Measurement of turgor pressure and its gradient in the Phloem of oak

A direct method is described for measuring the pressure in secondary phloem sieve tubes of oak trees. One end of a 26-gauge stainless steel tube was shaped such that when it penetrated the outer bark and transected a few sieve elements, it was stopped by the xylem so that small openings in the end allowed phloem sap to enter the tube. The other end of the stainless tube (phloem needle) was joined to a long glass capillary sealed at its other end to form a manometer for measuring phloem sap pressure. A method for measuring the average osmotic and turgor pressures in cells of leaves is also described. Phloem turgor pressures varied greatly in a series of phloem punctures around the trunk at 1.5 and at 6.3 meters. The variation in turgor pressure was always greater than the variation in osmotic pressure. In a series of turgor pressures arranged in descending order, the values in a sequence for the upper level was usually a little (0-3 atm) larger than the values for the lower level. These results may suggest that translocation of assimilate is favored by a small turgor pressure gradient, but they do more to emphasize the complications in measuring gradients in an elastic low resistance distribution system composed of contiguous longitudinal conduits. The results also imply that the sieve tubes are inflated with assimilate fluid under high pressure which can readily move longitudinally and with less pressure drop than would be necessary if the sieve tubes were rigid.     

Linking phloem function to structure: Analysis with a coupled xylem-phloem transport model

We carried out a theoretical analysis of phloem transport based on Münch hypothesis by developing a coupled xylem-phloem transport model. Results showed that the maximum sugar transport rate of the phloem was limited by solution viscosity and that transport requirements were strongly affected by prevailing xylem water potential. The minimum number of xylem and phloem conduits required to sustain transpiration and assimilation, respectively, were calculated. At its maximum sugar transport rate, the phloem functioned with a high turgor pressure difference between the sugar sources and sinks but the turgor pressure difference was reduced if additional parallel conduits were added or solute relays were introduced. Solute relays were shown to decrease the number of parallel sieve tubes needed for phloem transport, leading to a more uniform turgor pressure and allowing faster information transmission within the phloem. Because xylem water potential affected both xylem and phloem transport, the conductance of the two systems was found to be coupled such that large structural investments in the xylem reduced the need for investment in the phloem and vice versa.     

Water Flow Across the Sieve-Tube Boundary: Estimating Turgor and Some Implications for Phloem Loading and Unloading. III. Phloem in the Leaf

The theory described in Part I of this series is applied hereto the loading of water and sucrose into the sieve-element-companion-cell(se-cc) complexes of minor veins. It is concluded that symplasticphloem loading cannot account for large increases in osmoticpressure from mesophyll to se-cc complex or the dilution ofsieve tube sap which is evident in leaves. By contrast, loadingfrom the free space into a symplastically isolated se-cc complexcan account for both these observations. Within the se-cc complex,sucrose and water will be transported from the companion cellsto the sieve elements by a pressure-driven flow of solutionthrough the cytoplasmic annuli of plasmodesmata. The associatedchanges in turgor and osmotic pressure are small, and so these-cc complex can be regarded as a single compartment with respectto water potential. The assumption that this compartment isat water flux equilibrium will lead to significant overestimatesof turgor gradients. However, if the trans-membrane water potentialdifference and the external water potential are taken into account,the correlation of such gradients with sieve-element dimensionsand / or transport velocities provides one means of testingthe Munch hypothesis of phloem transport Phloem, turgor, osmotic pressure, plasmodesmata, Münch hypothesis, Phloem loading     

Direct and indirect measurements of Phloem turgor pressure in white ash

Direct determinations and indirect calculations of phloem turgor pressure were compared in white ash (Fraxinus americana L.). Direct measurements of trunk phloem turgor were made using a modified Hammel-type phloem needle connected to a pressure transducer. Turgor at the site of the direct measurements was calculated from the osmotic potential of the phloem sap and from the water potential of the xylem. It was assumed that the water potentials of the phloem and xylem were close to equilibrium at any one trunk location, at least under certain conditions. The water potential of the xylem was determined from the osmotic potential of xylem sap and from the xylem tension of previously bagged leaves, measured with a pressure chamber. The xylem tension of bagged leaves on a branch adjacent to the site of the direct measurements was considered equivalent to the xylem tension of the trunk at that point. While both the direct and indirect measurements of phloem turgor showed clear diurnal changes, the directly measured pressures were consistently lower than the calculated values. It is not clear at present whether the discrepancy between the two values lies primarily in the calculated or in the measured pressures, and thus, the results from both methods as described here must be regarded as estimates of true phloem turgor.     

Water Flow Across the Sieve-Tube Boundary: Estimating Turgor and Some Implications for Phloem Loading and Unloading. II. Phloem in the Stem

Confirming a previous analysis by Lang (1974), it is concludedthat in tree trunks, phloem turgor and turgor gradients maybe estimated from osmotic pressure and osmotic-pressure gradients,respectively. The present analysis is an improvement becauseit is based on observed osmotic-pressure gradients rather thansupposed turgor gradients, and allowance is made for sucroseunloading and gradients of external water potential. It is concludedthat the rate of sucrose unloading in tree trunks must be lessthan 50 nmol m^–2 S m^–1. In small plants, higherrates of unloading (100 nmol m m^–2 S m^–1) and steeperconcentration gradients will lead to larger errors, but turgorpressures can still be estimated with acceptable accuracy. Oneshould be more cautious when considering turgor gradients insmall plants, although it seems likely that reasonable estimateswill still be obtained. Assuming plasmodesmatal transport throughan unconstricted cytoplasmic annulus, it is concluded that thesieve elements and their associated cells will sustain verysimilar turgor and osmotic pressures. Convection and diffusioncan both contribute significantly to plasmodesmatal sucroseunloading. Similarly, the plasmodesmatal volume flux will reflecta combination of pressure flow and osmosis. Water fluxes acrossthe sieve element plasmalemma and through the plasmodesmatacan be in opposite directions. It may be possible to assessthe extent of hydraulic coupling between the sieve elementsand their associated cells from studies of phloem water relations Phloem, turgor, osmotic pressure, plasmodesmata, phloem unloading, Munch hypothesis     

Gradients and dynamics of inner bark and needle osmotic potentials in Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies L. Karst)

Preconditions of phloem transport in conifers are relatively unknown. We studied the variation of needle and inner bark axial osmotic gradients and xylem water potential in Scots pine and Norway spruce by measuring needle and inner bark osmolality in saplings and mature trees over several periods within a growing season. The needle and inner bark osmolality was strongly related to xylem water potential in all studied trees. Sugar concentrations were measured in Scots pine, and they had similar dynamics to inner bark osmolality. The sucrose quantity remained fairly constant over time and position, whereas the other sugars exhibited a larger change with time and position. A small osmotic gradient existed from branch to stem base under pre‐dawn conditions, and the osmotic gradient between upper stem and stem base was close to zero. The turgor in branches was significantly driven by xylem water potential, and the turgor loss point in branches was relatively close to daily minimum needle water potentials typically reported for Scots pine. Our results imply that xylem water potential considerably impacts the turgor pressure gradient driving phloem transport and that gravitation has a relatively large role in phloem transport in the stems of mature Scots pine trees.     

Turgor-dependent unloading of assimilates from coats of developing legume seed. Assessment of the significance of the phenomenon in the whole plant

The in vivo significance of turgor-dependent unloading was evaluated by examining assimilate transport to and within intact developing seeds of Phaseolus vulgaris (cv. Redland Pioneer) and Vicia faba (cv. Coles Prolific). The osmotic potentials of the seed apoplast were low. As a result, the osmotic gradients to the seed coat symplast were relatively small (i.e. 0.1 to 0.3 MPa). Sap concentrations of sucrose and potassium in the seed apoplast and coat symplast accounted for some 45 to 60% of the osmotic potentials of these compartments. Estimated turnover times of potassium and sucrose in the seed apoplast of < 1 h were some 5 to 13 times faster than the respective turnover times in the coat symplast pools. The small osmotic gradient between the seed apoplast and coat symplast combined with the relatively rapid turnover of solutes in the apoplast pool, confers the potential for a small change in assimilate uptake by the cotyledons to be rapidly translated into an amplified shift in the cell turgor of the seed coat. Observed adjustments in the osmotic potentials of solutions infused between the coat and cotyledons of intact seed were consistent with the in vivo operation of turgor-dependent unloading of solutes from the coat. Homeostatic regulation of turgor-dependent unloading was indicated by the maintenance of apoplast osmotic potentials of intact seeds when assimilate balance was manipulated by partial defoliation or elevating pod temperature. In contrast, osmotic potentials of the coat symplast adjusted upward to new steady values over a 2 to 4 h period. The resultant downward shift in coat cell turgor could serve to integrate phloem import into the seed coat with the new rates of efflux to the seed apoplast. Circumstantial evidence for this linkage was suggested by the approximate coincidence of the turgor changes with those in stem levels of ³²P used to monitor phloem transport. The results obtained provide qualified support for the in vivo operation of a turgor homeostat mechanism. It is proposed that the homeostat functions to integrate assimilate demand by the cotyledons with efflux from and phloem import into the coats of developing legume seed.     

Potassium in the Apoplast of the Root Sink Region

Using carboxyfluorescein, a fluorochrome transported along the phloem, we demonstrated that symplasmic phloem unloading in the watermelon root occurred in the basal zone of the meristem adjusting to the elongation zone. In the similar zones of maize and pumpkin roots, a high level of potassium was detected by X-ray microanalysis in the cell walls and intercellular spaces. Potassium concentration in these compartments comprised two-thirds of that in the cytoplasm. Such proportion between potassium concentrations in the cytoplasm and apoplast was characteristic of both the cortex and stele. Since potassium is a dominant osmotically active component in root tissues, such a proportion between its intracellular and apoplastic concentrations provides for a low turgor pressure in the cells of the sink region, in the phloem in particular. This might increase a turgor pressure gradient along the translocation route between source and sink tissues, which is a driving force for phloem assimilate transport.__________Translated from Fiziologiya Rastenii, Vol. 52, No. 4, 2005, pp. 591–599.Original Russian Text Copyright © 2005 by Krasavina, Burmistrova, Feshchenko, Nosov.     

How to become a tree without wood – biomechanical analysis of the stem of Carica papaya L

Carica papaya L. does not contain wood, according to the botanical definition of wood as lignified secondary xylem. Despite its parenchymatous secondary xylem, these plants are able to grow up to 10‐m high. This is surprising, as wooden structural elements are the ubiquitous strategy for supporting height growth in plants. Proposed possible alternative principles to explain the compensation for lack of wood in C. papaya are turgor pressure of the parenchyma, lignified phloem fibres in the bark, or a combination of the two. Interestingly, lignified tissue comprises only 5–8% of the entire stem mass. Furthermore, the phloem fibres do not form a compact tube enclosing the xylem, but instead form a mesh tubular structure. To investigate the mechanism of papaya's unusually high mechanical strength, a set of mechanical measurements were undertaken on whole stems and tissue sections of secondary phloem and xylem. The structural Young's modulus of mature stems reached 2.5 GPa. Since this is low compared to woody plants, the flexural rigidity of papaya stem construction may mainly be based on a higher second moment of inertia. Additionally, stem turgor pressure was determined indirectly by immersing specimens in sucrose solutions of different osmolalities, followed by mechanical tests; turgor pressure was between 0.82 and 1.25 MPa, indicating that turgor is essential for flexural rigidity of the entire stem.     

Phloem water relations and translocation

Satisfactory measurements of phloem water potential of trees can be obtained with the Richards and Ogata psychrometer and the vapor equilibration techniques, although corrections for loss of dry weight and for heating by respiration are required for the vapor equilibrium values. The psychrometer technique is the more satisfactory of the 2 because it requires less time for equilibration, less tissue, and less handling of tissue. Phloem water potential of a yellow-poplar tree followed a diurnal pattern quite similar to that of leaves, except that the values were higher (less negative) and changed less than in the leaves.

The psychrometer technique permits a different approach to the study of translocation in trees. Measurements of water potential of phloem discs followed by freezing of samples and determination of osmotic potential allows estimation of turgor pressure in various parts of trees as the difference between osmotic potential and total water potential. This technique was used in evaluating gradients in water potential, osmotic potential, and turgor pressure in red maple trees. The expected gradients in osmotic potential were observed in the phloem, osmotic potential of the cell sap increasing (sap becoming more dilute) down the trunk. However, values of water potential were such that a gradient in turgor pressure apparently did not exist at a time when rate of translocation was expected to be high. These results do not support the mass flow theory of translocation favored by many workers.

     

Scaling phloem transport: information transmission

Sieve tubes are primarily responsible for the movement of solutes over long distances, but they also conduct information about the osmotic state of the system. Using a previously developed dimensionless model of phloem transport, the mechanism behind the sieve tube's capacity to rapidly transmit pressure/concentration waves in response to local changes in either membrane solute exchange or the magnitude and axial gradient of apoplastic water potential is demonstrated. These wave fronts can move several orders of magnitude faster than the solution itself when the sieve tube's axial pressure drop is relatively small. Unlike the axial concentration drop, the axial pressure drop at steady state is independent of the apoplastic water potential gradient. As such, the regulation of whole‐sieve tube turgor could play a vital role in controlling membrane solute exchange throughout the translocation pathway, making turgor a reliable source of information for communicating change in system state.     

Manometric Measurement of Turgor Pressures in Laticiferous Phloem Tissues2

A manometric technique for the determination of turgor pressuresin laticiferous phloem tissues has given reproducible resultsin Hevea brasiliensis and a few other tree species. In Hevea,early morning pressures are in the range 7.9–15.0 atmospheres,falling during the day and recovering at night. These diurnalpressure changes are positively correlated with atmosphericrelative humidity and negatively correlated with changes intemperature, evaporation, leaf water deficit, and stomatal opening.They are not displayed by trees devoid of leaves. Thus the lossin turgor is probably the result of withdrawal of water fromthe phloem tissues under transpirational stress. Pressures at the base of the trunk normally exceed those atthe top, the gradient usually approximating to 1 atmosphere/10metres at night and rising up to six times this figure duringthe day. This increase probably reflects the development oftension gradients in the xylem during transpiration. A generalturgor gradient from base to crown does not preclude mass flowin sieve-tubes in the opposite direction provided that ratesof loading and unloading are such that a sufficient osmoticgradient is maintained in them in the required direction. No marked long-term effects of regular tapping on turgor pressurehave been noted in Hevea trees and there is no evidence forseasonal changes in turgor under our conditions.     

Sieve element unloading: cellular pathway, mechanism and control

The transport and distribution of phloem – mobile solutes is predominantly determined by transport processes located at the sink end of the source – transport – sink system. Transport across the sieve element boundary, sieve element unloading, is the first of a series of sink transport processes. Unloading of solutes from the sieve elements may follow an apo- or symplastic route. It is speculated that the unloading pathway is integrated with sink function and that apoplastic unloading is restricted to situations in which movement through the symplast is not compatible with sink function. These situations include axial transport and storage of osmotically active solutes against concentration and turgor gradients between the sieve elements and sink cells. Coupled with alteration in sink function, the cellular pathway of unloading can switch in stems and possibly other sinks. Experimental systems and approaches used to elucidate the mechanism of sieve element unloading are reviewed. Unloading fluxes to the apoplast can largely be accounted for by membrane diffusion in axial sinks. However, the higher fluxes in storage sinks suggests dependence on some form of facilitated transport. Proton sucrose symport is assessed to be a possible mechanism for facilitated efflux of solutes across the sieve element plasma membrane to the sink apoplast. Unloading through the symplast may occur by diffusion or mass flow. The latter mechanism serves to dissipate phloem water and hence prevent the potential elevation of sieve element turgor that would otherwise slow phloem import into the sink. The possibility of energised plasmodesmatal transport is raised. Sieve element unloading must be integrated with subsequent compartmentation and metabolism of the unloaded solute. Solute levels are an obvious basis for control of sieve element unloading, but are found to offer limited scope for a mass action mechanism. Apoplastic, cellular pathway, sieve element, solute transport, symplastic. Translated into a turgor signal, solute levels could regulate the rate of unloading, metabolism and compartmentation forming part of a turgor homeostat irrespective of the pathway of unloading.     

Water Flow Across the Sieve-Tube Boundary: Estimating Turgor and Some Implications For Phloem Loading and Unloading. I. Theory

A mathematical model of water and sucrose transport across thesieve tube boundary is presented, based on conservation of matterand the phenomenological equations for plasmodesmatal transportbetween the sieve elements and their associated cells. Plasmodesmataltransport coefficients are discussed. In parts II–IV,the equations developed here are used to assess: (i) the estimationof phloem turgor gradients from osmotic pressure gradients;(ii) plasmodesmatal transport of water and sucrose between thesieve elements and adjacent cells; and (iii) the plausibilityof symplastic and apoplastic phloem loading and unloading insome primary sources and sinks. A list of symbols is given inAppendix 1 of this paper Phloem, turgor, osmotic pressure, loading, unloading, plasmodesmata, Munch hypothesis     

Direct evidence for pressure-generated closure of plasmodesmata

Pressure differentials were generated between adjacent leaf trichome cells of Nicotiana clevelandii using a modified micropressure probe/injection system. The location of the pressure differentials was altered using two main treatments: (a) puncturing one of the cells in the trichome to induce a large differential at its junction with the next basal cell, or (b) raising the pressure of the impaled cell and ‘clamping’ it at a higher value, thus creating a differential at its upper, as well as lower, wall. In both treatments basipetal intercellular transport of Lucifer yellow was impeded exactly at the sites predicted by the generated pressure differentials; at the base of punctured cells and at the top of clamped cells. In flaccid trichomes puncturing was without effect because the turgor of all the cells in the trichome was too low (<50 kPa) to generate a sufficiently large pressure differential between the punctured cell and its neighbours. Elevations of cell turgor (ΔP) in excess of 200 kPa or more were required to impede intercellular transport When cells were clamped at a high pressure and then subsequently allowed to lose their turgor by withdrawal of the probe the effects of the original pressure clamp were partially retained, indicating an inability to resume intercellular transport.     

Generalized Münch coupling between sugar and water fluxes for modelling carbon allocation as affected by water status

A model of within-plant carbon allocation is proposed which makes a generalized use of the Münch mechanism to integrate carbon and water functions and their involvement in growth limitations. The plant is envisioned as a branched network of resistive pathways (phloem and xylem) with nodal organs acting as sources and sinks for sucrose. Four elementary organs (leaf, stem, fruit, root) are described with their particular sink functions and hydraulic attributes. Given the rates of photosynthesis and transpiration and the hydraulic properties of the network as inputs, the model calculates the internal fluxes of water and sucrose. Xylem water potential (Psi), phloem sucrose concentration (C) and turgor pressure (P) are calculated everywhere in the network accounting for osmotic equilibrium between apoplasm and symplasm and coupled functioning of xylem and phloem. The fluxes of phloem and xylem saps are driven by the gradients of P and Psi, respectively. The fruit growth rate is assumed as turgor pressure dependent. To demonstrate its ability to address within-plant competition, the model is run with a simple-branched structure gathering three leaves, eight stem segments, three competing growing fruits and one root. The model was programmed with P-Spice, a software specifically designed for simulating electrical circuits but easily adaptable to physiology. Simulations of internal water fluxes, sucrose concentrations and fruit growth rates are given for different conditions of soil water availability and hydraulic resistances (sensitivity analysis). The discussion focuses on the potential interest of this approach in functional--structural plant models to address water stress-induced effects.     

Effects of Tapping, Wounding, and Growth Regulators on Turgor Pressure in Hevea brasiliensis Muell. Arg.

Various forms of wounding result in increases in hydrostaticpressure in the laticiferous phloem tissue of Hevea brasiliensis;regular tapping, a form of controlled wounding, probably causesa similar response. When a tree is ring-barked, there is a transientfall in turgor immediately above and below the ring, presumablyowing to loss of latex during cutting. This is followed by apressure increase which is particularly marked above the ring,suggesting the accumulation of metabolites. Isolation of an‘island’ of tissue, by cuts down to the wood, resultsin a steep fall in turgor within it, although a relatively slowrecovery may follow. Partially isolated panels show smallerfalls and a more rapid rise. It appears that a functional phloemconnexion permits a more rapid recovery of osmotic and turgorpressures following latex losses, both in the isolation experimentsand in normal tapping. Growth regulators such as 2,4,5-trichlorophenoxyaceticacid (2,4,5-T) increase latex yields by prolonging latex flowafter tapping. In untapped trees treatment with 2,4,5-T resultsin a slow and fairly small increase in turgor pressure, butthis effect may not be apparent if trees are regularly tapped.When the tapping cut is opened, there is a rapid fall in pressureimmediately under the cut. This loss in turgor spreads throughthe latex-vessel system as latex flows towards the cut, butrecovery is apparent near the cut even before flow ceases. Pressuregradients indicate a rapid formation of a localized resistanceto flow at or near the cut surface. This process appears toplay a major part in restricting flow. The increased yieldswhich result both from regular tapping and after 2,4,5-T treatmentappear to result from a delay in this sealing process. The mechanismsby which the barrier to flow is built up and delayed by 2,4,5-Ttreatment are not clearly understood.     

Differences in membrane selectivity drive phloem transport to the apoplast from which maize florets develop

Background and Aims

Floral development depends on photosynthetic products delivered by the phloem. Previous work suggested the path to the flower involved either the apoplast or the symplast. The objective of the present work was to determine the path and its mechanism of operation.

Methods

Maize (Zea mays) plants were grown until pollination. For simplicity, florets were harvested before fertilization to ensure that all tissues were of maternal origin. Because sucrose from phloem is hydrolysed to glucose on its way to the floret, the tissues were imaged and analysed for glucose using an enzyme-based assay. Also, carboxyfluorescein diacetate was fed to the stems and similarly imaged and analysed.

Key Results

The images of live sections revealed that phloem contents were released to the pedicel apoplast below the nucellus of the florets. Glucose or carboxyfluorescein were detected and could be washed out. For carboxyfluorescein, the plasma membranes of the phloem parenchyma appeared to control the release. After release, the nucellus absorbed apoplast glucose selectively, rejecting carboxyfluorescein.

Conclusions

Despite the absence of an embryo, the apoplast below the nucellus was a depot for phloem contents, and the strictly symplast path is rejected. Because glucose and carboxyfluorescein were released non-selectively, the path to the floret resembled the one later when an embryo is present. The non-selective release indicates that turgor at phloem termini cannot balance the full osmotic potential of the phloem contents and would create a downward pressure gradient driving bulk flow toward the sink. Such a gradient was previously measured by Fisher and Cash-Clark in wheat. At the same time, selective absorption from the apoplast by the nucellar membranes would support full turgor in this tissue, isolating the embryo sac from the maternal plant. The isolation should continue later when an embryo develops.     

Phloem Pressure Differences and C-Assimilate Translocation in Ecballium elaterium

The role of phloem turgor pressure in ¹⁴C-assimilate translocation in Ecballium elaterium A. Rich was studied. The direction of translocation was manipulated by two methods: darkening, or defoliation, of the upper or lower halves of the shoots. After 24 hours of labeled assimilate movement, sieve tube turgor levels were measured with the phloem needle technique. Distribution of label, determined by autoradiography and counting, revealed a direct correlation between the direction of assimilate transport and the pressure difference. Phloem turgor levels always decreased in the stem of darkened shoots; this resulted in greater pressure differences in the stem between the source leaf receiving ¹⁴CO₂ and treated regions.     

Characterization and correlation of DC electrical penetration graph waveforms with feeding behavior of beet leafhopper, Circulifer tenellus

Feeding behavior of beet leafhopper, Circulifer tenellus (Baker) (Homoptera: Cicadellidae), was studied with a DC electrical penetration graph. Nine different electrical penetration graph waveforms associated with feeding were identified and characterized. Waveforms were correlated with specific feeding behaviors using a number of techniques, including high magnification video recording, honeydew analysis, stylectomy, and histological processing. Waveforms were grouped into three phases based on feeding behavior: pathway phase (waveforms A, B1, B2, and C), non-phloem ingestion phase (waveform G), and phloem phase (waveforms D1, D2, D3, and D4). No ingestion was found to occur during waveforms A, B1, B2, and C. Waveform G was associated primarily with ingestion of xylem sap and occasionally with ingestion of mesophyll sap. Stylet tips were located in phloem during waveforms D1, D2, and D3, and waveforms D2 and D3 were correlated with ingestion of phloem sap. Waveform D4 probably also plays a role in phloem ingestion, because D4 is very brief and always occurs embedded in either waveform D2 or D3. In contrast to most other homopteran insects, rate of honeydew production (and hence rate of ingestion) was much lower on phloem than on xylem. More rapid rates of ingestion are expected on phloem, because its high turgor pressure drives sap into the feeding insect whereas the negative pressure of xylem sap is expected to cause a slow rate of ingestion. The very slow ingestion rate of beet leafhopper feeding on phloem suggests that it is not able to exploit the high turgor pressure of phloem to achieve the high rate of ingestion that is typical of phloem ingestion by other insects.