nectaries of Cotton: II. CYTOCHEMICAL LOCALIZATION OF ATPASE ACTIVITY AND CA2+ -BINDING SITES, AND SELECTIVE OSMIUM IMPREGNATION

Localization of ATPase activity in the extrafloral nectariesof cotton (Gossypium hirsutum) shows most pronounced granularstaining at the plasmalemma of the sieve tube companion cellsbelow the nectaries and at the plasmalemma of cells in the secretorypapillae, particularly in the apical cell. Staining was muchmore intense in mature, secreting nectaries than in young, non-secretingones. When CaCl₂ is included in the fixation and washing solutionswith the aim of localizing calcium binding sites, prominentamorphous electron dense globules are seen at the plasmalemmaof the cells in the papillae, but also associated with othermembranes. Both granular and amorphous deposits are seen whenstaining for Ca²⁺-ATPase activity. Selective osmium impregnationshows pronounced staining of the ER and nuclear envelope insecreting nectaries but not in young non-secreting ones. Key words: Adenosine triphosphatase, Gossypium hirsutum, Nectary, Secretion     

The Anatomy, Histochemistry and Ultrastructure of Stigmas and Styles in Commelinaceae

The anatomy and ultrastructure of stigmas in 37 species of 13genera of Commelinaceae are described. The stigmas are papillate,papillae forming a dense fringe of cells around the mouth ofthe stylar canal in most species. The papillar cell wall iscovered by an unstructured cuticle of variable thickness andis of variable thickness because of small wall ingrowths. Thecuticle and the external surface of the papillar cell wall arevariably disrupted, particularly in the mid and basal regionsof the cell. This was not found in species of the genus Aploleiaor Callisia. The cell cytoplasm possesses all major organellesexcept chloroplasts and each cell is vacuolate. In all species except Aploleia mulitiflora the style comprisesan epidermis, a cortex and a hollow, tripartite canal whichis continuous into the ovary cavity. The three vascular strandsare positioned at the apex of each canal lobe. The canal cellsare elongate and tabular and the wall abutting the canal hasingrowths. The style in Aploleia is solid and the transmittingtissue comprises cells whose walls are electron opaque. Thecytoplasms of both types of cell are similar in content althoughthere is a single, large vacuole in canal cells and many smallvacuoles in transmitting tissue. The morphology, position and histochemistry of stigmatic andstylar exudate was similar in all ‘wet’ stigmas.Most of the exudate originates from the stylar canal althoughsignificant contributions are made by the papillae in stigmasof Coleotrype, Dichorisandra and Thyrsanthemum. There is no apparent relationship between stigma structure andthe presence of self-incompatibility. Stigma papillae, stylar canal, transmitting tissue, Commelinaceae     

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     

Glandular Trichomes in Satureja thymbra Leaves

The leaves of the aromatic plant Satureja thymbra have numerousglandular trichomes of two morphologically distinct types glandularhairs and glandular scales Investigations of the anatomy ofthese glandular trichomes with serial thick sections revealedthat the glandular hairs consist of three cells a foot, stalkand head cell Glandular scales also have a unicellular footand stalk Their heads, however, are composed of 12 cells Fourof these cells are small, occupying the central region of thehead, whereas the remainder are large and peripherally arrangedMorphometric analysis showed that, in leaf surface view, glandularscales are about 17-fold larger than glandular hairs In addition,glandular scales were found to occupy 5 7 % of the entire leafsurface area In each glandular scale the total amount of essentialoil, contained within both the subcuticular space and the interiorof the secretory cells, was calculated to be 2 51 x 10^–4mm³ The volume of the essential oil produced by all glandularscales on a single mature leaf was correspondingly determinedto be 0.059 mm³ Finally, the theoretical essential oil yieldof 100 g dry leaves of S thymbra was estimated to be 3 54 %(secretory activity of glandular scales only) Satureja thymbra, glandular trichomes, morphology, morphometry     

The Ultrastructure of Glandular Trichomes ofPhillyrea latifoliaL. (Oleaceae) Leaves

The anatomy and ultrastructure of glandular trichomes at differentdevelopmental stages were investigated inPhillyrea latifoliaL.leaves by transmission electron microscopy and histochemicaltechniques. The trichome consisted of a multicellular secretoryhead, a unicellular stalk and a collecting cell surrounded byepidermal cells and spongy mesophyll cells. There were numerousplasmodesmata across the cell walls of trichome cells, and especiallybetween the stalk cell and the collecting cell. The collectingcell and stalk cell contained few chloroplasts. Mitochondria,elements of the endoplasmic reticulum and small vacuoles wereabundant in the secretory cells. Crystals were present in thesecretory cells and the collecting cell, especially at the matureand senescent stages of trichome development. As the cuticle,which covered the secretory cells, did not show pores or perforations,it is proposed that secretion occurred by accumulation of productsin subcuticular spaces followed by diffusion through the cuticle.Callose accumulation was observed between the stalk cell andthe collecting cell of senescent trichomes, especially in salt-treatedplants. Trichome ontogeny was accelerated in salt-treated plants.Copyright1998 Annals of Botany Company Cuticle;Phillyrea latifolia; secretion; transmission electron microscopy; trichome development.     

Comparative studies of the neutral sugar composition of cell wall polysaccharides between cultured cells and mother plant tissues of soybean and carrot

The cell walls obtained from cultured cells grown under variousconditions and their mother plant tissues or organs were comparedwith regard to the neutral sugar composition of polysaccharides.In the pectic fraction of cell walls from soybean hypocotyl,greater amounts of galactose than other neutral sugars weredetected, and the relative sugar ratio did not change in theelongating and non-elongating portions of the tissue. On theother hand, more arabinose than other sugars was detected inthe pectic fraction of cell walls from cultured cells from soybeanhypocotyl tissue, and no significant change in the sugar ratioof polysaccharides was found in this fraction during the cultureperiod. A higher arabinose content in cell walls from culturedcells from root tissues as compared to the mother tissues ororgans was also detected in carrot. The neutral sugar ratioof cell walls from cultured cells was similar in cells grownon agar or liquid medium, with indoleacetic acid, or with orwithout 2,4-dichlorophenoxyacetic acid (2,4-D). These factssuggest that the high arabinose content of cell walls is notcommon to the cell walls of young, growing, undifferentiatedcells, and that 2,4-D is not required for the maintenance ofthe higher content of arabinose in cell walls of cultured cells. ¹A preliminary report of this work was presented for the annualmeeting of the American Society of Plant Physiologist at OhioState University, August, 1979. [Plant Physiol., 63(5) 118 (1979)]. ⁴Department of Agricultural Chemistry, Washington State University,Pullman, Washington 99164, U.S.A. (Received October 6, 1979; )     

The Development of the Fruit Walls in Carya

Both the pistillate flowers and the developing fruits of CaryaovataandC. cordiformis are covered with secretory and protectivehairs. There are two kinds of the secretory hairs. In the morefrequent one the volatile oils are accumulated under the cuticlecovering the cells of the head. In the other the secretory substancesare accumulated inside the cells. The flowers and the developingfruits of the two investigated species have quite large emergenceson which the stomata most often occur. During the developmentof the fruit lenticels are formed in the green hull. Tanninsare accumulated not only in the green hull, but also in thecarpellary layer and in the packing tissue. There are some differences between C. ovata and C. cordiformisin the course of sclerification of the green hull. In C. cordiformisthe hull is less sclerified than in C. ovata, and the sclerificationof the carpellary layer occurs later. At a certain period ratherlarge gaps are present in the lignifying shell (in the regionsof the sutures) where the cells have thin cellulose walls. Thesegaps are partly filled with sclereids. The gaps become reducedto narrow chinks, in which the cell walls remain unlignified.The hard shell is not formed in all its width at the same time.During the process of formation of the hard fruit shell theremay arise single sclereids surrounded by thin-walled cells.Within a short time these undergo a similar modification andthe tissue becomes uniform as sclerenchyma. The sclereids ofthe hard shell have, in general, strongly folded cell walls.Owing to this they overlap each other.     

Effect of Abscisic Acid on Cell-Wall Metabolism in Guard Cells of Vicia faba L.

Cell-wall synthesis in guard cells of Vicia faba L. was examinedusing sonicated epidermal strips incubated with [¹⁴C]glucose.The cell walls of the guard cells incorporated [¹⁴C]glucoseat a lower level in the dark than in the light. Stomatal aperturein the epidermal strips was reduced by application of 1 µmabscisic acid (ABA) in the light but not in the dark. The ABAtreatment reduced the incorporation of [¹⁴C]glucose into thecell walls especially in the light. Fractionation of the labeledcell-wall components revealed that ABA inhibited the synthesisof pectic substances and cellulose, but did not affect hemicellulosesynthesis. Microautoradiographs of the cell-wall fraction ofthe epidermal strips showed that a large amount of radioactivitywas distributed at both ends of the guard cells in the absenceof ABA and that removal of pectic substances from the cell-wallfraction resulted in uniform distribution of the radioactivityin the cell walls of the guard cells. These results indicatedthat the synthesis of pectic substances was active at both endsof the guard cells and was inhibited by ABA. Measurement ofspecific activities of neutral sugars in the guard-cell wallsshowed that polymers composed of galactose underwent activeturnover and that synthesis of glucans was inhibited by ABA.These results revealed a strong correlation between the stomatalmovement and the synthesis of pectic substances and cellulosein the guard cells, suggesting that the cell-wall metabolismin the guard cells may play a role in the regulation of stomatalmovement. (Received October 9, 1987; Accepted March 9, 1988)     

Studies on the Growth in Culture of Plant Cells: XXI FINE STRUCTURAL FEATURES OF ACER PSEUDOPLATANULS L. CELLS RESPONDING TO 2,4-DICHLOROPHENOXYACETIC ACID WITHLDRAWAL IN TURBIDOSTAT CULTURE

A culture of Acer pseudoplatanus L. grown in the presence ofan equilibrium level of 2,4-dichlorophenoxyacetic acid (2,4-D)of 1?5 ? 10^–7 M (state IV culture) showed, in comparisonwith one of a similar specific growth rate but in which theequilibrium level of 2,4-D was 2?3 ? 10^–6 M (state Iculture), an enhanced degree of cell aggregation, enhanced meancell volume, and the presence of cells giving a generalizedlignin reaction with extracellular lignin-positive material.The state IV culture showed a proportion (10–15 per cent)of cells having ultrastructural features not observed in thestate I culture. Some of the cells, located at the surface ofthe cellular aggregates, were small, rounded, highly cytoplasmic,and rich in rough endoplasmic reticulum. Further within theaggregates there occurred some cells showing abnormal or incompletecytokinesis and having irregularly thickened walls. Locatedcentrally in the aggregates were cells showing massive accumulationsof electron-dense material and with cell walls showing bandsof thickening alternating with thinner wall regions traversedby plasmodesmata. The latter cells are interpreted as cellsshowing intense polyphenol metabolism and imperfect xylogenicdifferentiation.     

Structure of the organs of attachment of brachiolaria larvae of Stichaster australis (Verrill) and Coscinasterias calamaria (Gray) (Echinodermata: Asteroidea)

The structure of the brachiolar arms and adhesive disk of the brachiolaria larvae of Stichaster australis (Verrill) and Coscinasterias calamaria (Gray) was determined from light microscopy and from scanning and transmission electron microscopy. The structure of these organs was very similar in both species.The brachiolar arms are comprised of a stem region terminating in a crown of adhesive papillae which are made up of a variety of secretory cell types. Principal among these are elongated cells producing very electron-dense secretory particles, which are released at the free cell surface attached to cilia. Secretory particles appear to be important in temporary attachment of the brachiolar arms to the substratum. Ciliary sense cells, possibly used in the recognition of specific substrata are located at the tip of adhesive papillae.The adhesive disk is comprised of large cells packed with secretory droplets and elongated intracellular fibres. In the attached adhesive disk, secretory droplets are lost, having formed the cement that attaches the disk to the substratum. It appears that adhesive papillae lateral to the adhesive disk hold the disk in position close to the substratum during secretion and hardening of the cement. The intracellular fibres are the principal anchoring structures running from microvilli (locked into the attachment cement) on the surface of the disk to the underlying connective tissue of the attachment stalk.     

Accumulation of Heavy Metals in Cell Walls of Polygonum cuspidatum Roots from Metalliferous Habitats

The distribution and accumulation of Cu²⁺, Zn²⁺ and Cd²⁺ ionsin the roots of Polygonum cuspidatum, collected from metalliferousand non-metalliferous habitats, were examined. About 90% ofthe metal ions was located in the cell wall fraction of rootsof plants grown in either type of habitat. The metal-ion exchangecapacity of the cell walls is not specific to the plants frommetalliferous habitats, and there were no significant differencesamong plants from the various habitats. The capacity for Cu²⁺ions was greater than that for Zn²⁺ or Cd²⁺ ions. Cu²⁺ ionshave a high affinity for the cell wall and, thus, it appearsthat the cell wall is a barrier for the transportation of Cu²⁺into the cytoplasm. (Received March 10, 1988; Accepted March 17, 1989)     

The Structure and Cytochemistry of the Pistil of Sternbergia lutea (Amaryllidaceae)

Studies were carried out on structural and cytochemical aspectsof the pistil of Sternbergia lutea (L.) KerGawl. The stigmais of the wet papillate type; the papillae are unicellular andare arranged densely around the rim of a funnel-shaped stigma.The stigma exudate is limited and is confined to the bases ofthe papillae and the inner lining of the stigma. The papillaeare smooth in the distal part and are covered with intact cuticle-pelliclelining. The cuticle is disrupted at places towards the baseof the papillae releasing the exudate. The exudate is rich inpectins and other polysaccharides but poor in proteins and lipids.The papillae show dense cytoplasmic profiles with extensiveendoplasmic reticulum (ER), abundant mitochondria, polyribosomesand active dictyosomes. The style is hollow. The stylar cavityis surrounded by two to four layers of glandular cells. In theyoung pistil the canal is lined with a continuous cuticle, butin the mature pistil the cuticle becomes disrupted and the canalis filled with the secretion produced by the cells of the surroundingglandular tissue. Ultrastructurally, the cells of the glandulartissue are very similar to the stigmatic papillae. The innertangential wall of the cells bordering the canal is uniformlythicker than other walls. The secretion in the stylar canal,as well as the intercellular spaces of the glandular tissue,stain intensely for pectins and polysaccharides but poorly forproteins and lipids. Pollen tubes grow through the stylar canal.Structural and cytochemical details of the pistil of Sternbergiaare compared with other hollow-styled systems. Pistil, Sternbergia lutea (L.) Ker-Gawl., stigma and style, structure and cytochemistry     

STRUCTURE OF THE CEPHALIC TENTACLES OF SOME SPECIES OF PROSOBRANCH LIMPET (PATELLIDAE AND FISSURELLIDAE)

The morphology and ultrastructure of the cephalic tentaclesand eye (optic vesicle) of some patellid and a fissurellid limpetspecies are described. The epithelium of the tentacle bearsciliated cells which have neural connections suggesting a sensoryfunction. In patellid limpets the density of these cells variesbetween species, with the greatest density (18 ciliated tufts.100 µm^–2) being recorded in the territorial limpet,Patella cochlear. The surface of the tentacle of a fissurellidlimpet, Fissurella mutabilis, is papillate, which contrastswith the smooth surface of a patellid tentacle. Ciliated tuftsare borne at the tip of most papillae. Movement of the tentacleis controlled by longitudinal muscle and a radial muscle-collagentissue association, which function as a muscular hydrostat.The eye of a patellid consists of a simple open vesicle anda retina which is comprised of one type of cell. By contrastthe optic vesicle of a fissurellid contains a lens, enclosedby a cornea and a retina which is composed of two types of cell,pigmented and photoreceptive. The ultrastructural features ofthe cells resemble those described for other molluscan eyes. (Received 5 June 1989; accepted 16 August 1989)     

Changes of Cell Wall Composition and Polymer Size in Primary Roots of Cotton Seedlings Under High Salinity

The aim of this study was to investigate changes in cell wallchemical composition and polymer size in the root tip of intactcotton seedlings (Gossypium hirsutum L. cv. Acala SJ-2) grownin saline environments, in order to relate the interaction betweenhigh salinity and root growth to possible changes in cell wallmetabolism. Cotton seedlings were grown in modified Hoagland nutrient solutionwith various combinations of NaCl and CaCl₂. Cell walls werefractionated into four fractions (pectin, hemicellulose 1 and2, cellulose), and analysed for their total sugar content, neutralsugar composition and size of polysaccharides. At 1 mol m^–3Ca, 150 mol m^–3 NaCl resulted in a significant increasein the cell wall uronic acid content, but a reduction in cellulosecontent on a per unit dry weight basis. Supplemental Ca overcamethe inhibitory effect of high Na on cellulose content. The neutralsugar composition of the cell wall fractions showed no majorchanges caused by varied Na/Ca ratios. Determinations of polysaccharidepolymer size showed that high Na at 1 mol m^–3 Ca led toan increase in the amount of polysaccharides of intermediatemolecular size and a decrease in that of small size in the hemicellulose1 fraction, indicating a possible inhibition of polysaccharidedegradation by high Na. This change was not observed in the10 mol m^–3 Ca treatments. The results reveal a relationshipbetween the effects of high salinity on root growth and cellwall metabolism, particularly in regard to cellulose biosynthesis Key words: Gossypium hirsutum, salinity, root, cell wall     

Ultrastructure and Secretion of Extrafloral Nectaries of Plumeria rubra L.

Extrafloral nectaries situated on the adaxial side of the petiolebase are differentiated into a long head, comprising subepithelialground tissue surrounded by a layer of elongated palisade-likeepithelial cells and a short stalk from the nectary meristem.Many ultrastructural changes occur in epithelial and subepithelialcells of the nectary, from the young to secretory stages, suchas an increase in the amount of cytoplasm rich in mitochondriawith well developed cristae, rough endoplasmic reticulum (rER),smooth endoplasmic reticulum (sER) tubules and Golgi bodies.Plasmalemma invaginations with secretory vesicles occur longthe radial walls. Substantial amounts of secretory materialaccumulate in the gap between the radial walls and subcuticularspace, probably carried by the secretory vesicles from the cytoplasmat the secretory stage. Before cessation of secretion the cytoplasmbecomes vesiculated and the volume of the vacuome increases.At the post secretory stage, cytolytic processes and death ofcells occur. The subepithelial cells attain their maturity priorto epithelial cells. Histochemical localization reveals thepresence of lipids, proteins and insoluble polysaccharides withinthe epithelial cells and in the secretory material depositedin the subcuticular space as well as the gap between the radialwalls of the epithelial cells and outside the cuticle. Fine structure, nectary, Plumeria rubra, granulocrine secretion     

Glandular Trichomes of Fagonia L. (Zygophyllaceae) Species: Structure, Development and Secreted Materials

The glandular trichomes ofFagoniaconsist of one secretory celland a multicellular stalk, which develops by division, elongationand elevation of epidermal cells. The latter become seperatedfrom the mesophyll and a subepidermal chamber is formed. Thelength of the stalk, which differs in the various species orvarieties is determined by the number of cell divisions and/or the extent of cell elongation. Although the basic morphologyand development of the trichomes of the species and varietiesexamined are similar, two types of mature trichomes can be distinguished:one occurs in the two examined varieties ofF. mollisand thesecond inF. glutinosaandF. arabica. The secretory cells of thesecond type possess a very thick wall and bear a porous cupuleon their top. Histochemical tests revealed that the sticky substancesecreted by the secretory cells contains mainly polysaccharidesand lipophilic compounds. The secreted material exhibits autofluorescence.InF. mollisvar.hispidachanges in the amount and shape of thefluorescent material inside the secretory cell, during the courseof development, have been observed. The contribution of theglandular trichomes inFagoniaspecies to survival in hot desertconditions is discussed. Fagonia; glandular trichomes; subepidermal chamber; secreted material; adaptation to desert conditions; stalk; fluorescence     

The Floral Nectary ofDigitalis purpureaL., Structure and Nectar Secretion

The floral nectary of the foxglove (Digitalis purpureaL.), locatedat the base of the ovary, was examined by: scanning electronmicroscopy; quantitative bright-field microscopy via computer-aided3-D reconstruction from serial sections; morphometric procedures;transmission electron microscopy and measurement of nectar effluxunder different experimental conditions. Time-lapse video recordingvia a microscope with incident light clearly showed that thenectar escaped from the apertures of modified stomata. The volumeflux via individual stomatal apertures was 0.31±0.1 nlmin^-1; therefore only a fraction of the total number of stomataper nectary (115±8) would be sufficient to dischargethe amount of nectar reported in previous publications. Thestomatal apertures are continuous with intercellular spacestraversing the small-celled nectariferous tissue. The latteris vascularized only by phloem, whose termini consists of rowsof slender cells. These sieve-like cells are surrounded by moreor less isodiametrical sheath cells with dimensions similarto the secretory cells. Details of nectary functioning are basedon enhanced structural information, complementary data on nectardischarge after experimental manipulations and the nature ofthe effluence.Copyright 1998 Annals of Botany Company Digitalis purpureaL.; foxglove; floral nectary; (ultra-)structure; 3-D reconstruction; morphometry; nectar flow; time-lapse video recording.     

Rhizobium-stimulated Callose Formation in Clover Root Hairs and its Relation to Infection

Callose was detected in the cell walls of the tips of growingroot hairs of Trifolium species and the non-legume Phleum pratenseusing u.v. fluorescence of fresh material stained with 0·005%aniline blue. Inoculation of the roots with Rhizobium trifolii,R. leguminosarum, R. meliloti, and R. japonicum, or additionof 10^–7 and 10^–8 M indole-3-acetic acid (IAA) increasedtip callose formation. Most tip callose was formed at 12 °C, and amounts declinedprogressively at 18, 24, and 30 °C, with very little formedat 36 °C. Tip calloso usually became less and disappearedin individual root hairs as they aged. Callose which appeared prominently in the host cell walls atthe points of initiation of infection threads did not usuallydisappear as the hairs matured. There was little or no extensionof callose along the infection thread and none in the threadtip or in the cell nucleus. Presumptive regions of callose hadsimilar structure and electron density as root hair wall materialand were sometimes related to arrays of vesicles in the hostcytoplasm. The external surface of the hair wall bore smallpegs or papillae (0·1–0·2 µm) continuouswith the outer layer of the wall and possibly associated withattachment of bacteria. Bacteria were usually umboriate at thepoint of attachment and their polyphosphate granules were muchlarger near the root hair than at the distal end.     

The Development, Structure and Function of Dendroid Colleters in Psychotria kirkii Hiern (Rubiaceae)

The dendroid colleters of the leaf nodulated Rubiaceous shrubPsychotria kirkii Hiern. have been studied with respect to theirdevelopment, structure and function. The colleters, which arisefrom the adaxial surface of stipules of apical and lateral shoots,secrete a protein/carbohydrate mucilaginous substance in whichis maintained a colony of leaf nodule bacteria. The colletersare multicellular and multiseriate, consisting of a two to fourcell thick stalk from which radiate up to 70 elongate secretorybranch cells. Cuticle envelops both stalk and branch cells inearly developmental stages and as secretory activity increasesthis cuticle is largely lost in two different ways. The majorpart is forced off the branch cell surface through the passageof a largely carbohydrate component of the mucilage which surroundsthe colleters: a second method of cuticle loss involves thepassage from the cell of small electron-translucent bodies whichbecome coated with cuticle as they exit the cell. The mucilagein which the bacterial cells are found provides a vehicle wherebythe bacteria are able to enter the leaves, thus leading to theinitiation of leaf nodules. Psychotria kirkii Hiern., secretory dendroid colleters, symbiosis, ultrastructure, trichome development