Some ultrastructural observations on the nature of foliar abscission in Impatiens sultani

Summary Both scanning and transmission electron microscopes have been used to study the anatomy of the abscission zone of Impatiens sultani Hook. Evidence is presented to show that the fracture line follows the middle lamella in all the living cells of the abscission zone including those in the vascular traces. The separation of these cells is preceded by a breakdown of the middle lamellar region of the wall. The characteristics of this process vary in different cell types. Accompanying this breakdown is an enlargement of inner cortex cells mainly in a direction parallel to the axis of the petiole. It is suggested that this expansion of cells is necessary to produce the tensions which rupture the cuticle and xylem vessels prior to separation. The occurrence of transfer cells and tyloses in the abscission zone is also described and the physiological implications of their presence discussed.     

Spatial and temporal aspects of cell separation in the foliar abscission zones ofImpatiens sultani Hook

Summary The abscission of leaves fromImpatiens sultani Hook. occurs as the direct result of the weakening of a narrow band of cells running transversely across the base of the petiole. This loss of strength of the abscission zone is due to the breakdown of the central cell wall in two or three layers of cells. The process of wall degeneration is first visible 13 hours after the induction of abscission in a small group of cells found just below the concave groove on the adaxial side of the petiole. As the abscission zone gets progressively weaker the area of cells showing wall breakdown expands, spreading through the parenchyma to the lower side of the stele. The walls of the collenchyma and epidermis along the sides and base of the petiole and the central vascular tissues are the last to break down. Experiments in which the abscission zone was dissected into small pieces were undertaken to investigate whether cell wall hydrolysis was a contagious phenomenon, spreading from cell to cell by direct contact. The results of these investigations indicated that there was little requirement for cell to cell contact in either the temporal or spatial integration of cell wall breakdown.     

Induced Abscission Sites in Internodal Explants of Impatiens sultani: A New System for Studying Positional Control: with an Appendix: A Mathematical Model for Abscission Sites

Intemodes from Impatiens sultani shoots, explanted into sterileculture, often developed a transverse separation layer afterone to two weeks and the top then abscised from the bottom ofthe explant. Such abscission occurred more rapidly and in agreater proportion of explants when 00001 per cent auxin (IAA)was provided basally and when younger intemodes and shorterexplants were used. The distance of the separation layer fromthe base of the explant varied little with explant length, butincreased with the concentration of auxin applied basally. It seems that in this adventitious abscission the processesof positional definition and differentiation proceed withoutpause, whereas in normal abscission the position is definedearly in development but the final stage of differentiationof the separation layer is delayed until much later when theorgan senesces. To account for the results from the internodal explants andfrom surgical operations on shoots as well as for the characteristicposition of abscission sites of leaves and fruits, we suggestthat the position of abscission is controlled primarily by auxinacting as a morphogen: abscission sites occur at Y-junctionsjust above the base of the arm with the lower activity and auxinstatus, or in single axes above a region of higher auxin status.In both sites, the auxin concentration decreases in the apicaldirection. This hypothesis is supported by a mathematical model (see Appendix)of the interaction of diffusive and polar transport in controllingthe concentration gradient along intemodes with specified auxinconcentrations maintained basally. The model allows predictionsconcerning the site and timing of abscission which accord withobservations on intemodal explants. Impatiens sultani Hook., abscission, auxin, differentiation, diffusion coefficient, IAA, morphogen, polar transport coefficient, positional control, separation layer     

Effects of Applied IAA on the Position of Abscission Sites Induced in Wounded Explants from Impatiens sultani Internodes

Previous work established that if segments of Impatiens sultaniinternodes are explanted and incubated on a suitable medium,they tend to undergo abscission by a transverse separation layerthat differentiates a short distance above the explant base.The present study has shown that the position of the abscissionsite can be modified experimentally. When an explant was splitdown to midlength and auxin (IAA) was applied to the top ofone of the two arms, abscission often occurred at or near thebase of the other arm. Again, when IAA was applied to the explantlaterally midway along its length, abscission often occurredjust above the application point. These two modifications ofabscission sites had been predicted by a hypothesis statingthat separation layers tend to be positioned where auxin concentrationdecreases in the morphologically upward direction. Studies with[¹⁴C]IAA confirmed that the separation layers above the explantbase, and in the two experimentally modified sites, did indeedarise where the concentration decreased upwards. Also, woundingaltered the position of abscission in these explants in waysthat can be interpreted in terms of the above hypothesis coupledwith the destruction of auxin that occurs at wound surfaces.In this system, auxin is acting as a morphogen: its concentrationgradients provide positional information. Impatiens sullani Hook., abscission, auxin, IAA, morphogen, positional control, separation layer, wounding     

The Role of Basipetal Auxin Transport in the Positional Control of Abscission Sites Induced in Impatiens sultani Stem Explants

If segments of Impatiens sultani stem are explanted and incubated,separation layers often form across them and lead to abscission.To test the suggested role of auxin concentration in controllingthe position of abscission sites, explants were labelled byapplying [¹⁴C]IAA to the shoot tip 4 h prior to explanting;transport of auxin applied in this way seems to resemble thatof endogenous auxin. During subsequent incubation of explantsfor 20 h, basipetal transport resulted in ¹⁴C accumulating justabove the base of the explants (nearly 80 % in the bottom 4mm of 24 mm explants). In internodal explants that had beenwounded at explanting by incising one side so as to sever avascular bundle, and in nodal explants with the leaf removed,the ¹⁴C also accumulated just above the wound or node to abouttwice the concentration otherwise expected; this accumulationwas probably due to basipetal transport being impeded by vasculardiscontinuity at the wound or node. Accumulation just abovethe base, or above a wound or node, resulted in gradients of¹⁴C concentration (presumably reflecting endogenous auxin concentration)decreasing in the morphologically upward direction at each ofthese three positions where abscission sites tend to occur. Impatiens sultani, abscission, auxin, IAA, node, polarized transport, positional control, separation layer, wounding     

Abscission of Phaseolus and Impatiens Explants: Effects of Ionizing Radiation upon Endogenous Growth Regulators and de Novo Enzyme Synthesis

Stem-petiole explants from the lower pulvinus of the primary leaves of Phaseolus vulgaris L. cv. Red Kidney and from Impatiens sultani Hook cv. Scarlet Baby were exposed to varying dosages of γ-radiation. With bean, irradiation of 175 to 525 kiloroentgens (kR) significantly accelerated the onset of abscission with a maximum response at 175 to 280 kR. Higher dosages (beginning at 600-700 kR) usually prevented abscission. With Impatiens, 18 to 35 kR significantly accelerated both the onset of abscission and possibly the initial abscission rate; 350 kR cut the time to 100% abscission in half and substantially accelerated the initial abscission rate. Inhibition of abscission in Impatiens was not possible with the available dose rate (35 kR/hour).     

Auxin Concentrations in Nodes and Internodes ofImpatiens sultani

Greater concentrations of auxin at nodes than in internodes,resulting from some nodal barrier to basipetal transport, havelong been postulated as the cause of early differentiation ofinitially isolated xylem and cambium at the nodes. However,this study, using [¹⁴C] indole-3-acetic acid (IAA) applied apicallyand gas chromatography-mass spectrometry, found that in stemsofImpatiens sultanithe IAA concentrations (per unit f. wt) atnodes were similar to those in adjacent internodes, though alittle greater at nodes if expressed per unit length of stemand a little less per unit d. wt. By contrast, in decapitatedshoots and in stem explants of dicotyledons, loss of the apicalsource of basipetally flowing auxin can result in auxin drainagewith some auxin retention in the uppermost remaining nodes.When [¹⁴C]IAA was applied apically to shoots for 4 h and stemexplants were excised, the explants had no nodal accumulationinitially whereas comparable explants incubated for 20 h revealedsignificant nodal accumulation. If decapitation leads both tonodal auxin accumulation and to adventitious abscission justabove the node, this fits the hypothesis that abscission sitesare positioned where auxin concentration decreases locally inthe apical direction. Difficulties in quantifying nodal auxindynamics are discussed, and some crude estimates of metabolicrates and locations of the auxin are presented.Copyright 1999Annals of Botany Company Abscission, auxin,Impatiens sultani, indole-3-acetic acid, node.     

Comparative Histocytology of the Petiole and the Main Pulvinus in Mimosa pudica L.

In Mimosa pudica, the main pulvinus, which brings about leafmovements, presents unusual structural characteristics in comparisonwith the petiole. Peculiar cellular features which exist inthe cortex, epidermis, parenchyma and endodermal regions includethe shape of the cells, their disposition and the location ofthe organelles. The central cylinder of the petiole is surrounded only by afew parenchyma layers whereas the central cylinder of the pulvinusforms a narrow central core enclosed in numerous cortical parenchymalayers. The phloem of the pulvinus contains collenchymatouscells towards the outside and possesses companion cells withwall ingrowths; these phloem members do not exist in the petiole.Xylem and protoxylem parenchyma cells of the petiole possesswall ingrowths which do not occur in homologous cells of thepulvinus. Moreover the pith of the pulvinus is composed of smallfibriform elements similar to the xylem fibriform elements ofthe organ. The structures observed may facilitate exchanges between cellsin the petiole and in the pulvinus. The predominant functionsof the organs relative to lateral and longitudinal transferof nutrients and conduction of stimuli are discussed. Mimosa pudica L., sensitive plant, pulvinus, ultrastructure, conduction of stimuli, leaf movement     

An ultrastructural study of abscission zone cells with special reference to the mechanism of enzyme secretion

Summary The ultrastructural changes which occur during the foliar abscission ofImpatiens sultani Hook. andColeus blumei Benth. have been described. In both cases fracture of the separation zone results from a modification of the wall and cleavage along the line of the middle lamella. This process starts at the corners of the cells and in regions rich in plasmodesmata.During the period of wall breakdown, cellular integrity is maintained and the membrane degradation described by others was not observed. Plasmolysis studies confirmed that the separation zone cells retained their selective permeability characteristics until well after wall fracture. Quantitative data are presented to show that there is an increase in the frequency of rough endoplasmic reticulum, dictyosomes and dictyosome vesicles during the period when wall-hydrolyzing enzyme secretion is occurring. These changes are interpreted as reflecting an increase in demand for the secretory machinery of the endomembrane system. The possible involvement of plasmodesmata in this process is also discussed.     

The Anatomy of Fruit Abscission in Loganberries

Loganberry fruits abscise at the base of the receptacle, justdistal to the sepals. As the fruit ripens, all cells of theabscission zone expand. The central parenchyma cells, due totheir position, appear to be the driving force behind abscission.Their expansion causes early cell-separation within a superficialzone of small cells and rupture of the epidermis at the sepal/receptaclejunction without prior dissolution of cell walls. However, othercells within the abscission zone have their walls degraded,mostly in the region of the middle lamella, as ripening progresses. Xylem transfer cells are found in abundance in the vascularbundles supplying the sepals. The outward curve of these bundlesinto the sepals brings the transfer cells into close proximitywith the abscission zone. A comparison of their distributionin loganberries with that in raspberries (MacKenzie, 1979),which are closely related but abscise at a different site, suggeststhat transfer cells may be implicated in the abscission process. The inevitable structural weakness brought about by the paucityof vascular tissue in the abscission zone relative to the morerobust pedicel may also predispose this area to separation. Anatomy, abscission, loganberry, Rubus idaeus x R, ursinus, Mailing Sunberry, transfer cells structure, fruit     

ABSCISSION OF LEAVES AND LEAFLETS IN ACER NEGUNDO AND FRAXINUS AMERICANA

A comparative study of leaf and leaflet abscission in Acer negundo and Fraxinus americana was undertaken with special emphasis on leaflet abscission. Leaf fall in both species is accomplished by orderly, fragmentary abscission of leaflets followed by petiole abscission. Leaflet fall was presaged by differentiation of a separation layer at leaflet bases 10–15 days prior to leaflet fall, without an accompanying protective layer. Anatomical studies of petiole abscission revealed early differentiation of a protective layer followed by differentiation of a separation layer at petiole bases just prior to petiolar fall. Abscission at both sites was facilitated by cell division and dissolution of cell walls within separation layers.     

Auxin and gibberellin effects on cell growth and starch during abscission in cotton

An increase in starch content of cells in the abscission zone of the cotton explant appeared correlated with an increase in number of cells. A large increase in the number of cells in the abscission zone, concomitant with an increase in starch content, followed treatment with gibberellin as compared to auxin. In the final stages of abscission starch was hydrolyzed in the cells of the separation layer. Some starch remained after the petiole abscised.

A positive phloroglucinol-hydrochloric acid reaction in the cells of the petiole distal to the line of separation indicated the presence, not of lignin, but of soluble sugars and uronic acids. This reaction was especially intense following gibberellic acid treatment.

It was concluded that gibberellin in accelerating abscission leads to (1) an increase in cell number and starch content in the abscission zone, (2) the hydrolysis of starch in the separation layer just before abscission, and (3) the breakdown of polysaccharides and the release of soluble sugars and uronic acids. Auxin, an abscission retardant, either delays or prevents these events.

     

Perianth Abscission in Montbretia (Crocosmia x crocosmiiflora)

The anatomy, histochemistry, kinetics and hormonal regulationof perianth abscission in Crocosmia x crocosmiiflora (Montbretia)has been investigated. The abscission zone is anatomically welldefined, with cell divisions occurring in this region at anthesis.Abscission is first detectable 3 d after perianth opening, whenthe walls of a group of cells beneath the adaxial epidermisshow reduced staining with polyanion-specific stains, and adecline in penanth break strength also occurs. Abscission isachieved by cell wall breakage in thc abscission zone, whichprogresses eccentrically from the adaxial epidermis throughthe abscission zone, rather than the separation of intact cellsas occurs in flowers of dicotyledons. Experiments on detachedflowers suggest similarities in the hormonal regulation of abscissionin Crocosmia to that of dicotyledons, in that an ethylene promotion,and possibly an auxin inhibition, mechanism may exist in Crocosmia.Ovary expansion occurs throughout the development and senescenceof unpollinated flowers, but does not appear to be the solecause of wall breakage in the abscission zone. It is suggestedthat hormonally regulated wall hydrolases weaken the cell wallsin the abscission zone, and allow wall breakage and subsequentabscission to occur. Cdrocosmia x crocosmiiflora, Montbretia, anatomy, breakstrength, cell wall changes, histochemistry, flowers, monocotyledons, perianth, senescence, ethylene, auxin     

A HISTOCHEMICAL STUDY OF ABSCISSION LAYER FORMATION IN THE BEAN

In debladed bean petioles calcium and dry weight increased in the abscission zone during an induction period of 14 hr. Before the microscopic appearance of the abscission layer calcium decreased in the abscission zone and increased in the petiole. Dry matter began to decrease in both the abscission zone and the petiole 24 hr after deblading. The first visual change in the cells of the abscission zone was a swelling of the pectic materials of the cell walls. This was followed by breakdown of other cell wall components, i.e., non-cellulosic polysaccharides and cellulose. The cellulose of the cell walls adjacent and distal to the abscission layer was found to be altered; however, no lignin was present during abscission layer development. The alteration of pectic materials, coupled with breakdown of cell wall components, resulted in the collapse of cells of the abscission layer just prior to separation. Auxin delayed abscission and also delayed the initial increase in calcium, the movement of calcium from the abscission zone to the petiole, and the decrease in dry weight.     

Photoassimilate translocation in the petiole of Cyclamen and Primula is independent of lateral retrieval

Phloem translocation of photoassimilates between source andsink is considered to be linked with active retrieval of sugarsleaked to the vascular apoplast. This hypothesis was evaluatedby studying photo-assimilate movement in petioles of intactplants of Cyclamen persicum and Primula obconica in the presenceof inhibitors affecting sucrose retrieval (PCMBS, CCCP). Inhibitorsolutions were applied by rinsing locally isolated petiole bundlesor by injection into the petioe parenchyma. PCMBS and CCCP reduced[¹⁴C]sucrose retrieval from the petiole apoplast by the vascularcells and altered the distribution pattern of ¹⁴C-photoassimilateswithin the petiole tissues. However, these treatments did notaffect translocation through the petiole phloem. Evidence isprovided that the reagents were present in the vascular apoplastsurrounding the translocating phloem. It was concluded thatassimilate movement in the petiole of Cyclamen and Primula wasindependent of apoplastic retrieval. Key words: Cyclamen, Primula, phloem, transport, path, sucrose, retrieval     

Analysis of abscission responses to photodecomposition products of 1-naphthaleneacetic acid

This paper presents an analysis of abscission reponses of cottonexplants to (a) 1-naphthaneneacetic acid; (b) photodecompositionproducts of 1-naphthaleneacetic acid: 1-methylnaphthalene, 1-naphthaldehyde,1-naphthoic acid, naphthalene, and phthalic acid; and (c) arelated compound: naphthaleneacetyl aspartate. Abscission wasaccelerated by low amounts and retarded by high amounts of 1-naphthaleneaceticacid and 1-naphthoic acid. No significant effect on abscissionwas observed from 1- methylnaphthalene, 1-naphthaldehyde, orphthalic acid applied in amounts from 10^–8 to 10.0 µgper petiole; or with naphthalene from 10^–3 to 10.0µgper petiole. Naphthaleneacetyl aspartate had no effect at 5?10⁴to 5?10^–3 µg per petiole, but completely inhibitedabscission at 5 ? 10^–1 and 5.0 µg per petiole. Thedata are analyzed on part by a previously described mechanicalmethod for the determination of abscission indexes, and in partby a new method described herein, using a digital computer forthe analysis of the abscission time-course data. The resultshave significance to the understanding of the variability encounteredin fruit thinning by 1-naphthaleneacetic acid and related substances,and are discussed in relation to the known intermediate effectsof 1-naphthaleneacetic acid in fruit thinning. ¹Present address: Department of Biology, Univesity of California,Riverside, California 92502, U.S.A. (Received August 26, 1972; )     

Jasmonates promote abscission in bean petiole expiants: Its relationship to the metabolism of cell wall polysaccharides and cellulase activity

Jasmonic acid (JA) and its methyl ester (JA-Me) promoted the abscission of bean petiole expiants in the dark and light, and the activity of these compounds was almost same. JA and JA-Me did not enhance ethylene production in bean petiole expiants in the light, indicating that the abscission-promoting effects of these compounds are not the result of ethylene. Cells in the petiole adjacent to the abscission zone expanded during abscission but not in the pulvinus, and JA-Me promoted cell expansion in the petiole and the pulvinus. JA-Me had no effect on the total amounts of pectic and hemicellulosic polysaccharides in 2-mm segments of the abscission region, which included 1 mm of pulvinus and 1 mm of petiole from the abscission zone. On the other hand, the total amounts of cellulosic polysaccharides in this region were reduced significantly by the addition of JA-Me in the light. JA-Me had no effect on the neutral sugar composition of hemicellulosic polysaccharides during abscission. The decrease in the endogenous levels of UDP-sugars in the petiole adjacent to the abscission zone was accelerated during abscission by the addition of JA-Me in the light. Cellulase activities of pulvinus and petiole in 10-day-old seedlings were enhanced by the addition of JA. These results suggest that the promoting effect of JA or JA-Me on the abscission of bean petiole explants is due to the change of sugar metabolism in the abscission zone, in which the increase in cellulase activity involves the degradation of cell wall polysaccharides. Jasmonic acid (JA) and its methyl ester (JA-Me) are considered to be putative plant hormones for a number of reasons, including their wide occurrence in the plant kingdom, biologic, activities in multiple aspects at low concentrations, and their interaction with other plant hormones (for reviews see Parthier 1991, Hamberg and Gardner 1992, Sembdner and Parthier 1993, Ueda et al. 1994a). We have already reported that JA and JA-Me and C₁₈-unsaturated fatty acids, which are considered to be the substrates of the biosynthesis of jasmonates, are powerful senescence-promoting substances (Ueda et al. 1982b, 1991a). Senescence symptoms induced by these compounds are identical to those of natural senescence. Recently we have also found that JA inhibited indole-3-acetic acid (IAA)-induced elongation of oat (Avena sativa L. cv. Victory) coleoptile segments by inhibiting the synthesis of cell wall polysaccharides (Ueda et al. 1994b, 1995). These facts led us to study the mode of actions of JA and JA-Me on promoting abscission, which is considered the last dramatic phenomenon of senescence. In this paper we report that JA and JA-Me promote abscission in bean (Phaseolus vulgaris L. cv. Masterpiece) petiole expiants and that the changes in the metabolism of cell wall polysaccharides in the petiole and the pulvinus adjacent to the abscission zone are involved in the promotive effects of these compounds.Abbreviations ABA abscisic acid - ACC 1-aminocyclopropane-1-carboxylic acid - DCB 2,6-dichlorobenzonitrile - HPLC high performance liquid chromatography - IAA indole-3-acetic acid - JA jasmonic acid - JA-Me methyl jasmonate - MES 2-(N-morpholino)ethane-sulfonic acid, monohydrate - TCA trichloroacetic acid - Tris 2-amino-2-hydroxymethy-1,3-propanediole     

Leaf Abscission in Soybean: Cytochemical and Ultrastructural Changes following Benzylaminopurine Treatment

6-benzylaminopurine (BAP) delays leaf abscission of soybeanGlycine max (L.) Merr. Abscission of the distal pulvinus ofprimary leaves was induced in 12-d-old seedlings or explantsby removal of the leaf blade. BAP applied to the cut end ofthe pulvinus following leaf blade removal delayed abscission.Discoloration of the pulvinus occurred before abscission commencedand the number of grana in chloroplasts within cortical parenchymacells of the pulvinus decreased over time following leaf bladeremoval. BAP prevented discoloration of pulvinus tissues anda decrease in grana number. Starch grains within amyloplastsof cells of the starch sheath in the pulvinus disappeared followingleaf blade removal, whereas starch accumulated within the abscissionzone prior to abscission. BAP prevented this apparent redistributionof starch and instead promoted an increase in starch withinplastids of cortical parenchyma cells of the pulvinus. Duringthe abscission process, cells within the separation layer enlargedand their nuclei and nucleoli became more evident prior to theirseparation from one another. Cell separation resulted from breakdownof middle lamellae and partial degradation of primary cell walls.Cycloheximide applied directly to the external surface of theabscission zone inhibited abscission in a similar way to theBAP treatment. These results suggest that BAP prevents abscissionby altering patterns of starch distribution in the pulvinusand abscission zone and by inhibiting the synthesis of proteinsthat typically appear de novo in induced abscission zone tissues. Key words: Benzylaminopurine, BAP, Soybean, Pulvinus, Abscission, amyloplast.     

Short-term effects of cytokinins on the lipid fatty acids of green leaves

Isolated shoots of Coleus blumei and isolated leaves from thisspecies and from Impatiens sultani were fed zeatin for differentperiods. High doses of the hormone (100 µg/ml) causeda measurable effect on lipid fatty acid composition after atwo-hour feeding period in isolated leaves of Coleus. The maximumeffects were at 20–30 µg zeatin taken up per g freshweight. With the leaves of Impatiens, higher doses of the hormonewere needed to obtain optimal effects. In both species, theproportion of linolenic acid increased and that of palmiticacid decreased. For higher concentrations, the reverse was true.The effects of the hormone on the fatty acids of glycolipidswere more apparent than on those of phospholipids. The resultsare discussed in view of the general importance of dose-responsecurves for cytokinin effects and the possible effects on cellmembranes. (Received November 11, 1978; )     

Cellular pathway of photosynthate transport in coats of developing seed of Vicia faba L. and Phaseolus vulgaris L. II. Principal cellular site(s) of efflux

The cells responsible for the photosynthate efflux from coatsof developing seed of Vicia faba L. and Phaseolus vulgaris L.were elucidated using known properties of the efflux mechanism.Sensitivity of sucrose efflux to NEM and high potassium concentrationswas retained by seed-coat halves of Phaseolus following pectinaseremoval of the branch parenchyma cell layer. In contrast, removalof the thin-walled parenchyma transfer cell layer from Viciaseed-coat halves abolished this sensitivity. The membrane-impermeantthiol-binding fluorochrome, qBBr, selectively stained the surfaceof the thin-walled parenchyma transfer cells. This phenomenonwas inhibited by the slowly permeable sul-phydryl agent, PCMBS,indicating that the plasma membranes of these cells are enrichedin sulphydryl groups characteristic of membrance porter proteins.On the basis that carrier-mediated sucrose efflux from seedcoats appears to be proton coupled, the putative plasma membraneH+-ATPase was used as a marker for the cells responsible forcarrier-mediated photosynthate efflux. When seed-coat halveswere exposed briefly at pH 8.5 to the weak acid fluorochrome,SRG, the ground parenchyma and thin-walled parenchyma transfercell layers selectively accumulated the dye. The apparent lowpH environment in the walls of these cells that renders SRGmembrane permeant appeared to be maintained by a VAN-sensitiveproton pump. The findings with SRG were corroborated by thecyto-chemical localization of plasma membrane ATPase activityto the ground parenchyma and thin-walled parenchyma transfercells using precipitation of cerium phosphate. Together, ourobservations provide qualified support for the conclusion thatcarrier-mediated photosynthate efflux from coats of Phaseolusand Vicia seed is primarily restricted to the ground parenchymaand thin-walled parenchyma transfer cell layers, respectively. Key words: Ground parenchyma, Phaseolus vulgaris L., photosynthate efflux, seed coat, transfer cell, Vicia faba L.