Water Pathways in Leaves of Hedera helix L. and Tradescantia virginiana L.

Hydraulic conductances of leaf tissues of Hedera helix and Tradescantiavirginiana leaves were measured. It was found that water couldflow most easily through the veins, but that the cell wallsof at least the ventral epidermis were more efficient at resupplyingwater lost from the epidermal tissue than was the mesophyllat rehydrating itself. Vein and bundle-sheath extensions, whichare characteristic of mesomorphic leaves (e.g. T. virginiana),seem to be important in maintaining a close hydraulic connectionbetween the epidermis and the vascular tissue. In leaves notcontaining vein and bundle-sheath extensions, typically xeromorphicleaves (e.g. H. helix), there is not such a close connectionbetween the epidermis and vascular tissue. This was shown inexperiments involving the sudden application of a reduced pressurepotential to either the epidermis or the other tissues of leaves,and the measurement of transient stomatal opening.     

Distinct parameters are involved in controlling the number of rounds of cell division in each tissue during ascidian embryogenesis.

We counted cell numbers during embryogenesis of the ascidian, Halocynthia roretzi, every hour. Cell numbers were determined by counting the numbers of nuclei in squashed embryos. The cell number of a larva just after hatching was approximately 3000. Our study addresses the question of what factors control the number of rounds of cell division during development. Three kinds of egg fragments were prepared by cutting unfertilized eggs to alter the volume of cytoplasm and the amount of DNA. After the egg fragments were fertilized, the cell numbers were estimated at the hatching stage. The cell numbers of the resulting larvae differed from those of normal larvae. Precursor blastomeres of various tissues were then isolated from normal and manipulated embryos, and cultured as partial embryos. The cell numbers of the resulting partial embryos were counted to estimate the number of cell divisions in each larval tissue. The results suggested that the number of cell divisions is controlled by a distinct mechanism in each tissue. We propose that the number of rounds of cell division during ascidian embryogenesis is controlled by three mechanisms: the first depending on the volume of cytoplasm; the second on the nucleo-cytoplasmic ratio; and the third depending on neither of these parameters. J. Exp. Zool. 284:379-391, 1999.     

Amitosis and Endocytogenesis in the Fruit of Malus sylvestris

Cyto-histological investigations on the initiation and developmentof a non-pathogenic physiological ‘cork spot’ necrosisin the outer cortex of the fruit of Malus sylvestris Mill. ‘YorkImperial’ revealed two distinct aberrancies, namely, amitoticnuclear division and intracellular or endogenous proliferationswithout hyperplasia per se The incipient necrotic conditionbecomes evident internally about 3 weeks after fruit set asminute isolated, discoloured, amorphous spots of disorganizedruptured cells within otherwise healthy cortical tissue Thedisorganization continues slowly with adjoining cells becomingsimilarly necrotic After the lysis of the initial cork spotcells, about 1 month later, sporadic cellular changes occurin various healthy vacuolated cortical cells contiguous to andencompassing the necrotic tissues. The nuclei increase in sizeand volume as they assume distinctive positions in preparationfor amitotic nuclear divisions. The enlarged nucleus or macronucleus,containing one or several nucleoli, divides by a distinct cleavagedeveloping from a constriction perpendicular to its longitudinalaxis The division results in the amitotic formation of two daughtermicronuclei that usually become separated by the formation ofa cell wall. No evidence of cell plate formation was observedand the method of cell wall formation could not be determined.Repeated amitotic divisions of the micronuclei result in anintracellular or endocytogenetic proliferation of parenchymatouscells that are invariably confined within the original mothercell until its wall ruptures The endogenous proliferations arereleased into lacunae or intercellular spaces, eventually becomedisorganized, and disintegrate, with the accumulated residualincrements resulting in an overall ‘cork spot’ appearance. Malus sylvestris Mill., apple, amitosis, endocytogenesis, multinucleate cells, macronuclei, micronuclei     

Anatomical Changes Which Occur in Cuttings of Agathis australis (D. Don) Lindl 1. Wounding Responses

The basal and sub-basal regions in cuttings of Agathis australisundergo a complex series of anatomical changes. Many of theseare categorized as wound responses and include cell divisionsassociated with the cut base and the proliferation of tracheidsand phloem which arise in the interfascicular region about 4mm above the cut base. The vascular tissue arcs outwards anddownwards through the cortex. It may develop as isolated strandsonly a few cells wide or as sheets involving a number of cells.The precise pattern of vascular development appears to be determinedby its extent at the point of origin and by the presence ofobstacles such as primary and secondary resin canals which arelocated to the outside of the vascular bundles in the stem.Secondary resin canals are produced only in the rooting zonein cuttings that show extensive cell division. They arise schizogenouslyand do not form an interlinking network. Root primordia arise in the cortex at the end of isolated strandsof newly developed vascular tissue. Primordia never form inassociation with sheets of tracheids or after the convergenceof strands. In some cases virtually the entire sub-base is filledwith vascular tissue as a result of cell division and the differentiationof parenchymatous tissue. Root primordia never appear in thissituation. Agathis australis (D. Don) Lindl, kauri, cuttings, wound responses, vascular development, resin canals, root primordia, cellular differentiation     

Storage Organ Development in Radish (Raphanus sativus L.). 2. Effects of Growth Promoters on Cambial Activity in Cultured Roots, Decapitated Seedlings and Intact Plants

The radish varieties Cherry Belle and Long White Icicle wereused to investigate the role of the shoot and the effects ofsynthetic growth promoters in controlling cambial activity inthe seedling axis. Development was compared in excised roots, roots with hypocotylsattached and intact seedlings cultured aseptically on a nutrientmedium. No cambial divisions were seen in isolated radicleswhich had been cultured for ten days following excision butretention of hypocotyl tissue or the entire shoot resulted incambial activity and the production of secondary vascular tissues.Enriching the culture medium by raising the sucrose conantrationto 8% and including 10^–5 M indol-3yl acetic acid (IAA)5 x 10^–6 M 6-benzylaminopurine (BA) and 5 x 10^–4Minositol enhanced root thickening, increasing stele and xylemdiameters in roots cultured both with and without attached shoottissues. The effects of shoot tissues and enrichment of themedium were additive. The effects of auxin, cytokinin and gibberellin (gibberellicacid, GA²) were also studied on daxpitated seedlings. BA wasmuch more effective in inducing cell divisions in the hypocotylthan either IAA or GA supplied separately but a mixture of IAA+GAalso produced clearly defined arcs of cambial tissue. Littlesecondary tissue had been produced after seven days' treatment,and stelar enlargement was due to the development of a cambialzone and cell expansion in the primary tissues. Only minor differencesin response were observed between the two varieties. No stimulation of storage organ development occurred when auxin,cytokinin or inositol was inwrporated into the inorganic culturesolution in which plants of Cherry Belle were grown. Rnphanus sarivus, radish, storage organ, cambial activity, growth promoters, indol-3-ylacetic acid, 6-benzylaminopurine, gibberellic acid     

A Comparison of the Morphology and Anatomy of Seedling Leaves of Lolium multiflorum Lam. and L. perenne L.

A rapid technique has been developed for studying the morphologyand anatomy of leaves of forage grasses. It has been used tocompare the leaf dimensions, numbers of structural elements,tissue proportions, stomatal and unicellular hair counts, andmesophyll cell number and size in one variety of Lolium multiflorumLam. and L. perenne L. There were large differences betweenthese species in leaf dimensions, number of structural elements,and in stomatal and unicellular hair counts, but little differencein the relative proportion of different tissues and in cellsize.     

Morphogenesis in Yucca schidigera Roezl. Root Organ Cultures

Root development in suspension cultures of Yucca schidigerawas light-mediated. The green cultures consisted of roots, smalltissue aggregates and suspension cells. Roots possessed an apicalmeristem with a root cap, meristematic region and region ofdifferentiating tissues. Phloem, xylem vessels and tracheidsoccurred in discrete polyarch vascular bundles. Xylary wallthickening was reticulate, and endodermis and pericycle werepresent. Roots of intact Y. schidigera plants had a similardistribution of vascular tissues. Dark-grown cultures were cream-colouredand contained only lobed tissue aggregates and suspension cells. Yucca schidigera Roezl., tissue cultures, morphogenesis, root organ, light/dark     

Induction of a 'Periderm-like' Tissue in Excised Roots of the Fern Ophioglossum petiolatum Hook

Basal applications of plant growth regulators to excised rootsof Ophioglossum induce modifications in the outer cortical cells.Benzyladenine initiates periclinal divisions in these outercells producing a ‘periderm-like’ tissue while 2,4-Dcauses cell enlargement only. Walls of the outer cells of the‘periderm-like’ tissue are resistant to sulphuricacid and stain with Sudan IV and presumably are suberized.     

Development and Histochemistry of the Pistil of the Grape, Vitis vinifera

The development of the grape pistil is followed for a periodof 9 weeks from flower initiation to anthesis. Three phasesof pericarp differentiation are revealed: ring meristem formation;cell proliferation by anticlinal cell divisions; and a maturationphase characterized by periclinal cell division and differentiation.Both the stigma papillae and the transmitting tissue of thestyle originate by periclinal cell divisions. The receptivestigma is of the wet type and comprises many filamentous papillae,each composed of about 20 cells and covered by a loose cuticle.The stigma exudate shows similar cytochemical properties tothe material in the intercellular spaces of the transmittingtissue and is physically continuous with it. After pollinationand coincident with withering of the stigma, a single layerof stylar cells becomes suberized, forming a protective layerof cicatrix. Vitis vinifera, grape, pistil, development, histochemistry     

Somatic Embryogenesis in Cassava: The Anatomy and Morphology of the Regeneration Process

Anatomical and morphological studies demonstrated that somaticembryos developed similarly on mature seed and clonal leaf explantsof cassava (Manihot esculenta Crantz) cultured for 20–24d on Murashige and Skoog (MS2) basal medium supplemented with4.0 mg l^–1 2,4-D (Stage 1) before transfer to MS2 basalmedium supplemented with 0–01 mg l^–1 2,4-D and 0–1mg l^–1 6-benzylaminopurine (Stage II medium). Within 7d of inoculation onto Stage I medium, cell divisions occurredin the adaxial tissues of cotyledon-piece and leaf-lobe explants,and associated with this was the development of embryogeneticprotusions and ridges on the adaxial surface. Foliose structuresand somatic embryo initials developed from these tissues oncotyledon, embryonic axis and leaf-lobe explants and, when cultureswere transferred to Stage II medium, further somatic embryodevelopment occurred. Somatic embryos apparently originatedfrom groups of cells and were identified by the presence ofa closed root axis, a shoot axis and cotyledons of similar shapeand venation to those of zygotic embryos. Somatic embryos hadno vascular connection with parental cultures. Manihot esculenta, cassava, somatic embryogenesis, tissue culture, anatomy, morphology, morphogenesis     

Vascular Differentiation in the Shoot Apex of Matteuccia struthiopteris

Initial vascular differentiation is generally considered tooccur in procambium. In ferns, however, a provascular tissueimmediately subjacent to the promeristem has been suggestedas an initial stage within which the procambium is subsequentlyformed. In contrast to this interpretation, a zonation conceptapplied in ferns recognizes a promeristem consisting of severallayers of cells in which no differentiation takes place. Thisstudy demonstrates that the shoot apex of Matteuccia struthiopterishas one cell layer of promeristem. Immediately subjacent tothe promeristem is the provascular tissue surrounding a centralgroup of pith mother cells. The developmental continuity betweenthe provascular tissue and the mature vascular tissue, and betweenthe pith mother cells and the pith, through transitional stages,indicates that the initial differentiation of vascular tissueand pith takes place in this prestelar tissue. The continuityof vascular differentiation in the area confronting young leavesor incipient leaf positions is interrupted by the formationof leaf gap initials. Developing leaves thus begin to exertinfluence on the vascular system at the prestelar stage. Smallprotoxylem elements with helical cell wall thickening, and distinctiveprotophloem elements are present in the leaf traces, but endabruptly near the junction regions of leaf traces to the meristele.Copyright1994, 1999 Academic Press Initial vascular differentiation, provascular tissue, pith mother cells, shoot apex, Matteuccia struthiopteris     

Morphogenesis in Relation to Chromosomal Constitution in Long-term Plant Tissue Cultures

A number of strains of callus tissues derived from 1-mm root tips of the garden pea, Pisum sativum L., cultivated on a complex medium containing yeast extract and 2, 4-D for eight years, were tested periodically for their capacity to initiate roots. Chromosomal cytological analyses accompanied each test. It was found that during the prolonged period of subculture there was a progressive loss of organ-forming Capacity in all tissue strains. At the outset all callus tissues could be stimulated to form normal diploid roots. After several years of continuous subculture, some callus tissues formed normal tetraploid roots. Still later, these callus tissues lost completely the capacity to initiate roots. This loss was paralleled by increasing abnormalities in the chromosomal constitution, including higher chromosome numbers and greater frequency of aneuploidy. Early in subculture normal diploid and tetraploid divisions were present in the callus tissues. Later, higher polyploids at 8n and 16n were more frequent, as well as aneuploids around these numbers. Some tissue strains after prolonged cultivation showed a wide range of chromosome numbers at the higher ploidy levels but completely lacked diploid divisions. It is suggested that the loss in organ-forming capacity is correlated with the increase in abnormality of chromosomal constitution. Differentiation of certain characteristic cell types was unaffected by these changes.     

Structural Development and Respiratory Activity of the Funiculus During Bean Seed (Phaseolus vulgaris L.) Maturation

Changes in the structural organization of the funiculus of Phaseolusvulgaris were correlated with mitochondrial respiration rates,including both cytochrome and alternative pathway activitiesand seed weight during development of the seed. After fertilization,vascular elements are still differentiating within the funiculus.The central core of the funiculus consists mainly of procambialcells together with a few mature xylem and phloem elements.As the seed gradually matures, more vascular elements beginto appear. Procambial cells in the upper region of the funiculusadjacent to the pod differentiate and result in xylem and phloemappearing as a convoluted, intertwining network of strands.In the lower part of the funiculus adjacent to the seed, fewervascular elements are present and they organize into a smallbundle prior to entering the seed. The funiculus is fully developedat the cotyledon stage judging from the size of the funiculusand the organization of the vascular tissues. At the early maturationstage, the seed begins to enlarge in both size and weight. Correlatedwith development of the funiculus tissue is a gradual decreasein total rates of respiration. Inhibitor studies using potassiumcyanide and/or salicylhydroxamic acid show that the CN-insensitive,or alternative pathway is the predominant route of electrontransport in funiculus mitochondria during the early stagesof development. This pathway declines in activity with age whereuponcytochrome pathway activity accounts for all of the respirationby the time vascular tissues are mature and the seed is rapidlyexpanding.Copyright 1994, 1999 Academic Press Funiculus, vascular tissue, cytochrome, respiratory pathway, alternative respiratory pathway, Phaseolus vulgaris     

Leaf Ontogeny in Digitaria eriantha

The shoot apex consists of two layers, the dermatogen and thehypodermis. The leaf primordia arise through periclinal divisionswithin these two layers on the side of the apex. Further divisionsof the dermatogen push the little protuberance upward and togetherwith divisions the hypodermis add internal tissues of the youngleaf. When the median and lateral bundles of the primordia arisein Digitaria eriantha they are isolated from the vascular supplyof the rest of the plant. The median strand, the first to form,and the first order laterals form at the disc of insertion ofthe primordium. The other laterals form higher up in the primordium.These strands extend both acropetally and basipetally to linkwith the vascular supply of the rest of the plant. Digitaria eriantha, apical meristem, leaf primordium, vascular bundle, orange G, tannic acid, iron alum     

Turgor and Longitudinal Tissue 12Helianthus annuus

The quantitative relationship between turgor and the pressureexerted by the inner tissues (cortex, vascular tissue, and pith)on the peripheral cell walls (longitudinal tissue pressure)was investigated in hypocotyls of sunflower seedlings (Helianthusannuus L.) In etiolated hypocotyls cell turgor pressures, asmeasured with the pressure probe, were in the range 0·38to 0·55 MPa with an average of 0·48 MPa. In irradiatedhypocotyls turgor pressures varied from 0·40 to 0·57MPa with a, mean at 0·49 MPa. The pressure exerted bythe inner tissues on the outer walls was estimated by incubatingpeeled sections in a series of osmotic test solutions (polyethyleneglycol 8000). The length change was measured with a transducer.In both etiolated and irradiated hypocotyls an external osmoticpressure of 0·5 MPa was required to inhibit elongationof the inner tissues, i.e. the average cell turgor and the longitudinaltissue pressure are very similar quantities. The results indicatethat the turgor of the inner tissues is displaced to and borneby the thick, growth-limiting peripheral cell walls of the hypocotyl. Key words: Helianthus annuus, hypocotyl growth, tissue pressure, turgor pressure, wall stress     

The Morphology and Development of Cross Veins in the Leaves of Bread Wheat (Triticum aestivum L.)

In the leaves of bread wheat Triticum aestivum L. the longitudinalvascular bundles are linked by small transverse bundles Pairsof similar small vascular bundles also link the upper ends ofminor longitudinal bundles to their neighbours in a Y-shapedarrangement The cross-vein procambial strands arise from unexpanded cellsof one layer of the mesophyll tissue. Lines of these cells connectone longitudinal procambial strand to the next The procambialcells subsequently undergo two tangential divisions to producecells which differentiate to form the conducting and parenchymatouselements of the mature cross veins. Anomalous cross veins are sometimes found. possible modes oforigin of these anomalous cross veins are considered.     

Studies on the Development of the Air Pores and Air Chambers of Marchantia paleacea: 1. Light Microscopy

The ontogeny of the air pores and air chambers of Marchantiapaleacea begins with the schizogenous development of protodermalintercellular spaces of the initial apertures, and is completedwith the formation of the air pores and giant sub-epidermalair chambers bearing numerous photosynthetic filaments. Intercellularspace formation commences from the thallus surface and proceedsinwards to the first internal layer of cells. The cells amongwhich spaces develop do not originate from one mother cell.Spaces are formed only in the regions of the intersection ofthe anticlinal walls of three, four, or sometimes more successivederivatives of S₁, S₃ and S₄ segments of the apical cell, oneor two of which have been divided periclinally and the restanticlinally. Protodermal intercellular spaces appear in mostor all the corners of these cells, the anticlinal walls of whichexhibit an opposite disposition. The S₁, S₂, S₃ and S₄ segmentsare produced by definite divisions of a five-sided apical celland by a series of divisions give rise to initial cells of theinternal layers of the thallus and initial cells of the protodermaland sub-protodermal layers. The concept of a quiescent apicalcell cannot be accepted, since dividing apical cells have beenobserved, and the pattern of wall disposition of the thallusapex cannot be explained without the active participation ofthe apical cell. The air chambers are apparently of exogenous origin. They resultfrom the broadening of the bottom of the initial apertures bythe coordination of the rate of anticlinal divisions and growthof the protodermal and sub-protodermal cells surrounding theintercellular spaces of the initial apertures. The ontogenyof the pore rings starts at an advanced stage of air chamberformation not from a mother cell but from the cells which surroundthe closed entrance of the air chamber, by a shift of the planeof division from anticlinal to periclinal. Before the periclinaldivisions a new axis of growth perpendicular to the thallussurface is established in the mother cells of the pore. By a polarized growth into the air chamber followed by periclinaldivisions, the cells of the floor form initial cells of thephotosynthetic filaments. The latter divide again to form singleor branched photosynthetic filaments. Marchantia paleacea, air pore, air chamber     

Regeneration Around Wounds and the Control of Vascular Differentiation

The question which was the basis of this work was whether (a)vascular regeneration around wounds includes a replacement ofdamaged tissues or (b) only new vascular strands, which arenormally formed from the cambium, are diverted around wounds.It was found that in Coleus and Cucumis no connections are formedto damaged sieve tubes and vessels, so that their continuityaround wounds is not restored. Pisum plants were wounded underconditions in which growth could not be influenced and the areaof the xylem in cross-section was measured 1 month later. Thewounds, which damaged the vascular tissues, significantly increasedvascular differentiation, indicating the replacement of a longnon-functional region of damaged tissues. The results indicatethat in the intact plant vascular differentiation is controllednot only by stimuli from the leaves but also by the capacityof the mature vascular system to transport these stimuli.     

Reactivation of the Cambium in Aesculus hippocastanum L.: A Transmission Electron Microscope Study

Changes taking place during cambial reactivation in Aesculushippocastanum have been studied using transmission electronmicroscopy. Cytoplasmic activity in the form of vesicle productionby dictyosomes and endoplasmic reticulum, and coated vesicleformation at the plasmalemma, was observed in samples collectedin mid-Feb. The first cell divisions occurred 1 month later,in cells to the phloem side of the cambium, and were of twotypes: penclinal divisions producing new phloem precursors,and oblique anticlinal divisions in phloem mother cells formedat the end of the previous growing season producing putativecompanion cell/sieve element pairs. The fusiform initial wasidentified as the cell adjacent to the boundary-layer of parenchymacells and was the last cell to divide, 2 weeks after the firstdivisions in phloem precursors. For the next 4 weeks phloemcells only were produced The first new differentiating xylemelements were formed in the middle of Apr., following a surgein the rate of cell division by the initial aRd its derivativexylem mother cells. These were a mixture of developing fibresand vessel elements. Some of the boundary-layer cells were converteddirectly to vessel elements without any division taking place,while others were derived from daughter cells of the fusiforminitial produced following its reactivation. Aesculus hippocastanum L., cambium, dormancy, reactivation