Sucrose transport into the phloem of Ricinus communis L. seedlings as measured by the analysis of sieve-tube sap

Careful cutting of the hypocotyl of Ricinus communis L. seedlings led to the exudation of pure sieve-tube sap for 2–3 h. This offered the possibility of testing the phloem-loading system qualitatively and quantitatively by incubating the cotyledons with different solutes of various concentrations to determine whether or not these solutes were loaded into the sieve tubes. The concentration which was achieved by loading and the time course could also be documented. This study concentrated on the loading of sucrose because it is the major naturally translocated sieve-tube compound. The sucrose concentration of sieve-tube sap was approx. 300 mM when the cotyledons were buried in the endosperm. When the cotyledons were excised from the endosperm and incubated in buffer, the sucrose concentration decreased gradually to 80–100 mM. This sucrose level was maintained for several hours by starch breakdown. Incubation of the excised cotyledons in sucrose caused the sucrose concentration in the sieve tubes to rise from 80 to 400 mM, depending on the sucrose concentration in the medium. Thus the sucrose concentration in the sieve tubes could be manipulated over a wide range. The transfer of labelled sucrose to the sieve-tube sap took 10 min; full isotope equilibration was finally reached after 2 h. An increase of K⁺ in the medium or in the sieve tubes did not change the sucrose concentration in the sievetube sap. Similarly the experimentally induced change of sucrose concentration in the sieve tubes did not affect the K⁺ concentration in the exudate. High concentrations of K⁺, however, strongly reduced the flow rate of exudation. Similar results were obtained with Na⁺ (data not shown). The minimum translocation speed in the sieve tubes in vivo was calculated from the growth increment of the seedling to be 1.03 m·h^-1, a value, which on average was also obtained for the exudation system with the endosperm attached. This comparison of the in-vivo rate of phloem transport and the exudation rate from cut hypocotyls indicates that sink control of phloem transport in the seedlings of that particular age was small, if there was any at all, and that the results from the experimental exudation system were probably not falsified by removal of the sink tissues.Abbreviations PTS 3-hydroxy-5,8, 10-pyrenetrisulfonate     

Studies on the Movement of Solutes between the Sieve Tubes and Surrounding Tissues4: II. PATHWAYS OF ION TRANSPORT FROM THE XYLEM TO THE PHLOEM

It has been shown that the time lapse of 2–3 hours foundby Peel (1963), between the introduction of an inactive ioninto the xylem of a stem segment and its appearance in honeydewcollected from that segment, is not an artefact caused by detectionmethods. A delay of similar magnitude was found in the presentexperiments when radioactive rubidium, ³²P-phosphate, or ³⁵S-sulphatewas used. Pretreatment of stem segments with the respectiveinactive ion caused a very considerable increase (20 hours)in the time lapse when the radioactive ions were subsequentlysupplied to the segment. Experiments with bark strips demonstratedthat the time lapse was due to the presence of a barrier tothe radial movement of ions from the xylem of segments, sinceusing bark strips the time lapse was reduced to less than onehour. This barrier could either be the xylem itself, the cambium,or both tissues. Pretreatment of bark stnps with inactive ionsincreased the time lapse in the case of ³²P-phosphate and ³⁵Ssulphate, but had no detectable effect with radioactive rubidium.It is considered that these results indicate that rubidium maybe able to pass directly into the sieve tube from the bathingsolution in bark strips. Phosphate and sulphate, however, mayhave to move into the sieve tube via the storage cells of thebark. It has been shown that phosphorus-32 activity in the sievetube is not confined to inorganic phosphate, but is certainlypresent in other compounds of which three sugar phosphates havebeen identified.     

Stimulation of sugar loading into sieve elements of willow by potassium and sodium salts

Potassium as the chloride, nitrate or sulphate or sodium as the chloride, were applied at a concentration of 50 mM either to the xylem of stem segments or to the cambial surface of bark strips of willow. Potassium chloride increased the concentration of sucrose in sieve tube exudate collected via severed aphid stylets, without significantly affecting the volume flow rate, or the concentration of potassium in the exudate. The increase in the sucrose level in the sieve tube sap was shown to be due to a stimulation of loading, rather than to an enhancement of longitudinal transport. Potassium nitrate and sulphate or sodium chloride, were not as effective as potassium chloride in stimulating the loading of sucrose. It is suggested that uptake of the cation into cells supplying sugars to the sieve tube is linked to the rate of release of sugars by the supplying cells.     

Loading and source of sugars for the sieve elements in stems of willow

Uniformly labelled [¹⁴C]glucose was introduced into the xylem of segments of willow stem. Forty-eight hours later sieve-tube sucrose was collected via servered aphid stylets, and the distribution of radioactivity in the hexose moieties of this was compared with the distribution in those of sucrose extracted from the segment. Very little correlation was found between the two sets of values, indicating possible inversion during loading. This lack of correlation could not be attributed to contributions to the sieve-tube sucrose from pools of labelled hexoses in the segment. Further experiments, however, showed quite high degrees of correlation between sieve-tube sucrose and sucrose extracted from the wood, indicating that the latter tissue was a major source of sieve-tube sucrose. This conclusion was substantiated in experiments in which sieve-tube exudate, obtained from stem segments, was compared with exudate obtained from the isolated bark of the segment. In other experiments, stylets were established on stem segments, then on isolated pieces of bark obtained from these segments. Sucrose and potassium exudation rates fell by as much as 50% on removing the bark from the segment. It was not possible to formulate a precise figure for the contribution of the wood to stylet exudation owing to injury effects and the complexity of the experimental system. No firm evidence could be found in support of the view that sucrose is inverted during loading of sieve elements from the storage cells of the stem.     

The Movement of Ions from the Xylem Solution into the Sieve Tubes of Willow

Sieve-tube exudate was obtained as honeydew from colonies ofthe aphid, Tuberolachnus salignus (Gmelin), feeding on isolatedstem segments of willow. Potassium and sodium were shown tobe present in this honeydew. On perfusing the xylem with a solutionof potassium or sodium chloride, a considerable uptake of thecation took place. This uptake was followed, after a periodof several hours, by an increase in the concentration of theparticular cation in the honeydew. A relationship was shown to exist between the concentrationof these cations in a given segment and their concentrationin honeydew obtained from that segment. No such relationshipexisted, however, with different segments. These results arediscussed in relation to the factors which possibly controlthe movement of solutes into the sieve tube.     

The effect of low temperature on sucrose,ATP and potassium concentrations and fluxes in the sieve tubes of willow

Summary Experiments have been performed on the effect of localised low (0°C) temperature application on solute concentration and fluxes in the sieve elements of willow. Sieve tube exudate was obtained via the severed stylets of the aphid Tuberolachnus salignus (Gmelin). In stem segments, low temperature caused a fall in both the concentration and flux of sucrose. No recovery was observed during a 24 h cold application period. The concentrations of ATP and potassium were generally also reduced, though the effect on the fluxes of these solutes was not as marked. Both ATP and potassium appear to be translocated along the sieve tubes of stem segments as evidenced by girdling experiments. In leafy cuttings low temperature consistently reduced the concentration of sucrose in the sieve tube exudate. These data are discussed in relation to previous work on low temperature effects on the phloem transport system of willow.     

The Cellular Pathway of Short-distance Transfer of Photosynthates and Potassium in the Elongating Stem ofPhaseolus vulgarisL. A Physiological Assessment

Plasmolytic disruption of plasmodesmata interconnecting metaphloemsieve element-companion cell complexes with small and largephloem parenchyma cells in the elongating region of internode2 ofPhaseolus vulgarisL. seedlings did not affect accumulationof phloem-imported¹⁴C-photosynthates and⁸⁶rubidium. The membrane-impermeantdye, 5(6) carboxyfluorescein, loaded into leaf phloem as themembrane-permeant diacetate ester, was found not to move radiallyout of the importing sieve elements in the internode elongationregion. In contrast, the apoplasmic tracer, Calcuofluor White,rapidly moved laterally throughout all tissues of the elongationzone. Hexoses, sucrose and potassium were identified as themain osmotica in internode apoplasmic sap. Label asymmetry in[¹⁴C](fructosyl)sucrose was retained on accumulation by excisedstem segments. Uptake of [¹⁴C]sucrose and⁸⁶rubidium by stemsegments exhibited saturation kinetics. Sucrose uptake was inhibitedby the slowly penetrating sulphydryl reagent, para-chloromercuribenzenesulphonicacid.In vitrorates of sucrose uptake, at apoplasmic concentrations,corresponded to its predictedin vivorate of delivery to thestem ground tissues from mature sieve elements when respiratorylosses were assumed to be confined to the stem phloem. For potassium,the total delivery rate could be accounted for by itsin vitrorateof uptake. Overall, it was concluded that radial transport,in the elongation zone of internode 2 ofPhaseolus vulgarisL.seedlings, follows an apoplasmic route from mature sieve elementsto stem ground tissues.Copyright 1998 Annals of Botany Company PhaseoluLes vulgaris, apoplasm, elongating stem, French bean, photosynthates, potassium, radial transfer, symplasm.     

Mineral uptake and transport in xylem and phloem of the proteaceous tree,Banksia prionotes

Xylem sap of sinker (tap) root, cluster feeding roots, lateral roots and from an age series of main stem extensions of 6-year trees of Banksia prionotes was collected and analyzed for principal organic and inorganic solutes. During the phase of root uptake activity in winter and spring, cluster roots were principal xylem donors of malate, phosphate, chloride, sodium, potassium and amino acid N whereas other parts of the root served as major sources to the shoot of other cations, nitrate and sulphate. Sinker root xylem sap was at all times less concentrated in solutes than that of lateral roots into which cluster roots were voiding exported solutes. Phosphate was abstracted from xylem by stem tissue during winter and it and a range of other solutes released back to xylem immediately prior to extension growth of the shoot in summer. Phloem sap collected from mid regions of stems was unusually low in potassium and phosphate relative to chloride and sulphate in comparison with phloem sap of other species, and its low potassium: sodium ratio relative to xylem indicated poor discrimination against sodium during phloem loading. Data are discussed in relation to the asynchronous seasonal cycles of nutrient uptake and shoot growth.     

Aphid stylectomy reveals an osmotic step between sieve tube and cortical cells in barley roots

The aim of the present study was to quantify osmotic pressuresdirectly in the translocation pathway, from leaf to growingroot tip, in order to understand the forces driving solutesfrom a source to a sink. Solutes move through the translocationpathway down an osmotically derived turgor gradient. Accordinglyaphid stylectomy and single cell sampling techniques have beencombined to examine the osmotic pressure of root phloem andgrowing root cells. Sieve tube sap was obtained from shootsand, for the first time, roots of barley seedlings using aphidstylectomy. Vacuolar sap was also obtained from a variety ofcells in leaf and root tissues using single cell sampling methods.Osmotic pressure of sieve tube sap from roots and shoots wasmeasured at high temporal resolution (within min) and over longperiods of time (up to 24 h). Osmotic pressure did not changesignificantly in the minutes immediately following excision,suggesting that confidence can be placed in the assumption thatstylet exudate is representative of sieve tube sap in vivo.There were no differences in the osmotic pressure of sieve tubesap from shoots (1.240.26 MPa, n = 10) or roots (1.420.15MPa, n = 13). However, osmotic pressure of sap from root corticalcells (0.710.09, n = 12) was about 0.7 MPa lower than thatof the sieve elements from roots, this difference may be maintainedby consumption of incoming solutes at the root tip. Resultsare discussed in the context of pressure driven flow in thephloem and symplastic contact between root tip cells and sievetube. It is hoped that the approach described here will provideimportant insights into the nature of the relationship betweenroot cell extension and assimilate supply through the phloem. Key words: Phloem, sieve tube, aphid, root, barley, osmotic pressure, translocation     

Accumulation and Conversion of Sugars by Developing Wheat Grains : VI. Gradients Along the Transport Pathway from the Peduncle to the Endosperm Cavity during Grain Filling

Gradients along the transport pathway from the peduncle to the endosperm cavity were examined during grain filling in wheat. Sieve tube exudate was collected from severed aphid stylets established on the peduncle and rachis and on the vascular bundles in the creases of grains. Phloem exudate could also be collected from broken grain pedicels, and by puncturing the vascular bundle in the grain crease with a needle. Stylets on excised grains persisted exuding, indicating that grain sieve tubes are capable of loading solutes. There was little, if any, discernible gradient in osmolality or solute composition (sucrose, total amino acids) of sieve tube contents along the phloem pathway from the peduncle to the rachis or along the rachis itself. Neither was a gradient detected in osmolality along the sieve tube pathway from the rachis through the rachilla and grain stalk to the crease. Demonstrable solute gradients occurred only across those tissues of the grain crease between the crease sieve tubes and the endosperm cavity, a distance of just 1 millimeter. However, while the sucrose concentration in the sieve tubes was almost tenfold that in the endosperm cavity sap, total amino acids were only threefold higher, and the potassium concentrations of the two were equal. Our observations strongly implicate the movement of assimilates from the sieve tubes and across the crease tissues as important control points in grain filling.     

Tension in the Phloem?

The hydrostatic pressure in sieve tubes may probably be estimatedreasonably accurately from experimental measurements of theosmolarity of the sieve tube sap and of the tension in the xylem.The possibility of the existence of phloem tension is advanced.     

The Composition of Phloem Exudate and Xylem Sap from Tree Tobacco (Nicotiana glauca Grah.)

The composition of xylem sap and exudate from stem incisionsof Nicotiana glauca Grah. was compared in detail. Exudationfrom stem incisions occurred over a 5 min period in certainplants, enabling collection of 5–30 µl of sap. Therate of exudation showed an exponential decline. Exudate hada high dry matter content (170–196 mg ml^–1) andhigh sugar (sucrose) levels. Xylem sap had a low pH (5.8) andexudate a pH of 7.9. Glutamine dominated the amino compoundsin xylem sap and exudate, and K⁺ was the major cation. Totalamino compounds in stem exudate reached 10.8 mg ml^–1 whereasxylem sap contained much lower levels (0.28 mg ml^–1).All mineral elements and amino compounds with the exceptionof calcium were more concentrated in stem exudate than in xylemsap. Sucrose was labelled heavily in stem exudate following pulsingof an adjacent leaf with ¹⁴CO₂. A concentration gradient ofsugar (2.1 bar m^–1) was recorded for stems. Levels ofsucrose, amino compounds and K⁺ ions in stem exudate showeda diurnal periodicity. Each commodity reached maximum concentrationat or near noon and minimum concentration about dawn. The evidencesuggests that exudate from stem incisions of N. glauca is arepresentative sample of solutes translocated in the phloem. Nicotiana glauca Grah., phloem sap, xylem sap, sucrose, amino compounds, mineral ions     

Composition of Amino Compounds Transported in Xylem of Casuarina sp.

Seedlings (180-d-old) of Casuarina cunninghamianaM L., C. equisetifoliaMiq. and C. glauca Sieber inoculated with each of two differentsources of Frankia, were analysed for translocated nitrogenouscompounds in xylem sap. Analyses were also made on sap fromnodulated and non-nodulated plants of C. glauca grown with orwithout a range of levels of combined nitrogen. Xylem exudateswere collected from stems, roots, and individual nodules ofnodulated plants and from stems and roots of non-nodulated plants.While the proportional composition of solutes varied, the samerange of amino compounds was found in xylem sap from the threedifferent symbioses. In C. glauca asparagine was the major aminoacid in the root sap followed by proline, while in symbioticC. cunninghamiana arginine accounted for more than 25% of theamino compounds. Citrulline was the major translocated productfound in the stem exudate of symbiotic C. equisetifolia. Increasingconcentrations of ammonium nitrate in the nutrient solutionresulted in increasing levels of free ammonia and glutaminein xylem sap from stems of nodulated and non-nodulated C. glauca,but there was relatively little change in the prominent solutes,e.g. citrulline, proline, and arginine. The composition of nitrogenoussolutes in stem or root exudates of C. glauca was similar tothat of exudate collected from individual nodules and on thisbasis it was not possible to distinguish specific products ofcurrent N₂ fixation in xylem. The main differences in N solutecomposition between the symbioses were apparently due to hostplant effects rather than nodulation or the levels of combinedN. Also, the data indicate that the use of the proportion ofN in sap as citrulline (or indeed any other organic N solute)could not be used as an index of nitrogen fixation.     

Transport of organic solutes in Phloem and xylem of a nodulated legume

Collections of xylem exudate of root stumps or detached nodules, and of phloem bleeding sap from stems, petioles, and fruits were made from variously aged plants of Lupinus albus L. relying on nodules for their N supply. Sucrose was the major organic solute of phloem, asparagine, glutamine, serine, aspartic acid, valine, lysine, isoleucine, and leucine, the principal N solutes of both xylem and phloem. Xylem sap exhibited higher relative proportions of asparagine, glutamine and aspartic acid than phloem sap, but lower proportions of other amino acids. Phloem sap of petioles was less concentrated in asparagine and glutamine but richer in sucrose than was phloem sap of stem and fruit, suggesting that sucrose was unloaded from phloem and amides added to phloem as translocate passed through stems to sinks of the plant. Evidence was obtained of loading of histidine, lysine, threonine, serine, leucine and valine onto phloem of stems but the amounts involved were small compared with amides. Analyses of petiole phloem sap from different age groups of leaves indicated ontogenetic changes and effects of position on a shoot on relative rates of export of sucrose and N solutes. Diurnal fluctuations were demonstrated in relative rates of loading of sucrose and N solutes onto phloem of leaves. Daily variations in the ability of stem tissue to load N onto phloem streams were of lesser amplitude than, or out of phase with fluctuations in translocation of N from leaves. Data were related to recent information on C and N transport in the species.     

The differential transport of amino acids into the phloem of Ricinus communis L. seedlings as shown by the analysis of sieve-tube sap

The cotyledons of castor bean (Ricinus communis L.) act as absorption organs for amino acids, which are supplied to the medium. The analysis of the sieve-tube sap, which exudes from the cut hypocotyl, demonstrated the ability of the cotyledons to load particular amino acids into the phloem and to reject the loading of others. The sieve-tube sap of cotyledons, which were embedded in the endosperm, contained 150 mM amino acids, with 50 mM glutamine as the major amino acid, and 10–15 mM each of valine, isoleucine, lysine and arginine. Removal of the endosperm led to a drastic decline in the amino-acid content of sieve-tube sap down to 16 mM. Addition of single amino acid species to the medium increased the amino acid concentration in the sieve-tube sap in specific manner: glutamine caused the largest increase (up to 140 mM in exudate), glutamate and alanine smaller increases (up to 60 mM), and arginine the smallest. In addition, the amino acid composition of the sieve-tube sap changed, for instance, glutamine or alanine readily appeared in the sieve-tube sap upon incubation in glutamine or alanine, respectively, whereas glutamate was hardly discernible even in the case of incubation with glutamate; arginine was loaded into the sieve tubes only reluctantly. In general, glutamine and alanine accumulated four- to tenfold in the sieve tubes. The uptake of amino acids and of sucrose into the sieve tubes was interdependent: the loading of sucrose strongly reduced the amino acid concentration in the sieve-tube exudate and loading of amino acids decreased the sucrose concentration. Comparison of the concentrations of various amino acids on their way from the endosperm via the cotyledon-endosperm interface, through the cotyledons and into the sieve tubes showed that glutamine, valine, isoleucine and lysine are accumulated on this pathway, whereas glutamate and arginine are more concentrated in the cotyledons than in the sieve tubes. Obviously the phloem-loading system has a transport specificity different from that of the amino acid uptake system of the cotyledon in general and it strongly discriminates between amino acids within the cotyledons.     

Cellular Structures, Plasma Membrane Surface Areas and Plasmodesmatal Frequencies of the Stem of Phaseolus vulgaris L. in Relation to Radial Photosynthate Transfer

At an early stage of secondary development, the metaphloem sieveelements appeared to be the only functional axial transportconduit in fully elongated stems of P. vulgaris plants. Thereis no apparent barrier to the radial transfer of solutes inthe stem apoplast. However, radial transfer through the stemsymplast could be limited by discontinuities resulting fromprotoplast degeneration of the protophloem fibres and developingsecondary xylem fibres. Estimates of possible sucrose fluxesthrough the apoplastic and symplastic routes indicated thatradial photosynthate transfer from the sieve element-companioncell (se-cc) complexes of the stem metaphloem could follow eithercellular route. In the case of apoplastic transfer, the plasmamembrane surface area of the se-cc complexes is only sufficientto support some form of facilitated movement of sucrose. Incontrast, the plasma membrane surface area of the phloem parenchymais sufficient to permit passive diffusion of sucrose to theapoplast. Plasmodesmatal frequencies suggest that any symplastictransfer to the phloem parenchyma from the sieve elements wouldbe via the companion cells. Phaseolus vulgaris, french bean, stem, photosynthate, radial transfer (photosynthates), cellular pathway     

A Reanalysis of Particle Motion in Sieve Tubes of Heracleum

From an analysis of the Brownian motion of particles in sieveelements of Heracleum mantegazzianum and Heracleum sphondylium,Barclay and Johnson have suggested that the in situ viscosityof sieve tube sap is four to six times higher than has previouslybeen assumed. In particular, they obtained a value for the sapviscosity of about 10^–2 Pa s, which compares with a valueof 2 x 10^–3 Pa s for a 20 per cent (w/v) sucrose solution.The present paper describes a reanalysis of their data. It isargued that Barclay & Johnson underestimated the Brownianmotion of sieve element particles and so overestimated the sapviscosity. An exact correction was not possible, but it is concludedthat the in situ viscosity of Heracleum sieve tube sap mustbe less than 3 x 10^–3 Pa s, which corresponds to a sucroseconcentration of less than 29 per cent. Hence it may not beunreasonable to suppose that the viscosity of sieve tube sapis determined primarily by the concentration of sucrose, ashas been assumed in theoretical analyses of the Munch hypothesis.It is also concluded that the sieve tubes studied by Barclayand Johnson were not functional, in the sense that they didnot exhibit an axial bulk flow of sap. Heracleum, sieve tubes, Brownian motion, viscosity, Munch hypothesis     

The Physiology of the Sieve Tube: PRELIMINARY EXPERIMENTS USING APHID MOUTH PARTS

The willow aphid Tuberolachnus salignus feeds by inserting itsstylets into a single sieve element. If the insect is severedfrom its proboscis whilst feeding, sap from the sieve tube exudesfrom the cut end of the stylet canal and may continue for manyhours. By attaching a capillary tube the rate of exudation canbe measured and the sap analysed. Normally the rate of exudationwas about 1 mm.³ per h. This means a movement of water and sucroseof 100 cm./h. or 100 sieve elements per min. The sap was foundto contain between 5 and 15 per cent, sucrose, up to 0.4 percent, raffinose, no reducing sugars, and about 0.5 per cent,amino-acids. Girdles some distance above and below exuding stylets failedto stop exudation (Tables I and II). This indicates a rapidsealing of the cut ends of the sieve tube and a switch-overin source of supply from the leaves to storage cells in thestem. The use of isolated stem segments and even irrigated stripsof bark followed. Using these, the following points have beenestablished, (a) There is no polarity of movement (Table IV);(b) a minimal length of about 16 cm. of stem or 800–1,000sieve elements are needed to give the full exudation rate (Fig.5); (c) when the D.P.D. on the inside of the bark is raised(Figs. 6, 7, and 8), the rate of exudation declines, but theconcentration of the exudate rises and exudation continues,indicating a maintenance of turgor, even in face of a D.P.D.of 20 atm. or more. Secretion of sugar into the sieve tube continuesalbeit slowly even against a sieve tube concentration of 50per cent. These findings are discussed in relation to current theoriesof translocation and are considered to favour the mass flowhypothesis.     

The Contributory Length of Sieve Tubes in Isolated Segments of Willow, and the Effect on it of Low Temperatures

Using isolated stem segments in which a gradient of ³²P-phosphateactivity had been established, it has been demonstrated thatthe magnitude of the contributory length is much greater thanthe 16 cm previously measured by Weatherley et al. (1959). On cooling a portion of a stem segment between an aphid colonyand the high-activity end of a segment, a pattern of specificactivity changes were observed in collected honeydew which showthat the effect of cooling was to increase the magnitude ofthe contributory length. It is considered that this increaseprovides cogent evidence in favour of the concept that movementof solutes across the lateral wall of the sieve tube is directlyor indirectly dependent upon metabolic energy, whilst the longitudinalmovement down the sieve tube is not so dependent.     

Ultrastructural indications for coexistence of symplastic and apoplastic phloem loading in Commelina benghalensis leaves

The ultrastructural ontogeny of Commelina benghalensis minor-vein elements was followed. The mature minor vein has a restricted number of elements: a sheath of six to eight mestome cells encloses one xylem vessel, three to five vascular parenchyma cells, a companion cell, a thin-walled protophloem sieve-tube member and a thick-walled metaphloem sieve-tube member. The protophloem sieve-tube member (diameter 4–5 m; wall thickness 0.12 m) and the companion cell originated from a common mother cell. The metaphloem sieve-tube member (diameter 3 m; wall thickness 0.2 m) developed from the same precursor cell as the phloem parenchyma cells. Counting the plasmodesmatal frequencies demonstrated a symplastic continuum from mesophyll to the minor-vein phloem. The metaphloem sievetube member and the phloem parenchyma cells are the termini of this symplast. The protophloem sieve-tube member and companion cell constitute an insulated symplastic domain. The symplastic route, mesophyll to metaphloem sieve tube, appears to offer a path for symplastic loading; the protophloem sieve tube may be capable of accumulation from the apoplast. A similar two-way system of loading may exist in a number of plant families. Plasmodesmograms (a novel way to depict cell elements, plasmodesmatal frequencies and vein architecture) of some other species also displayed the anatomical requirements for two routes from mesophyll to sieve tube and indicate the potential coexistence of symplastic and apoplastic loading.