Effect of Abscisic Acid on Sorbitol Uptake in Growing Apple Fruits

Levels of abscisic acid (ABA) in the fruit flesh of developingapples (cv. Golden Delicious) were measured by electron capturegas chromatography. ABA content of the tissue, calculated ona fresh weight basis, decreased at a constant rate from 200µg g^–1 in young fruit to 10 µg g^–1 inolder fruit and then increased when the ripening process commenced.On a whole fruit basis, the ABA level increased during the initialphase of fruit growth, remained constant during the linear growthphase and increased again when fruits started to ripen. During fruit development the ABA content correlated with therate of sorbitol uptake, when measured after discs of fruittissue were incubated in [¹⁴C]sorbitol. Sorbitol uptake washigh during the initial growth phase and declined at a constantrate during fruit development. ABA present in the incubation medium stimulated sorbitol uptakeinto fruit tissue at concentrations higher than 10^–8 M,whereas indolyl-3-acetic acid had no effect on uptake. When comparing sorbitol uptake in different zones of young fruit,it was found that uptake was higher in discs of outer fruitlayers than in discs from inner fruit zones. Key words: Pyrus malus, Apple, Abscisic acid, Sorbitol     

The Effect of Low Osmotic Potential on Phosphate Uptake and Metabolism by Beetroot Discs

The uptake of phosphate by aged beetroot discs was examinedunder a range of water deficits which were induced osmoticallywith mannitol or polyethylene glycol At low water potentialsthe absorption of labelled phosphate was enhanced when the ambientconcentration of phosphate was high (10^–3 M) and the timefor absorption was short (30 mm): this occurred even when themetabolism was inhibited (by the water deficit), as indicatedby lowered oxygen consumption and incorporation of ³³P intohexose-phosphate, phosphoglycenc acid, a liquid fraction, anda precipitate consisting mainly of cell walls. The Q₁₀ of theuptake process approached unity at these low water potentials.Accompanying the enhanced uptake there was an increase in leakageof previously absorbed phosphate. It is postulated that thestimulation in uptake of phosphate in low osmotic potentialswas due to an increase in permeability Over long periods (6 h) uptake was inhibited by treatment atlow osmotic potentials. This is interpreted in terms of inhibitionof a metabolic component of phosphate uptake.     

Seed Water Relations and the Regulation of the Duration of Seed Growth in Soybean

Soybean [Glycine max (L.) Merrill] seeds and cotyledons weregrown in an in vitro culture system to investigate the relationshipsbetween cell expansion (net water uptake by the seed) and drymatter accumulation. Seeds or cotyledons grown in a completenutrient medium containing 200 mol m^–3 sucrose continueddry matter accumulation for up to 16 d after in planta seedsreached physiological maturity (maximum seed dry weight). Seedor cotyledon water content increased throughout the cultureperiod and the water concentration remained above 600 g kg^–1fresh weight. These data indicate that the cessation of seeddry matter accumulation is controlled by the physiological environmentof the seed and is not a pre-determined seed characteristic.Adding 600 mol m^–3 mannitol to the medium caused a decreasein seed water content and concentration. Seeds in this mediumstopped accumulating dry matter at a water concentration ofapproximately 550 g kg^–1. The data suggest that dry matteraccumulation by soybean seeds can continue only as long as thereis a net uptake of water to drive cell expansion. In the absenceof a net water uptake, continued dry matter accumulation causesdesiccation which triggers maturation. Key words: Glycine max (L.) Merrill, solution culture, duration of seed growth, water content, dry matter accumulation     

The Carbon Economy of Rubus chamaemorus L. II. Respiration

Respiratory activity and seasonal changes in carbohydrate contentof the storage organs of Rubus chamaemorus L. have been investigated.Leaf dark respiration rate increases in a non-linear mannerfrom 0·7 mg CO₂ evolved dm^–2 h^–1 at 0 °Cto 4·6 rng CO₂ evolved dm^–2 hh^–1 at 30 °C.Root and rhizome respiration rates increase from 1 µ1O₂ uptake g^–1 fresh weight h^–1 at 0.7 ° C to10 µ10, uptake g^–1 f. wt h^–1 at 20 °C.Rhizome carbohydrate reserves decline from a September peakof 33 per cent alcohol insoluble d. wt to 16 per cent in May. The circumpolar distribution of R. chamaemorus is discussedin relation to the evidence presented here and in the precedingpaper of the series.     

Methanol Accumulation in Maturing Seeds

During in vitro growth and maturation of soybean seeds, cessationof embryo growth and dry weight accumulation occurred in thepresence of abundant C and N nutrients. Axis followed by cotyledontissues changed from green to yellow, and post-harvest germinationpotential declined if cultured after yellowing of axis tissues.A tissue specific accumulat;on of methanol occurred during thein vitro culture of immature seeds (i.e. initially 50 to 70mg fresh weight) to maturity in liquid medium. Methanol accumulatedto 3.0 g m^–3 or 50 µg seed^–1 in the medium,while methanol decreased from 37 to about 3.0 µg g^–1fresh weight in cotyledons. By contrast, axis tissues increased20-fold in methanol concentration to 90 µg g^–1 during20 d in culture. Ethanol was present only in trace amounts inaxis tissues and medium. Addition of exogenous methanol vapourto in situ grown seeds during precocious maturation decreasedsubsequent seedling vigour and germination with increasing levelsof exposure. Methanol accumulation in axis tissues during thegermination phase was not correlated with high temperature andtissue water content treatments which simulated pre-harvestdeterioration of seeds. However, the accumulation of methanolduring in vitro seed development and maturation in liquid culturemay contribute to reduced post-harvest germination performance. Key words: Soybean, Glycine max, seed maturation, in vitro, methanol     

The Theory and Practice of Measuring Transport Coefficients and Sap Flow in the Xylem of Red Maple Stems (Acer rubrum)

In this paper we report measurements concerning the conductivityof water and ions and the interaction between the two in excisedpieces of xylem of red maple stems under various conditions.We have also demonstrated that it is possible to detect theflow of solutions through the stems of maple by measuring thedegree of interaction between the flow of water and ions. Inthis technique we apply voltage pulses of ±V volts acrossa length of stem and detect the unequal current pulses resultingfrom the greater frictional drag when current (which is carriedprimarily by cations) is flowing against the water stream thanwhen flowing with the water stream. The hydraulic conductivityof recent maple sapwood ranges from 30 to 90 cm³ s^–1 cm^–2(J cm^–3)^–1 cm; in 2 mM KCl the electrical conductivityis roughly 3 x 10^–4 mho cm^–1 and the electro-kineticcross coefficient is roughly 4x10^–5 A cm^–2 (J cm^–3)^–1cm.     

An Examination, by Compartmental Flux Analysis, of the Development of Sodium and Chloride Absorption Capacities in Beetroot Disks

Using beetroot, Beta vulgaris L. var. Avon Early, grown in radioactivelylabelled nutrient solutions, concentrations and fluxes of Na⁺and Cl^– were estimated for cells of freshly cut storageroot disks, by compartmental analysis of radioisotope elutionmeasurements. These values were compared with results obtainedin a similar manner from beetroot grown in non-labelled nutrientsolution and loaded instead during an aging period in ²²Na-or ³⁶Cl- labelled 1 mM NaCl solution. In accord with the generallyaccepted, but never properly tested, view, it was found thatnet Na⁺ influx followed from a reduction in efflux with agingand net Cl^– uptake depended on a marked increase in influx.However, both these important changes took place at the tonoplast,and, although aging led to a reduction of plasmalemma fluxes,at no time was entry of Cl^– into the cytoplasm, or lossof Na⁺ from the cytoplasm, significantly restricted.     

Ethylene and Ethane Production in 2,4-D Treated and Salt Treated Tobacco Tissue Cultures

Gas chromatography was used to measure ethylene (ethene) andethane production by tobacco (Nicotiana tabacum cv. Wisconsinno. 38) callus tissues grown on media containing inorganic saltsaccording to Murashige and Skoog (1962), sucrose, myo-inositol,thiamine-HCl kinetic according to Linsmaier and Skoog (1965),and either 2,4-dichiorophenoxyacetic acid (2,4-D) in the range0–100 mgl^–1 or 2 mgl^–1 indoi-3-ylacetic acidplus NaCl in the range 0–200 Meq l^–1. Ethylene productionrates were high (> 500 nl h^–1 g^1– fresh weight)initially in all treatments. Subsequently, ethylene productiondeclined in rapidly growing cultures but remained high in moderatelyand severely 2,4-D (> 0·5 mgl^–1) stressed andin severely NaCl (150 Meql^–1) stressed cultures. Highinitial rates of ethane production (> 200 nl h^–1 g^–1fresh weight) were obtained under conditions of severe stresscaused by 2,4-D or NaCl but not in control or moderately inhibitedcultures. With further incubation ethane production declinedin the severely stressed cultures. It is concluded that ethyleneproduction can be used as an index of moderate 2,4-D stressand severe NaCl stress by virtue of the high persisting ratesof ethylene production in stressed cultures. Ethane productioncan be used as an early index of severe stress caused by either2,4-D or NaCl in vitro. Nicotiana tabacum L., tobacco, ethylene, ethenen, ethane, 2,4-dichlorophenoxyacetic acid, auxin, stress, callus tissue     

Fermentation Rates and Ethanol Accumulation in Relation to Flooding Tolerance in Rhizomes of Monocotyledonous Species

Under anoxia an accumulation of ethanol took place in all species.Lactic fermentation was found to be of less importance in everycase. The amount of ethanol accumulated depended on the abilityof the rhizome to eliminate it from its tissues. Despite greatvariations in fermentative capacity as seen in the ADH measurementsthe wetland species did not accumulate ethanol to concentrationsgreater than 30 µmol g^–1 fresh weight. This representeda plateau above which the ethanol concentration did not riseeven with continued anaerobic incubation. No such plateau ofethanol accumulation was found in the dryland species Iris germanicawhich accumulated ethanol steadily reaching concentrations of70 µmol g^–1 fresh weight. If ethanol is toxic to higher plant tissues then the steadystate condition of low ethanol accumulation found in wetlandspecies will minimize this danger. Key words: Ethanol, Flooding, Rhizomes     

Development and Control of the Number of Flowers per Node in Pisum sativum L.

Non-dormant flower initials are laid down in the axils of successiveleaf initials as they are formed by the apical meristem of Pisumsativum L. In cultivars with a maximum capability of two flowersper raceme, the undeveloped flower meristem divides into twoportions. One forms the first flower and the other either developsinto a small protrusion on one side of the first flower or becomesthe second flower, depending on the prevailing environment.Flower development in conditions favouring single-flowered racemeswas advanced by one plastochron. Variation in the number offlowers per raceme occurs between cultivars and between environments.The number of double flowers formed was favoured by higher lightintensity (120 Js^–1 m^–2) and carbon dioxide concentration(330 µ11^–) and lower temperature (15°C). Incultivars producing more than two flowers per raceme, lowerlight intensity (60 Js^–1 m^–2) plus higher temperature(20°C) increased the mean number of flowers per raceme.Soluble sugar levels in all varieties were higher (36.05 mgeq glucose g^–1 fresh weight) in the low temperature/highlight environment than the high temperature/low light environment(14.80 mg eq glucose g^–1 fresh weight). The flowering potential and stability of 13 cultivars have beenassessed in controlled environment and in sowing date trialsin the field. A stable variety, which consistently producedtwo flowers per raceme, was identified in controlled environmentand its stability was maintained in field trials. A linear regressionof stability of flower number in the field on stability in controlledenvironment accounted for 89.6 per cent of the variance (P<5per cent), but the flowering potential in a sowing date experimentwas not related to temperature or radiation intensity.     

Melibiose, A Suitable, Non-Permeating Osmoticum for Suspension-Cultured Tobacco Cells

Dracup, M., Gibbs, J. and Greenway, H. 1986. Melibiose, a suitablenon-permeating osmoticum for suspension-cultured tobacco cells.—J.exp. Bot. 37: 1079–1089. A neutral, non-permeating osmoticum with low molecular weightwas required for studies involving responses to water deficitand salinity by suspension-cultured cells of tobacco. For thispurpose, raffinose, sorbitol, mannitol and melibiose were evaluated. Raffinose was hydrolysed by cells which were then able to useone of the products, namely fructose, for growth. Sorbitol andmannitol were not used for growth but were taken up by cells.After 96 h in media containing 50 mol m^–3 of sorbitolor mannitol as the carbon source, cells contained 85 mol m^–3sorbitol or 45 mol m^–3 mannitol. At least part of theuptake of sorbitol would have been active as sorbitol was transportedagainst a concentration gradient. Melibiose was one of the products of hydrolysis of raffinoseand proved to be an effective osmoticum. When supplied as thesole source of sugar for cells, melibiose was neither hydrolysednor taken up by cells. Furthermore, melibiose was not toxicsince adding 50 mol m^–3 to a culture medium containingglucose did not affect growth of cells. Key words: Sorbitol, mannitol, uptake     

Polyamine Content in Relation to Embryo Growth and Dedifferentiation in Barley (Hordeum vulgare L.)

Putrescine, spermidine, and spermine content were analysed inzygotic embryos of barley (Hordeum vulgare L.). Changes in polyaminecontent were observed during zygotic embryo growth. In two cultivars,‘Bomi’ and ‘Golden Promise’, the totalpolyamine content in the embryos was 2.6–2.9 nmol mg^–1fresh weight 10 d after anthesis, the highest content observed.It dropped to 1.3 nmol mg^–1 fresh weight 14 d after anthesis.This drop was caused by decreases in all three polyamine concentrations.From 14 to 35 d after anthesis the putrescine content continuedto decrease while the spermidine and spermine content increased,thus the total polyamine content remained constant until 35d after anthesis. The mutant ‘Ris? 1508’ showeda constant polyamine content around 1.3 nmol mg^–1 freshweight from 14 to 35 d after anthesis. The polyamine patternwas conserved in all three lines throughout the period of investigationshowing a spermidine content higher than putrescine contentwhich was, in turn, higher or equal to the spermine content.The polyamine content measured as nmol µg^–1 proteindecreased from 14 to 21 d post anthesis in all three lines,because the protein content (µg mg^–1 fresh weight)increased during the period. In dedifferentiating zygotic embryoscultured in vitro the putrescine content (nmol mg^–1 freshweight) rose by a factor of nine and the spermidine contentdoubled within the first week of cultivation, whereas sperminecontent did not change. For embryoderived calli a repeated patternof change in polyamine content was observed throughout the subculturingperiod. Key words: Polyamines, Hordeum vulgare L., embryo development     

Turgor, Growth and Rheological Gradients of Wheat Roots Following Osmotic Stress

The growth rate of hydroponically grown wheat roots was reducedby mannitol solutions of various osmotic pressures. For example,following 24 h exposure to 0·96 MPa mannitol root elongationwas reduced from 1· mm h^–1 to 0·1 mm h^–1 Mature cell length was reduced from 290 µm in unstressedroots to 100 µm in 0·96 MPa mannitol. This indicatesa reduction in cell production rate from about 4 per h in theunstressed roots to 1 per h in the highest stress treatment. The growing zone extended over the apical 4·5 mm in unstressedroots but became shorter as growth ceased in the proximal regionsat higher levels of osmotic stress. The turgor pressure along the apical 5·0 mm of unstressedroots was between 0·5 and 0·6 MPa but declinedto 0·41 MPa over the next 50 mm. Following 24 h in 0·48(200 mol m^–3) or 0·72 MPa (300 mol m^–) mannitol,turgor along the apical 50 mm was indistinguishable from thatof unstressed roots but turgor declined more steeply in theregion 5·10 mm from the tip. At the highest level ofstress (0·96 MPa or 400 mol m^–3 mannitol) turgordeclined steeply within the apical 20 mm. Key words: Growth, turgor pressure, wall rheology, osmotic stress, osmotic adjustment     

CHANGES IN ACTIVITIES OF 5-DEHYDKOQUINATE HYDRO-LYASE AND SHIKIMATE-NADP OXIDOREDUCTASE IN SLICED SWEET POTATO ROOTS

Sweet potato roots of variety Norin No. 1 were cut into discs(319 mm), which were incubated at 28–29 for 4 days.At 24-hour intervals, activities of 5-dehydroquinate hydro-lyaseand shikimate-NADP oxidoreductase in the buffer extracts ofdiscs were estimated. The activities of both enzymes were significantlydetected in the fresh root tissues. 5-Dehydroquinate hydro-lyaseactivity per fresh weight increased by three to four times within2 days after slicing, and decreased gradually. Shikimate-NADPoxidoreductase activity at the lst-day incubation period wasfound to be about three times as much as the activity foundin the fresh roots, and it remained for 4 days after slicing.The role of these enzymes in polyphenol biosynthesis in thesliced root tissues is discussed. An attempt to detect the enzymicconversion of dehydroquinic acid to quinic acid is also described. ¹This paper constitutes Part 55 of the Phytopathological Chemistryof Sweet Potato with Black Rot. ²Present address: Department of Biology, Tokyo MetropolitanUniversity, Tokyo. Nagoya     

The Osmotic Pressure of Concentrated Solutions of Polyethylene Glycol 6000, and its Variation with Temperature

The vapour pressures of aqueous solutions of polyethylene glycol6000 have been measured (by equilibration with sucrose solutions)up to the saturation point at 25 °C (1.45 g g^–1 water).The reduced-osmotic-pressure (/c), when plotted versus concentration(c), rapidly and linearly increased up to a concentration ofabout 0.8 g g^–1 (crossing the similar plot for sucrose).Above this concentration, the reduced-osmotic-pressure rosemore slowly, but still more rapidly than sucrose. The maximumosmotic pressure achieved at saturation was nearly 18 MPa. Usingthe virial equation: /c= RT/M + RTA₂c, the calculated secondvirial coefficient (A₂) for the linear part is 4.5 x 10^–3mol g^–1, a value slightly greater than most literaturevalues at 25 °C. Data are cited showing that A₂ varies linearlyfrom 5–6 x 10^x3 at 0 °C, to zero at 80–90 °C     

Hormonal responses to partial drying of the root system of Helianthus annuus

Plants of Helianthus annuus were pot-grown in soil, with approximately30% of the root system protruding through the base. After 7d, the upper part of the root system of half of the plants wasexposed to drought (internal roots) while the lower part waskept in aerated nutrient solution (protruding root). The treatmentrapidly reduced the internal roots' water content from 26.1to 21.9 g g^–1 dry weight (DW), while in protruding rootsof stressed plants it slowly and continuously decreased from31.9 to 25.2 g g^–1 DW. Leaf water content rapidly decreasedin treated plants from 7.4 to 6.4 g g^–1 DW in the first2d and then reached a plateau. In stressed plants leaf stomatalresistance was significantly higher in the first 3 d while leafwater potential was lower only on the last day. Abscisic acid (ABA) concentration in treated plants increasedsignificantly compared to the controls. In treated internalroots, ABA rose from the first day, reaching a maximum of 1.48±0.49nmol g^–1 DW after 3 d. In treated protruding roots a maximumof 0.99±0.09 nmol g^–1 DW was reached after 1 d.ABA concentration in the xylem sap increased 2 d and 3 d afterthe start of soil drying, with a maximum of 113±12nmoll^–1 during the third day. The ABA rise in the leaves oftreated plants was less significant. Indol-3yl-acetic acid (IAA) concentration in internal rootsof treated plants reached a maximum of 22.54±3.34 nmolg^–1 DW on the third day, then decreased dramatically.The protruding root system of control plants showed a maximumvalue of 16.05±1.77 nmol g^–1 DW on the sixth day. Little difference in cytokinin content of xylem sap was notedbetween control and treated plants. Hormonal variations in different parts of the plant are discussedin relation to drought stress. Key words: Soil drying, roots, ABA, IAA, cytokinins     

Measurement of Yield Threshold and Cell Wal Extensibility of Intact Wheat Roots under Different Ionic, Osmotic and Temperature Treatments

Yield stress threshold (Y) and volumetric extensibility () arethe rheological properties that appear to control root growth.In this study they were measured in wheat roots by means ofparallel measurement of the growth rate (r) of intact wheatroots and of the turgor pressures (P) of individual cells withinthe expansion zone. Growth and turgor pressure were manipulatedby immersion in graded osmoticum (mannitol) solutions. Turgorwas measured with a pressure probe and growth rate by visualobservation. The influence of various growth conditions on Yand was investigated; (a) At 27 °C.In 0.5 mol m^–3 CaCl₂ r, P, Y and were20.7±4.6 µm min^–1, 0.77±0.05 MPa,0.07±0.03 MPa and 26±1.9 µm min^–1MPa^–1 (expressed as increase in length), respectively.Following 24 h growth in 10 mol m^–3 KC1 these parametersbecame 12.3±3.5 µm min^–1, 0.72±0.04MPa, 0.13±0.01 MPa and 21±0.7 µm min^–1MPa^–1. After 24 h osmotic adjustment in 150 mol m^–3mannitol/0.5 mol m^–3 CaCl₂ r= 19.6±4.2 µmmin^–1, P = 0.68±0.05 MPa and Y and were 0.07±0.04MPa and 30±0.2 µm min^–1 MPa^–01, respectively.After 24 h growth in 350 mol m^–3 mannitol/0.5 mol m^–3CaCl₂ r= 13.3±4.1 µm min^–1, P= 0.58±0.07MPa, Y=0.12±0.01 MPa and ø 32±0.2 tim min^–1MPa^–1. During osmotic adjustment in 200 mol m^–3mannitol/0.5 mol m^–3 CaCl₂, with or without KCl, the recoveryof growth rate corresponded to turgor pressure recovery (t1/2approximately 3 h). (b) At 15 °C. Lowered temperature dramatically influencedthe growth parameters which became r= 8.3±2.8 um min^–1,P=0.78 MPa, r=<0.2 MPa and =15±0.1 µm min^–1MPa^–1. Therefore, Y and are influenced by 10 mol m^–3 K⁺ ionsand low temperature. In each case the effective pressure forgrowth (P-Y) was large indicating that small fluctuations ofsoil water potential will not stop root elongation. Key words: Yield threshold, cell wall extensibility, wheat root growth, temperature, turgor pressur     

A Critical Assessment of the Role of Potassium and Osmolarity in Stomatal Opening

An attempt has been made to separate the osmotic effect fromthe ionic effect of KCI in stomatal responses. For this purposeisolated illuminated epidermis from species with and withoutsubsidiary cells were treated with KCI (0-250 mOs kg^–1)and with mannitol (0-250 mOs kg^–1). Since osmolarity wasmade the basis of comparison, the effect of mannitol had tobe observed immediately, before guard cell contents could haveleached into the incubation medium. When plotting aperturesagainst osmolarity sigmoid curves were obtained with KCI, butwith mannitol straight lines resulted provided that prior tostripping and incubation leaves were briefly illuminated. Whilst in lower concentrations (60 mOs kg^–1 for Viciafaba; 90 mOs kg^–1 for Zantedeschia aethiopica; 190 mOskg^–1 for Commelina communis) pores were wider in mannitolthan in KCI, in concentrations above these values the situationwas reversed. It appeared therefore that KCI had either an inhibitoryor a promoting effect. Inhibition was most pronounced when atthe beginning of incubation stomata were closed; the inhibitoryeffect on stomata without subsidiary cells occurred at low concentrations(0-60 mOs kg^–1) whereas when subsidiary cells were presentinhibition occurred at up to 190mOs kg^–1. Other experiments started with KCI solutions of 50 mOs kg^–1for Vicia faba, 85 mOs kg^–1 for Zantedeschia aethiopicaand 115 mOs kg^–1 for Commelina communism; mannitol wasadditionally used to give the progressive increases in osmolarity.Degrees of opening were then reached which with KCI alone couldonly be attained at the very highest concentrations. Starch disappearance was followed using the periodic-acid-silvertest; by using either ⁸⁶Rb or ⁴³K it was shown that ion uptakewas restricted to guard cells alone only at osmolarities exceeding200 mOs kg^–1. On the basis of these observations it was concluded that K transportdoes not represent the major mechanism of stomatal regulation. Key words: Stomata, Potassium, Osmolarity     

A simple method for the isolation of intact mesophyll protoplasts from cereal plants

Intact mesophyll protoplasts from cereal plants were easilyprepared by incubating leaves with the abaxial epidermis peeledoff at 20–25?C for 2–3 hr in 0.6 M mannitol containing1% cellulase at pH 5.6. From one gram (fresh weight) of leaves1.5–6?10⁶ protoplasts, more than 90% of which were morphologicallyintact, could be obtained. Protoplasts isolated from wheat,oat, corn and barley were efficiently infected with brome mosaicvirus (BMV), and supported viral multiplication. (Received June 21, 1977; )     

The Role of Transmembrane Electrical Potential in Determining the Absorption Isotherm for Chloride in Potato

Measurements have been made of the electrical potential differencebetween the vacuoles of single potato tuber cells and externalCl^- solutions over the range 1–40 mM. With K⁺ as the counter-ion,the relationship between this transmembrane electrical potentialand external Cl^- concentration, for fresh cells at 20° C,was found to be one of decreasing negative polarity with increasingCl^- concentration (E at 1 mM Cl^- external = – 81 m V;change in E for a 10-fold change in external concentration,E₁₀ = 46 m V). The linearity of this relationship, apparenton a semi-logarithmic plot, was virtually unaltered by low temperature(0.5–2.5° C) or by previous ageing of the cells forperiods up to four days (indicating that metabolic ion absorptionis not an electrogenic process). When the counter-ion was maintainedat a constant high concentration (40 mM K⁺), the change in potentialover the Cl^- concentration range was only 4 m V, polarity becomingmore negative with increasing Cl^- concentration. With Ca⁺⁺ asthe counter-ion, the potential to external Cl^- concentrationrelationship was similar to that found in KCl solutions, exceptthat E₁₀ was only about 20 m V. Curves for the influx of C1^- to be expected on the basis ofthese electrochemical data alone have been shown to run closelyparallel to Cl^– absorption isotherms previously determinedexperimentally. This confirms the opinion, already formed onthe basis of theoretically derived values for passive Cl^- influx,that Cl^- uptake by both fresh and one-day-aged potato tissue,from KCl solutions and Cl^- solutions with a fixed high K⁺ concentration,is rate-determined at o° C by passive movement across theplasmalemma. Uptake of Cl^- by fresh tissue at 20° C appearsto be similarly regulated. No such parallelism was found between observed and expectedpatterns of Cl^- uptake from CaCl₂ solutions, or from KCl bytwo-day-aged tissue, and here factors in addition to the electrochemicalones must determine low temperature Cl^-uptake.