The Effect of Inorganic Nutrients on the Hormonal Requirements of Normal, Habituated, and Crown-gall Tissue 4

The addition of Braun and Wood's inorganic supplements (845mg l^–1 KCl, 1800 mgl^–1 NaNO₃, 300 mg l^–1 NaH₂PO₄.2H₂O,790 mg l^–1 (NH₄)₂SO₄) to White's medium caused markedincreases in the growth of normal tissues of Helianthus annuus,Nicotiana rustica, Daucus carota, and Vinca rosea and crown-galltumour tissues of H. annuus. However, no evidence was obtainedwhich suggested that the presence of these extra salts markedlyinfluenced the essential requirements of normal callus for auxinsand kinetin. In contrast their presence significantly influencedthe hormonal requirements of certain habituated cultures ofH. annuus and V. rosea. These habituated cultures had specificauxin requirements on White's medium while either an auxin orkinetin was sufficient on high-salts medium. These results arediscussed in relation to previous reports which suggested thatthe biosyntheses of auxins and other growth factors in normaland crown-gall cultures are specifically activated by certaininorganic ions.     

Modification of Stomatal Conductance by Sulphur Dioxide

The mechanism of SO₂-induced changes in stomatal conductance(g) of alder was examined to determine if SO₂ affects guardcell function directly or indirectly through the SO₂-inducedchanges in photosynthesis. During experimental fumigations at SO₂ concentrations of 3–3µmol m^–3 (0.08 µl l^–1), stomatal closurepreceded declines in net photosynthetic rate (A), indicatingthat SO₂ can directly affect guard cells. From these and otherstudies it appears that the sequence of A and g responses maybe influenced by SO₂ concentration as well as by species. Fumigation with SO₂ did not cause increases in g, even whenthe intercellular substomatal CO₂ concentration (c_i) was reducedby 50 µmol mol^–1. Increases in g are not attributableto SO₂ effects on the CO₂-based stomatal control system. Key words: Air pollution, Alnus serrulata, gas exchange, stomata, sulphur dioxide     

The Sensitivity of Net Photosynthesis in Several Plant Species to Short-term Fumigation with Sulphur Dioxide

The effects of exposure of up to 2 h with sulphur dioxide ona range of plant species was observed by measuring changes inthe rate of net photosynthesis under closely controlled environmentalconditions. Ryegrass, Lolium perenne ‘S23’ was thespecies most sensitive to SO₂; significant inhibition was detectedat 200 nl l^–1. Fumigations at 300 nl l^–1 also inhibitedphotosynthesis in field bean (Vicia faba cv. ‘Three FoldWhite’ and ‘Blaze’) and in barley (Hordeumvulgare cv. ‘Sonja’). No effect was detected inwheat (Triticum aestivum cv. ‘Virtue’) at concentrationsup to 600 nl l^–1 SO₂, or in oil-seed rape (Brassica napuscv. ‘Rafal’) except at 800 nl l^–1 SO₂). Recoverycommenced immediately after the fumigation was terminated andwas complete within 2 h when inhibition had not exceeded 20%during the SO₂ treatment. Key words: Sulphur dioxide, short-term fumigation, photosynthesis     

The Conductance of the Plasmalemma for CO2

Permeability coefficients (P_S values) for CO₂ of the plasmamembrane (PM) of the unicellular green algae Eremosphaera viridis,Dunaliella parva, and Dunaliella acidophila, and of mesophyllprotoplasts isolated from Valerianella locusta were determinedfrom ¹⁴CO₂ uptake experiments using the rapid separation ofcells by the silicone oil layer centrifugation technique. Theexperimental P_S values were compared with calculated numbersobtained by interpolation of Collander plots, which are basedon lipid solubility and molecular size, for D. parva cells,mesophyll protoplasts isolated from Spinacia oleracea, mesophyllcells and guard cells of Valerianella, and guard cell protoplastsisolated from Vicia faba. The conductivity of algal plasma membranes for CO₂ varies between0.1 and 9 ? 10^–6 m s^–1, whereas for the plasmalemmaof cells and protoplasts isolated from leaves of higher plantsvalues between 0.3 and 11 ? 10^–6 m s^–1 were measured.By assuming that these measurements are representative for plantsand algae in general, it is concluded that the CO₂ conductivityof algal PM is of the same order of magnitude as that of thehigher plant cell PM. P_s values of plasma membranes for CO₂are lower than those for SO₂, but are in the same order of magnitudeas those measured for H₂O. On the basis of these results itis concluded that theoretical values of about 3000 ? 10^–6m s^–1 believed to be representative for higher plant cells(Nobel, 1983) and which are frequently used for computer-basedmodels of photosynthesis, lack experimental confirmation andrepresent considerable overestimations. However, with severalsystems, including higher plant cells, the conductance of thePM for CO₂ was significantly higher in light than in darkness.This suggests that in light, additional mechanisms for CO₂ uptakesuch as facilitated diffusion or active uptake may operate inparallel with diffusional uptake. Key words: Conductivity, CO₂, permeability coefficient, photosynthesis, plasmalemma     

Changes in Growth and Quality Characteristics of Lucerne (Medicago sativa L.) in Response to Sulphur Dioxide Exposure under Field Conditions

The effects of SO₂ on some growth and quality characteristicsof lucerne (Medicago sativa L.) were investigated by exposingplants to mean SO₂ concentrations of 215, 78 or 2.8 µgm_–3 in open-top chambers for 166 d. Plants exposed to215 µg m_–3 had significantly lower shoot and rootweights compared with plants exposed to 78 µg m^–3,but not compared with control plants. Exposure to 215 or 78µg m ^–3 increased the plant shoot: root ratio, buthad no effect on leaf area. During the middle of the fumigationperiod, relative growth rate and net assimilation rate werehighest in plants exposed to 215 fig m, but these later fellbelow control values, and plants exposed to 78 µg m^–3had the highest relative growth rate and net assimilation rate.As the duration of exposure increased, an initial SO₂-inducedstimulation of growth may have developed to toxicity at thehighest SO₂ exposure. Exposure to SO₂ depressed L-ascorbic acid concentrations inleaves, had no effect on foliar protein or starch concentrations,and increased the specific energy of shoots and plant sulphurconcentrations. The effect of SO₂ on L-ascorbic acid concentrationsmay suggest a mechanism for reduced freezing tolerance of plantsafter exposure to SO₂. Key words: SO₂, Medicago sativa L., Growth     

Effect of irradiance and vapour pressure deficit On stomatal response to CO2 enrichment of four tree species

The stomatal response of seedlings grown in 360 or 720 µmolmol^–1 to irradiance and leaf-to-air vapour pressure deficit(VPD) at both 360 and 720 µmol mol^–1 to CO₂ wasmeasured to determine how environmental factors interact withCO₂ enrichment to affect stomatal conductance. Seedlings offour species with different conductances and life histories,Cercis canadensis (L.), Quercus rubra (L.), Populus deltoides(Bartr. ex Marsh.) P. nigra (L.), and Pinus taeda (L.), weremeasured in hopes of identifying general responses. Conductanceof seedlings grown at 360 and 720 µmol mol^–1 CO₂were similar and responded in the same manner to measurementCO₂ concentration, irradiance and VPD. Conductance was lowerfor all species when measured at 720 than when measured at 360µmol mol^–1 CO₂ at both VPDs ({small tilde}1.5 and{small tilde}2.5 kPa) and all measured irradiances greater thanzero (100, 300, 600,>1600 µmol m^–2 S^–2)The average decrease in conductance due to measurement in elevatedCO₂ concentration was 32% for Cercis, 29% for Quercus, 26% forPopulus, and 11% for Pinus. For alt species, the absolute decreasein conductance due to measurement in CO₂ enrichment decreasedas irradiance decreased or VPD increased. The proportional decreasedue to measurement in CO₂ enrichment decreased in three of eightcases: from 0.46 to 0.10 in Populus and from 0.18 to 0.07 inPinus as irradiance decreased from>1600 to 100 µmolm^–2 s^–1 and from 0.35 to 0.24 in Cercis as VPD increasedfrom 1.3 to 2.6 kPa. Key words: Stomatal conductance, CO₂ enrichment, irradiance, vapour pressure deficit     

Biochemical Limitations to Carbon Assimilation in C3 Plants--A Retrospective Analysis of the A/Ci Curves from 109 Species

Species-specific differences in the assimilation of atmosphericCO₂ depends upon differences in the capacities for the biochemicalreactions that regulate the gas-exchange process. Quantifyingthese differences for more than a few species, however, hasproven difficult. Therefore, to understand better how speciesdiffer in their capacity for CO₂ assimilation, a widely usedmodel, capable of partitioning limitations to the activity ofribulose-1,5-bisphosphate carboxylase-oxygenase, to the rateof ribulose 1,5-bisphosphate regeneration via electron transport,and to the rate of triose phosphate utilization was used toanalyse 164 previously published A/C_i, curves for 109 C₃ plantspecies. Based on this analysis, the maximum rate of carboxylation,Vc_max, ranged from 6µmol m^–2 s^–1 for the coniferousspecies Picea abies to 194µmol m^–2 s^–1 forthe agricultural species Beta vulgaris, and averaged 64µmolm^–2 s^–1 across all species. The maximum rate ofelectron transport, J_max, ranged from 17µmol m^–2s^–1 again for Picea abies to 372µmol m^–2 s^–1for the desert annual Malvastrum rotundifolium, and averaged134µmol m^–2 s^–1 across all species. A strongpositive correlation between Vc_max and J_max indicated that theassimilation of CO₂ was regulated in a co-ordinated manner bythese two component processes. Of the A/C_i curves analysed,23 showed either an insensitivity or reversed-sensitivity toincreasing CO₂ concentration, indicating that CO₂ assimilationwas limited by the utilization of triose phosphates. The rateof triose phosphate utilization ranged from 4·9 µmolm^–2 s^–1 for the tropical perennial Tabebuia roseato 20·1 µmol m^–2 s^–1 for the weedyannual Xanthium strumarium, and averaged 10·1 µmolm^–2 s^–1 across all species. Despite what at first glance would appear to be a wide rangeof estimates for the biochemical capacities that regulate CO₂assimilation, separating these species-specific results intothose of broad plant categories revealed that Vc_max and J_maxwere in general higher for herbaceous annuals than they werefor woody perennials. For annuals, Vc_max and J_max averaged 75and 154 µmol m^–2 s^–1, while for perennialsthese same two parameters averaged only 44 and 97 µmolm^–2 s^–1, respectively. Although these differencesbetween groups may be coincidental, such an observation pointsto differences between annuals and perennials in either theavailability or allocation of resources to the gas-exchangeprocess. Key words: A/C_i curve, CO₂ assimilation, internal CO₂ partial pressure, photosynthesis     

Regulation of the epithelial Na+ channel by intracellular Na+

The hypothesis that the intracellularNa⁺ concentration([Na⁺]_i)is a regulator of the epithelialNa⁺ channel (ENaC) was tested withthe Xenopus oocyte expression systemby utilizing a dual-electrode voltage clamp.[Na⁺]_iaveraged 48.1 ± 2.2 meq (n = 27)and was estimated from the amiloride-sensitive reversal potential.[Na⁺]_iwas increased by direct injection of 27.6 nl of 0.25 or 0.5 MNa₂SO₄.Within minutes of injection,[Na⁺]_istabilized and remained elevated at 97.8 ± 6.5 meq(n = 9) and 64.9 ± 4.4 (n = 5) meq 30 min after theinitial injection of 0.5 and 0.25 MNa₂SO₄,respectively. This increase of[Na⁺]_icaused a biphasic inhibition of ENaC currents. In oocytes injected with0.5 MNa₂SO₄(n = 9), a rapid decrease of inwardamiloride-sensitive slope conductance(g_Na) to 0.681 ± 0.030 of control within the first 3 min and a secondary, slowerdecrease to 0.304 ± 0.043 of control at 30 min were observed.Similar but smaller inhibitions were also observed with the injectionof 0.25 MNa₂SO₄.Injection of isotonicK₂SO₄(70 mM) or isotonicK₂SO₄made hypertonic with sucrose (70 mMK₂SO₄-1.2M sucrose) was without effect. Injection of a 0.5 M concentration ofeitherK₂SO₄,N-methyl-D-glucamine (NMDG) sulfate, or 0.75 M NMDG gluconate resulted in a much smaller initial inhibition (<14%) and little or no secondary decrease. Thusincreases of[Na⁺]_ihave multiple specific inhibitory effects on ENaC that can betemporally separated into a rapid phase that was complete within 2-3 min and a delayed slow phase that was observed between 5 and 30 min.

     

Influence of SO2 and NO2 Exposure on Glutathione, Superoxide Dismutase and Glutathione Reductase Activities in Scots Pine Needles

A 50-year-old Pinus sylvestris L. stand was exposed for 2 yearsto low concentrations of SO₂ and NO₂ in an open-air exposureexperiment in northern Sweden. The mean SO₂ concentrations inthe centre of the exposed plot during the 1988 exposure from14 June to 25 September, and during the 1989 exposure from 6June to 30 September were 15 nl 1^–1 and 12 nl 1^–1,respectively. The corresponding values for NO₂ were 15 nl 1^–1and 10 nl 1^–1, respectively. The concentration in thecontrol plot was never higher than a few ppb, and mostly below1 nl 1^–1. Needles sampled from the SO₂ and NO₂-exposed area showed reducedactivities of glutathione reductase (GR; EC 1.6.4.2 [EC] ) and superoxidedismutase (SOD; EC 1.15.1.1 [EC] ) compared with controls. The GRactivity showed decreased levels in autumn and winter, whilethe exposure had ceased, and SOD showed decreased activity duringthe second summer of exposure. Neither membrane-bound nor water-solubleanti-oxidants such as -tocopherol, carotenoids or glutathionechanged due to the exposure. The sulphur/nitrogen ratio wasincreased in needles that were exposed to SO₂ and NO₂ implyinga changed nutrition balance. The results suggest that the capacityof SOD and GR in the ascorbate-glutathione pathway was reduceddue to the exposure to air pollutants. Key words: Anti-oxidants, -tocopherol, glutathione, pigments, Pinus sylvestris L     

A sulfite-dependent adenosine triphosphatase of Thiobacillus thiooxidans. Its partial purification and some properties

A sulfite-dependent ATPase [EC 3.6.1.3 [EC] ] of Thiobacillus thiooxidanswas activated and solubilized by treatment with trypsin [EC3.4.4.4 [EC] ], and purified 84-fold with a 32% recovery. It requiredboth Mg²⁺ and SO₃^2– for full activity, and its optimumpH was found at 7.5–8.0. Mn²⁺, Co²⁺, and Ca²⁺ could partiallysubstitute for Mg²⁺, while SeO₃^2– and CrO₄^2– couldpartially substitute for SO₃^2–. The enzyme hydrolyzed ATP and deoxy-ATP most rapidly and otherphosphate esters were poorer substrates. The apparent Km valuefor ATP was 0.33 mM. The enzyme activity was strongly inhibitedby 0.2 mM NaN₃ and 10 mM NaF. (Received July 27, 1977; )     

A Comparative Study on the Effects of H2S and SO2 Fumigation on the Growth and Accumulation of Sulphate and Sulphydryl Compounds in Trifolium pratense L., Glycine max Merr. and Phaseolus vulgaris L.

Maas, F. M., De Kok, L. J., Peters, J. L. and Kuiper, P. J.C. 1987. A comparative study on the effects of H₂S and SO₂ fumigationon the growth and accumulation of sulphate and sulphydryl compoundsin Trifolium pratense L., Glycine max Merr. and Phaseolus vulgarisL.—J. exp. Bot. 38: 1459-1469. The effects of 0—25 mm³ dm³ H₂S and SO₂ on growth andsulphur content of shoots of Trifolium pratense, Glycine maxand Phaseolus vulgaris were studied. After 2 weeks of fumigationthe yield of T. pralense was reduced by 32% by H₂S, but notaffected by SO₂. Yield of G. max was not affected by H₂S, butreduced by 20% by SO₂, whereas that of P. vulgaris was increasedby 11% by H₂S and not affected by SO₂. Increases in sulphydrylcontent were already observed after 24 h of exposure to H₂Sand SO₂ in all plants. The increase was greatest in T. pratenseand smallest in P. vulgaris and, except for T. pratense, alwaysgreater in the H₂S-exposed than the SO₂-exposed plants. Oneday of exposure resulted in an increase in sulphate contentonly in the SO₂-fumigated plants, with the highest accumulationin T. pratense and the lowest in P. vulgaris. After 2 weeksan increase in sulphate content was also observed in the H₂S-exposedplants. This increase was also highest in T. pratense and lowestin P. vulgaris. Transpiration rate was not affected by a 24 h exposure to H₂Sor SO₂ and was highest in T. pratense, intermediate in G. maxand lowest in P. vulgaris. The order of theoretical rates of deposition of H₂S and SO₂correlated with the observed increases in sulphydryl contentduring the first 24 h of exposure in both H₂S and SO₂-fumigatedplants and with the increase in sulphate content in the SO₂-exposedplants. The increases in sulphydryl content were only 8% ofthe theoretical H₂S and SO₂-deposition fluxes, whereas sulphateaccumulation accounted for at least 57% of the theoretical SO₂-depositionflux. Key words: Air pollution, clover, French bean, Glutathione, Soybean, sulphur metabolism.     

Effects of Low Concentrations of Sulphur Dioxide on Net Photosynthesis and Dark Respiration of Vicia faba

Rates of net photosynthesis, P_N, and dark respiration of Viciafaba plants were measured in the laboratory in clean air andin air containing up to 175 parts 10^–9 (500 µg m^–3)SO₂. At all SO₂ concentrations exceeding 35 parts 10^–9,P_N was inhibited compared with clean air. At light saturation,the magnitude of inhibition depended on SO₂ concentration butat low irradiances the inhibition was independent of concentration.Dark respiration rates increased substantially, independentof concentration. When exposures continued for up to 3 days,P_N returned to clean air values about 1 h after fumigation ceased:dark respiration recovered after one photoperiod. There wereno visible injuries. Reviewing possible mechanisms responsible for the inhibitionof P_N, it is suggested that SO₂ competes with CO₂ for bindingsites in RuBP carboxylase. Analysis of resistance analoguesdemonstrates that SO₂ altered both stomatal and internal (residual)resistances. A model of crop photosynthesis shows the implications of theobserved responses for the growth of field crops in which plantsare assumed to respond like laboratory plants. Photosynthesisof the crop would be less sensitive than that of individualplants to SO₂ concentration. Daily dry matter accumulation ofhypothetical ‘polluted crops’ would be substantiallyless than clean air values but would vary relatively littlewith SO₂ concentration. It is concluded that physiological basesexist to account for observed reductions in growth of plantsat very low SO₂ concentrations, and that thresholds for plantresponses to SO₂ require reassessment.     

The Response of the C3-CAM Tree, Clusia rosea, to Light and Water Stress: I. GAS EXCHANGE CHARACTERISTICS

Gas exchange measurements were undertaken on 2-year-old plantsof Clusia rosea. The plants were shown to have the ability toswitch from C₃-photosynthesis to CAM and vice versa regardlessof leaf age and, under some conditions, CO₂ was taken up continuously,throughout the day and night. The light response was saturatedby 120 µmol m^–2 s^–1 typical of a shade plant. Gas exchange patterns in response to light, water and VPD wereexamined. All combinations of daytime and night-time CO₂ uptakewere observed, with rates of CO₂ uptake ranging from 2 to 11µmol m^–2 s^–1 depending upon water status andlight. Categorization of this plant asC₃, CAM or an intermediateis impossible. Differing VPD affected the magnitude of changesfrom CAM to C₃-photosynthesis (0 to 0.5 and 0 to 6.0 µmolm^–2 s^–1 CO₂, respectively) when plants were watered.Under well-watered conditions, but not under water stress, highPPFD elicited changes from CAM to C₃ gas exchange. This is unusualnot only for a shade plant but also for a plant with CAM. Itis of ecological importance for C. rosea, which may spend theearly years of its life as an epiphyte or in the forest understorey,to be able to maximize photosynthesis with minimal water loss. Key words: Clusia rosea, CAM, C₃, stress     

Crop load affects assimilation rate, stomatal conductance, stem water potential and water relations of field-grown Sauvignon blanc grapevines

The effects of two shoot densities (14 and 44 shoots/vine) andtwo crop levels (one and two clusters/shoot) on gas exchangeand water relations of field-grown Sauvignon blanc (Vitis viniferaL.) were studied in a factorial design over 3 years. The two-clustertreatments had 0.14 MPa higher stem water potential (_stem),1.4 µmol m^–2 s^–1 higher assimilation rate(A), 0.04 mol m^–2 s^–1 higher stomatal conductance(g_s) and 0.008 mol m^–2 s^–1 higher non-stomatal (g_m)conductance. The two-cluster treatments had higher g_s and transpirationrates than the one-cluster treatments, for similar _stem. A quantitativeanalysis suggests that storage capacity cannot account for thesimultaneous increase in g_s and _stem in the two-cluster treatments.Similar g_s-g_m responses were found In the one- and two-clustertreatments, regard less of differences between the treatmentsin g_s-_stem response. Key words: Grapevine, stomatal conductance, assimilation rate, water relations     

The Effects of Low Concentrations of Sulphur Dioxide on Stomatal Conductance and Epidermal Cell Survival in Field Bean (Vicia faba L.)

Exposure of 3 week old field bean plants to concentrations ofSO₂ from 50–500 µg m^-3 induced comparable 20–25%increases in mean leaf diffusive conductance regardless of whetherthe diffusive conductances were obtained by porometric measurementor calculation from gas exchange data. The stomatal conductancesof the adaxial and abaxial leaf surfaces were both increasedby exposure to SO₂. Microscopic examination of epidermal strips from control andpolluted plants revealed that the stomatal opening observedin treated plants was associated with a sharp reduction in theproportion of living epidermal cells adjacent to the stomata.The proportion of surviving adjacent epidermal cells was invariablysmaller on the lower epidermis and appeared to decrease as theSO₂ concentration was raised from 50 to 500 µg m^–3.Although the guard cells appeared to be undamaged at concentrationsbelow 200 µg m^–3, structural disorganization ordeath of one or both guard cells was observed frequently ator above 500 µg m^–3. The results are discussed in relation to the controversy concerningthe effects of SO₂ on stomatal aperture.     

Influence of Wind Speed on the Sensitivity of Ryegrass to SO2

The sensitivity of S23 Lolium perenne L. to 11 parts 10^–8SO₂ was investigated at two different wind speeds. At the higherwind speed of 25 m min^–8, SO₂ caused significant reductionsin leaf area, root/shoot ratio, and all dry weight fractionsmeasured. At the lower wind speed of 10 m min^–1 growthreductions were not found. The differences in sensitivity ofplants to SO₂ at different wind speeds is discussed in relationto boundary layer resistances of leaves. It is concluded thatthe sensitivity of a plant to a particular pollutant shouldno longer be measured in terms of only the concentration andlength of exposure.     

Occurrence of Inducible Crassulacean Acid Metabolism in Leaves of Talimum triangulare (Portulacaceae)

In this paper we report for the first time the occurrence ofan inducible weak CAM in leaves of Talinwn triangulare (Jacq.)Willd. This plant is a terrestrial perennial deciduous herbwith woody stems and succulent leaves which grows under fullexposure and in the shade in northern Venezuela. Plants grownin a greenhouse (‘sun’ plants) and a growth cabinet(‘shade’ plants) with daily irrigation showed CO₂uptake only during the daytime (maximum rate, 4?0 µmolm^–2 s^–1) and a small acid accumulation during thenight (6?0 µmol H⁺g^–1 FW). Twenty-four hours aftercessation of irrigation, no CO₂ exchange was observed duringpart of the night. Dark fixation reached a maximum (1?0 µmolCO₂ m^–2 s^–1, 100 µmol H⁺ g^–1 FW) onday 9 of drought. By day 30 almost no gas exchange was observed,while acid accumulation was still 10 µmol H⁺ g^–1FW. Rewatering reverted the pattern of CO₂ exchange to thatof a C₃ plant within 24 h. Daytime and night-time phosphoenolpyruvatecarboxylase activity increased up to 100% (shade) and 62% (sun)of control values after 10 and 15 d of drought, respectively.Light compensation point and saturating irradiance were similarin well-watered sun and shade plants, values being characteristicof sun plants. CAM seems to be important for the tolerance ofplants of this species to moderately prolonged (up to 2 months)periods of drought in conditions of full exposure as well asshade, and also for regaining high photosynthetic rates shortlyafter irrigation. Key words: Talinum triwigulare, inducible CAM, PEP-C activity, recycling     

C3 and CAM Photosynthetic Characteristics of the Submerged Aquatic Macrophyte Littorella uniflora: Regulation of Leaf Internal CO2 Supply in Response to Variation in Rooting Substrate Inorganic Carbon Concentration

The relationships between CO₂ concentrating mechanisms, photosyntheticefficiency and inorganic carbon supply have been investigatedfor the aquatic macrophyte Littorella uniflora. Plants wereobtained from Esthwaite Water or a local reservoir, with thelatter plants transplanted into a range of sediment types toalter CO₂ supply around the roots. Free CO₂ in sediment-interstitial-waterranged from 1–01 mol m^–3 (Esthwaite), 0.79 mol m^–3(peat), 0.32 mol m^–3 (silt) and 0–17 mol m^–3(sand), with plants maintained under PAR of 40 µmol m^–2s^–1. A comparison of gross morphology of plants maintained underthese conditions showed that the peat-grown plants with highsediment CO₂ had larger leaf fresh weight (0–69 g) andtotal surface area (223 cm² g^–1 fr. wt. including lacunalsurface area) than the sand-grown plants (0.21 g and 196 cm²g^–1 fr. wt. respectively). Root fresh weights were similarfor all treatments. In contrast, leaf internal CO₂ concentration[CO₂], was highest in the sand-grown plants (2–69 molm^–3, corresponding to 6.5% CO₂ in air) and lowest inthe Esthwaite plants (1–08 mol m^–3). Expressionof CAM in transplants was also greatest in the low CO₂ regime,with H⁺ (measured as dawn-dusk titratable acidity) of 50µmolg^– fr. wt., similar to Esthwaite plants in natural sediment.Assuming typical CAM stoichiometry, decarboxylation of malatecould account largely for the measured [CO₂]₁ and would makea major contribution to daytime CO₂ fixation in vivo. A range of leaf sections (0–2, 1–0, 5–0 and17–0 mm) was used to evaluate diffusion limitation andto select a suitable size for comparative studies of photosyntheticO₂ evolution. The longer leaf sections (17.0 mm), which weresealed and included the leaf tip, were diffusion-limited witha linear response to incremental addition of CO₂ and 1–0mol m^–3 exogenous CO₂ was required to saturate photosynthesis.Shorter leaf sections were less diffusion-limited, with thegreatest photosynthetic capacity (36 µmol O₂ g^–1 fr. wt. h^–1) obtainedfrom the 1.0 mm size and were not infiltrated by the incubatingmedium. Comparative studies with 1.0 mm sections from plants grown inthe different sediment types revealed that the photosyntheticcapacity of the sand-grown plants was greatest (45 µmolO₂ g^–1 fr. wt. h^–1) with a K_0.5 of 80 mmol m^–3.In terms of light response, saturation of photosynthesis intissue slices occurred at 850–1000 µmol m^–2s^–1 although light compensation points (6–11 µmolm^–2s^–1) and chlorophyll a: b ratios (1.3) were low.While CO₂ and PAR responses were obtained using varying numbersof sections with a constant fresh weight, the relationshipsbetween photosynthetic capacity and CO₂ supply or PAR were maintainedwhen the data were expressed on a chlorophyll basis. It is concludedthat under low PAR, CO₂ concentrating mechanisms interact inintact plants to maintain saturating CO₂ levels within leaflacunae, although the responses of the various components ofCO₂ supply to PAR require further investigation. Key words: Key words-Uttorella uniflora, internal CO₂ concentration, crassulacean acid metabolism, root inorganic carbon supply, CO₂ concentrating mechanism     

Comparisons of the Respiratory Effluxes of Nodules and Roots in Six Temperate Legumes

The specific respiration rates of nodulated root systems, ofnodules and of roots were determined during active nitrogenfixation in soya bean, navy bean, pea, lucerne, red clover andwhite clover, by measurements on whole plants before and afterthe removal of nodule populations. Similar measurements weremade on comparable populations of the six legumes, lacking nodulesbut receiving abundant nitrate-nitrogen, to determine the specificrespiration of their roots. All plants were grown in a controlled-environmentclimate which fostered rapid growth. The specific respiration rates of nodulated root systems ofthe three grain and three forage legumes during a 7–14-dayperiod of vegetative growth varied between 10 and 17 mg CO₂g^–1 (dry weight) h^–1. This mean value consistedof two components: a specific root respiration rate of 6–9mg CO₂ g^–1 h^–1 and a specific nodule respirationrate of 22–46 mg CO₂ g^–1 h^–1. Nodule respirationaccounted for 42–70 per cent of nodulated root respiration;nodule weight accounted for 12–40 per cent of nodulatedroot weight. The specific respiration rates of roots lackingnodules and utilizing nitrate nitrogen were generally 20–30per cent greater than the equivalent rates of roots from nodulatedplants. The measured respiratory effluxes are discussed in thecontext of nitrogen nitrogen fixation, nitrate assimilation. Glycine max, Phaseolus vulgaris, Pisum sativum, Medicago sativa, Trifolium pratense, Trifolium repens, soya bean, navy bean, pea, lucerne, red clover, white clover, nodule respiration, root respiration, fixation, nitrate assimilation     

Phosphate Uptake in the Cyanobacterium Synechococcus R-2 PCC 7942

Phosphate uptake rates in Synechococcus R-2 in BG-11 media (anitrate-based medium, not phosphate limited) were measured usingcells grown semi-continuously and in continuous culture. Netuptake of phosphate is proportional to external concentration.Growing cells at pH_o 10 have a net uptake rate of about 600pmol m^–2 s^–1 phosphate, but the isotopic flux for³²P phosphate was about 4 nmol m^–2 s^–1. There appearsto be a constitutive over-capacity for phosphate uptake. TheK_m and V_max, of the saturable component were not significantlydifferent at pH_o 7.5 and 10, hence the transport system probablyrecognizes both H₂PO^–₄and HPO^2–₄. The intracellularinorganic phosphate concentration is about 3 to 10 mol m^–3,but there is an intracellular polyphosphate store of about 400mol m^–3. Intracellular inorganic phosphate is 25 to 50kJ mol^–1 from electrochemical equilibrium in both thelight and dark and at pH_o 7.5 and 10. Phosphate uptake is veryslow in the dark ( 100 pmol m^–2 s^–1) and is light-activated(pH_o 7.51.3 nmol m^–2 s^–1, pH_o 10600 pmol m^–2s^–1). Uptake has an irreversible requirement for Mg²⁺in the medium. Uptake in the light is strongly Na⁺-dependent.Phosphate uptake was negatively electrogenic (net negative chargetaken up when transporting phosphate) at pH_o 7.5, but positivelyelectrogenic at pH_o 10. This seems to exclude a sodium motiveforce driven mechanism. An ATP-driven phosphate uptake mechanismneeds to have a stoichiometry of one phosphate taken up perATP (1 PO_{4 in}/ATP) to be thermodynamically possible under allthe conditions tested in the present study. (Received June 16, 1997; Accepted September 4, 1997)