Resistance to CO2 Fixation in the Submerged Aquatic Macrophyte Callitriche stagnalis Scop

The resistance to the photosynthetic carbon fixation in thefreshwater angiospcrm Callitriche stagnalis Scop was investigatedby gas exchange experiments in a closed water-flow system. Anelectrical analogue model was used to analyse uptake of carbonin terms of boundary layer resistance, cytoplasmic resistanceand carboxylation resistance. The most important rate-limitingfactor was the boundary layer resistance which was from 86%to 91 % of the total resistance of 852–1221 s cm^–1.The cytoplasmic and carboxylation resistances during activephotosynthesis were of minor importance being 89 s cm^–1and 24–30 s cm^–1, respectively. The calculated thicknessof the boundary layer surrounding the foliage of the shootswas 103–155 µm or 2–3 times the total thicknessof the leaves. The physiological and morphological characteristicsof submerged aquatic macrophytes are discussed as adaptationsto the low availability of carbon due to the high boundary layerresistance. Key words: Aquatic macrophytes, Resistance to carbon fixation, Adaptations     

Effects of algal concentration, bacterial size and water chemistry on the ingestion of natural bacteria by cladocerans

Journal of Plankton Research, 11, 1273–1295, 1989. The values of P/U⁰ (Table I) and fluid velocity used to calculatethe energy required for sieving (pp. 1289–1290) and severalequations (footnote b of Table I; p. 1290, lines 3–4)are incorrect. The corrected table appears below: Table I. Filter setule measurements (mean and within specimenstandard deviation) of the gnathobases for the cladocerans studied^aGnathobaseof trunklimb number. ^bP = 8µU₀/(b(1 – 21nt + 1/6(t²) - 1/144(t⁴))), whereP = pressure drop in dyn cm^–2, =3.1416, U₀ = fluid velocityin cm s^–1, b = distance between setule centres in cm,t = ( x setule diameter)/b and µ = 0.0101 dyn s^–1cm^–2. Formula from Jørgensen (1983). The text (p. 1289, line 19 to p. 1290, line 10) should read: organism. Using a similar argument, a 0.5 mm Ceriodaphnia witha filter area of 0.025 mm² (Ganf and Shiel, 1985) and pressuredrop P = 2757 dyn cm^–2 (with fluid velocity of 0.07 cms^–1) allocates only 2171 ergs h^–1 to filtrationof a total energy expenditure of 10⁴ ergs h^–1 [filtrationenergy (ergs h^–1) = area (cm²) x pressure drop (dyn cm^–2)x 3600 (s h^–1) x 1/0.2 (efficiency of conversion of biochemicalinto mechanical work); total energy (ergs h^–1) = respiration(0.05 µl O₂ ind^–1 h^–1 consumed; Gophen, 1976)x conversion factor (2 x 10⁵ ergs µl^–1 O₂). Withan estimated 0.034 mm² in filter area, fluid velocity of 0.041cm s^–1 and respiration of 1.8 x 10⁴ ergs h^–1 (calculatedfrom Porter and McDonough, 1984), a 0.5 mm Bosmina uses <4%of its metabolism to overcome filter resistance. The velocities used in the original examples (0.4 cm s^–1for Ceriodaphnia, 0.2 cm s^–1 for Bosmina) were derivedfrom literature values of appendage beat rate and estimatesof the distance travelled by the appendages during each beatcycle. This approach unnecessarily assumes that all water movedpasses through the filter. In the new calculations, the flowacross the filter needed for food to be collected by sieving(0.07 cm s^–1 for Ceriodaphnia and 0.041 cm s^–1 forBosmina) was determined from the maximum clearance rate/filterarea. The amended energy expenditures, although higher, do notrefute the sieve model of particle collection.     

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.     

Studies on the Movement of Water Through Apple Trees

Resistances to the flow of water through young potted appletrees were estimated by measuring the transpiration rate oftrees with and without root systems. Root system resistanceswere obtained by difference. Whole-plant resistances were ofthe order 10 x 10¹³ Pa s m^–3 and there was some evidencethat root resistances (R_r) varied with transpiration rate; theratio R_r:R_x (where R_x is resistance to water flow in the stemsystem) altered from 2:1 at relatively high transpiration ratesto 1:1 at lower rates. The trunk of a 9-year-old orchard tree (trunk diameter {smalltilde}7 cm, height {small tilde}2.5 m) was cut under water andestimates of the flow resistances in this tree were obtained.These were much lower than the resistances to flow in the pottedtrees. Capacitance (defined as the change in stored water content perunit change in plant water potential) values were calculatedfor the small trees and the large tree from measurements ofweight and water potential changes after the trees were removedfrom water. They were very similar on a weight basis (approx.2.0 x 10^–8 kg kg^–1 Pa^–1). Leaf capacitancevalues ({small tilde}1 x 10^–8 kg Pa^–1 m^–2)were also obtained. Stomatal conductances decreased with water potential and increasedwith short-wave radiation, but the relationships were not definitive.Estimates of boundary layer conductance in a greenhouse (verylow wind speeds) were of the same order ({small tilde}5 mm s^–1)as values obtained previously.     

Effect of Water Stress on Gas Exchange in Fronds of the Ostrich Fern (Matteuccia struthiopteris (L.) Todaro)

Experiments were conducted in a gas exchange system to examinethe effect of a water stress, induced by –200 kPa polyethyleneglycol (PEG), on carbon dioxide and water vapour flux, fronddiffusive resistance, intercellular carbon dioxide concentration,carbon dioxide residual resistance and frond water potentialin the ostrich fern (Matteuccia struthiopteris (L.) Todaro).Measurements were taken 1 d after the application of PEG. Themeasurements were made on young fronds (8 d old) and maturefronds (20–24 d old) at PPFD's (Photosynthetic PhotonFlux Density) from 0–1400 µmol m^–22 s^–1.Water stress decreased the net photosynthesis rate in maturefronds at PPFD's of 210 µmol m^–2 s^–1 or greaterand increased the net photosynthesis rate below 210 µmolm^–2 s^–1 in young fronds. The increase in net photosynthesisin stressed young fronds was associated with a significant reductionin the dark respiration rate. Water stress and decreasing PPFD'sincreased frond diffusive resistance. Carbon dioxide concentrationin the intercellular spaces decreased with increasing frondage and PPFD's up to 200 µmol m^–2 s^–1. Theresidual resistance to carbon dioxide flux was not significantlyaffected by either frond age or water stress. Frond water potentialwas significantly lower in mature fronds than in young fronds. Key words: Matteuccia struthiopteris, Water relations, Photosynthesis, Dark respiration     

Some Experimental and Theoretical Observations Concerning Mass Flow in the Vascular Bundles of Heracleum

The theory and practice of applying the thermodynamics of irreversibleprocesses to mass-flow theories is presented. Onsager coefficientswere measured on cut and uncut phloem and cut xylem strandsof Heracleum muntegazzimum. In 0.3 N sucrose + 1 mN KC1 theyare as follows. In phloem, L_EE = 5 ? 10–⁴ mho cm^–1,L_pE = 9 ? 10^–6 cm³ s^–1 cm^–2 volt^–1 cm,and L_PP = 0.16 cm³ s^–1 cm^–2 (J cm^–3)^–1cm. In uncut phloem strands L_EE is about 1 ? 10^–3 mhocm^–1. In xylem in 2 x 10^–3 N KCI, L_pp = 50 to 225,L_PE = 2 ? 10^–4, and L^EE = 4 ? 10^–3. The measurementsare tentative since the blockage of the sieve plates is an interferingfactor, but if they are valid they lead to the conclusion thatneither a pressure-flow nor an electro-kinetic mechanism envisaginga ‘long distance’ current pathway can be the majormotive ‘force’ for transport in mature phloem. Measurementsof biopotentials along conducting but laterally detached phloembundles of Heracleum suggest, nevertheless, that there may bea small electro-osmotic component of at least 0.1 mV cm^–1endogenous in the phloem.     

On the light and temperature dependence of the minimum and maximum phosphorus contents in cells of the marine plankton diatom Thalassiosira rotula Meunier

The thesis that the minimum cell-phosphorus content of planktonalgae is a light- and temperature-independent species constantwas investigated using the marine plankton diatom Thalassiosirarotula. To what extent the maximum cell-phosphorus content isalso a constant, light- and temperature-independent quantityhas been tested in parallel. At 2.5C and 3.03 nE cm^–2s^–1 the minimum and maximum cell-phosphorus contents aregreater than the values for 16C and 8.93 nE cm^–2 s^–1by a factor of 5.7. The light intensities were kept near thelight saturation for the growth rate for all experimental temperatures(2.5, 6, 12 and 16C). The light dependence of the phosphoruscontent was tested at 12C. For 1.43 nE cm^–2 s^–1the minimum phosphorus content was lower by a factor of 2.5than for 64.28 and 80.36 nE cm^–2 s^–1 respectively.The maximum P-content for 2.86 nE cm^–2 s^–1 was 3.9times higher than for 64.28 nE cm^–2 s^–1 T. rotulais, on the basis of the stored P-content, only capable of betweenthree and five cell divisions. The N/P atomic ratios were, dependingupon light and temperature, between 56:1 and 226:1 for the minimumcell-phosphorus content, which implies a pronounced phosphorusdeficiency.     

The Boundary Layer over a Populus Leaf

Air flow over a Populus leaf was investigated using a hot-wireanemometer. When the air flow in the wind tunnel was laminar,the boundary layer was often turbulent at a wind speed of only1.5 m s^–1, particularly when encouraged by uneven topographyand roughness of the surface, as on the lower side of the leaf.The smoother upper surface behaved in a similar way to a flatplate when at low wind speeds, and the profiles of wind speedcould be shown to be equivalent to those expected from laminarboundary layer theory. Nevertheless, the boundary layer becameturbulent at Reynolds numbers much lower than those requiredto cause the transition to turbulence in a flat plate. Turbulentair flow in the wind tunnel greatly increased boundary layerturbulence but had only a small effect on evaporation from amodel of the leaf. The evaporation rates observed were 2.5 timeshigher than expected from theory, irrespective of the turbulenceregime.     

Resistance to Water Loss in the Mesophyll of Leek (Allium porruni)

Measurement of the rate of water loss and the gradient in water-vapourconcentration from the evaporating surface to the air enabledcalculation of the resistance to water loss from the leaf mesophyllof leek (Allium porruni) and from green blotting-paper. Theadditional resistance found in the case of mesophyll estimatesthe mesophyll cell-wall resistance (wall resistance). Wall resistancewas, however, small, less than 0.09 sec cm^–1 in turgidmesophyll and only 0.15 sec cm^–1 greater when the mesophyllwater deficit was 50 per cent. Results are discussed in relationto the evidence of other workers indicating greater resistancesto water loss in the mesophyll.     

In-Phase Cycling of Photosynthesis and Conductance at Saturating Carbon Dioxide Pressure Induced by Increases in Water Vapour Pressure Deficit

Bunce, J. A. 1987. In-phase cycling of photosynthesis and conductanceat saturating carbon dioxide pressure induced by increases inwater vapour pressure deficit.—J. exp. Bot. 38: 1413–1420. The leaf to air water vapour deficit was increased suddenlyfrom about 1·0 to 2·5 IcPa for single leaves ofsoybean (Glycine max L. Merr.) plants held at 30 °C, 2·0mmol m ^–2 s^–1 photosynthetic photon flux density(PPFD) and carbon dioxide pressures saturating to photosynthesis.After a lag of about 10 min, photosynthetic rate and stomatalconductance to water vapour began to decrease, and then cycledin phase with each other. The period of the cydes was about20 min. During these cycles the substomatal carbon dioxide pressurewas constant in the majority of leaves examined, and was alwaysabove saturation for photosynthesis. Epidermal impressions showedthat most stomata changed in aperture during the cycles, andthat very few were ever fully closed. Water potential measuredon excised discs changed by at most 0·1 MPa from theminima to the maxima in transpiration rate. In contrast, forleaves of sunflower (Helianthus animus L.) grown at low PPFD,the increase in VPD led to leaf wilting and decreased photosynthesis,followed by recovery of turgor and photosynthesis as stomatalconductance began to decrease. In these leaves photosynthesisand conductance then cycled approximately 180° out of phase.It is suggested that in soybeans decreased leaf conductanceinduced by high VPD provided a signal which decreased the rateof photosynthesis at carbon dioxide saturation by a mechanismthat was not related to a water deficit in the mesophyll. Key words: Photosynthesis, stomatal conductance, cycling, vapour pressure deficit     

Dispersion characteristics of two planktonic diatoms

Not all phyloplankton behave as ideal water tracers. Longitudinaldispersion experiments were conducted in a large flume withseawater of constant depth and velocity. The transport of thepassive, fluorescent tracer, Rhodamine B dye, was compared withunialgal cultures of a large, fast-sinking diatom (Odontellachinensis) and a small, slow-sinking diatom (Skeletonema costatum).Horizontal dispersion rates, proportional to variance per distance,were linear for the dye and Skeletonema but nonlinear for Odontella.Results are explained by the interaction of Odontella sinkingand advection. Longitudinal dispersion coefficients for thedye and Skeletonema were between 60–80 cm² s^–1 andas high as 280 cm² s^–1 for Odontella. This may have implicationsfor nutrient uptake in natural phytoplankton populations.     

The Diffusive Conductivity of the Stomata of Wheat Leaves

A leaf chamber (described in detail) was used alternately witha resistance porometer to measure resistance to viscous flowof air through the leaf, and with a diffusion porometer to measurethe differential diffusive flow of hydrogen and air (V_H–V_A)through the leaf and the component of hydrogen flow (V'_H) movingstraight across the leaf. The resistance of the mesophyll isneeded for interpretation: estimates by three different methodsfor viscous flow did not agree very well, but two differentmethods for diffusive flow gave good agreement. For wheat leaves,only very large errors are important. Formal analysis is in three appendixes: I. Interpretation ofviscous and diffusive flow in small pores involves some problemsin molecular physics, complicated by the particular geometryof the wheat stoma. With some uncertainty, formal expressionsare derived for the viscous resistance of a single stoma, rv,and for the resistances to diffusion of hydrogen and air, andof water vapour and carbon dioxide, all expressed as r_s persquare centimetre of leaf surface. The analysis for hydrogen/airis the most uncertain; that for water vapour and carbon dioxideis more reliable. II. An indication is given of the flow characteristicsof the leaf-chamber system, from which rv can be derived, andof the basis for estimating mesophyll resistance. III. The methodof converting estimates of r_s into estimates of V_H–V_Aand V'_H is given. The results presented are expressed as nearly as possible interms of the quantities which were measured. For five leavesthe dependence of V_H–V_A on V'_H agrees well with theoreticalpredictions; the dependence of V_H–V_A (and V'_H) on rv,on average, agrees well with prediction, but involves the assumptionthat the stomata get shorter as they close. The agreement isgood enough to suggest that the formal expressions for r_s interms of stomatal dimensions and molecular gas constants arereliable enough to be carried forward into future transpirationand assimilation studies. The minimum value of ra for watervapour (c. 3 sec cm⁺¹) is close to values found elsewhere bydifferent techniques. At very small stomatal openings there was a large deviationfrom predicted behaviour, such as would occur if the imposedexcess air pressure further closed the stomata during viscousflow experiments.     

Growth of Ceratium hirundinella in a subtropical Australian reservoir: the role of vertical migration

A study into the photophysiology, growth and migration of Ceratiumhirundinella in Chaffey Reservoir in subtropical northern NewSouth Wales, Australia, revealed that a proportion of cellsformed subsurface accumulations at depths that optimized lightintensity (212–552 µmol photons m^–2 s^–1)for photosynthesis and cell growth. At high incident irradiance,Ceratium migrated downwards from the near-surface waters, avoidinghigh-light-induced, slow-recovering non-photochemical quenchingof photosystem II. Overnight deepening of the surface mixedlayer by convective cooling produced homogeneous distributionsof Ceratium with a significant proportion of the populationbelow the depth where light saturation of photosynthesis occurred.Ceratium migrated towards the surface from suboptimal lightintensities, at a velocity of 1.6–2.7 x 10^–4 m s^–1.Subsurface accumulations occurred under a variety of turbulenceintensities; however, accumulation was significantly reducedwhen the turbulent velocity scale in the mixed layer was >5x 10^–3 m s^–1, beyond which turbulent diffusion dominatedadvection by swimming. The formation of subsurface accumulationswith increased computed water column integral photosynthesisby 35% compared to a uniform cell distribution.     

Occurrence of viable photoautotrophic picoplankton in the aphotic zone of Lake Biwa, Japan

The distribution and abundance of photoautotrophic picoplankton(PPP. Synechococcus group) in the aphotic bottom sediments ofLake Biwa were investigated by direct counting and viable counting(most probable number, MPN) methods. In the surface layer ofbottom sediments (0–1 cm). where large PPP blooms occurredin the past 5 years, >10⁵ cells cm^–3 of PPP were foundto be viable throughout the year. Furthermore, the density ofPPP deposited on the sediment surface (0–0.1 cm) was oneorder of magnitude higher (MPN = 1.3 x 10⁶ cells cm^–3.direct count = 9.9 x 10⁶ cells cm^–3) than that of bulkedsurface sediments (0–1 cm). Even in the deeper layer (13–14cm) of bottom mud, viable PPP were still found (10¹ cells cm^–1.In winter, viable PPP in the aphotic bottom sediments were 10⁴–10⁵times greater per Unit volume than those in the euphotic lakewater. Since the aphotic bottom sediments have high levels ofPPP, as well as high growth potential (high ratio of viablecount/total direct count), they are likely to seed PPP bloomsin the North Basin of Lake Biwa.     

A System for Measuring Effects of Sulphur Dioxide on Gas Exchange of Plants

Apparatus is described for exposing plants to low concentrationsof SO₂ (50–500µg m^–3 in air) and for measuringeffects on photosynthesis, dark respiration, and transpiration.Temperature, humidity, and irradiance in the chambers were controlledindependently, and fans ensured that leaf boundary layer resistanceswere low. Experiments with plants of Vicia faba in clean andpolluted air showed that: (i) a depression of net photosynthesisby 50 µg m^–3 SO₂ depended on boundary layer resistanceand on irradiance; (ii) stomatal resistance was increased ordecreased by 50 µg m^–3 SO₂ when relative humidityin the chambers was low (35% r.h., 22 °C) or high (50% r.h.,22 °C) respectively.     

Size, composition and distribution of particles related to wind induced resuspension in a shallow tropical lagoon

The size, composition and distribution of particles in the watercolumn were surveyed in a shallow area (1 m depth) of a tropicallagoon (Cte d'Ivoire) during a sequence of wind-induced resuspension.Water samples were collected hourly near the surface duringone tidal cycle. Three characteristic periods were distinguished:a calm period with low wind speed (average 1.2 m s^–1 awindy period with wind speed >3 m^–1 s (range between4 and 6 m s^–1) inducing sediment resuspension and a relaxationperiod during the decrease of wind velocity. From the analysisof several parameters (particle size and volume, bacteria. pico-and nanophytoplankton, ciliates and detritus), sediment resuspensioncaused a regular injection of particles from the bed. The finestparticles (1.5–6 µm: chlorophytes such as Chiorellaspp., picocyanobacteria such as Synechococcus) were the firstto be affected by wind-induced turbulence, whereas large particles(6–12 µm: diatoms. cyanobacteria such as Lyngbiaspp.) were dispersed into the water column at the highest windspeed. The fate of the different seston components differedaccording to their size. Therefore, wind-induced resuspensioncould greatly influence the food web organization through thequantity, quality and size of edible particles available ata given time.     

Field Measurements of the Gas Exchange of Woody Plant Species in Simulated Sunflecks

The photosynthetic responses of eight tree and shrub speciesto simulated sunflecks was measured in the field. The net carbonexchange (NCE) of Corylus avellana and Ulmus glabra increasedwith irradiance up to the maximum irradiance of 230 µmolm^–2 s^–1. The NCE of Fraxinux excelsior, Hedera helixand the sun and shade forms of Rhododendron ponticum saturatedat about 120 µmol m^–2 s^–1 whereas the NCEof Ilex aquifolium, Daphne laureola and Fagus sylvatica hadeffectively saturated at 27 µmol m^–2 s^–1. In all cases the quantum efficiency of NCE could be predictedfrom measurements of chlorophyll fluorescence and the maximumvalue for NCE from measurements of stomatal conductance. Therelationships were combined into a model for predicting NCE/irradiancecharacteristics. Corylus avellana L., Daphne laureola L., Fagus sylvatica L., Fraxinus excelsior L., Hedera helix L., Ilex aquifolium L., Prunus laurocerasus L., Rhododendron ponticum L., Ulmus glabra Huds., gas exchange, stomatal resistance, water use efficiency, chlorophyll fluorescence, quantum efficiency     

A Method for Separating Cuticular and Stomatal Components of Gas Exchange by Amphistomatous Leaves: II. EXPERIMENTAL SOLUTION

The apparent cuticular component of transpiration of stomatabearing leaf epidermis was estimated by restricting stomataldiffusion by mass flow of air in the opposite direction. Thiswas achieved by applying an air pressure gradient across theamphistomatous leaf. Some assumptions of the previously suggestedmethod (antrcek and Slav?k, 1990) were experimentally verifiedusing maize leaves. The technique makes possible a quantitativeestimation of cuticular water loss including that of the externalperistomatal (i.e. vapour not passing through the pores) andthe respective conductance when the stomata are partially open. In addition to the fact that the cuticular portion of the totalleaf vapour loss (i.e. relative cuticular transpiration) dependson stomatal opening, even the absolute value of apparent cuticulartranspiration was (1) increased by lower vapour pressure deficitand (2) decreased with closing stomata. These changes, inducedby variations in a vapour pressure deficit of 2.45?0.35 kPa,ranged between 0.66?0.14µg cm ^–2 s^–1. Theabsolute value of apparent cuticular transpiration changed onaverage by a factor of 2.3 due to stomata opening or closingwhich was induced by turning the light on or by exogenous ABAapplication. Possible interference by residual vapour diffusingthrough the stomatal pore was evaluated by the model application.An attempt was also made to assess the cuticular component ofCO₂-uptake rate. Experimental results are discussed in contextwith the feedforward response of stomata to air humidity. Key words: Cuticular transpiration, cuticular CO₂-uptake, feedforward response, maize     

The Effect of Wind on Grasses: 1. CUTICULAR AND STOMATAL TRANSPIRATION

Transpiration of Festuca arundinacea Schreb, strain S170, wasmeasured at two different wind speeds in a controlled-environmentwind tunnel. As a result of a wind increase from 1 m s^–1to 3.5 m s^–1 above the sward, transpiration graduallyincreased, especially at night-time. Similar effects were notedin three other grass species. The transpiration increase couldbe attributed to decreases in stomatal and cuticular resistances,as a result of leaf buffeting.     

Stomatal Control of Photosynthesis of Eucalyptus globulus Labill. Trees under Field Conditions in Portugal

Pereira, J. S., Tenhunen, J. D. and Lange, O. L. 1987. Stomatalcontrol of photosynthesis of Eucalyptus globulus Labill. treesunder field conditions in Portugal.—J. exp. Bot. 38: 1678–1688. Stomatal behaviour of adult leaves of Eucalyptus globulus treeswas studied under field conditions in Portugal. In the absenceof severe plant water stress stomata were open when the summedtotal of photosynthetically active photon flux density incidenton both leaf surfaces was above 100 µmol m²s¹ and leafconductance to water vapour reached 245 mmol m ² s¹ on a total(both epidermes) leaf area basis. The stomata of both leaf epidermesresponded similarly to changes in solar radiation and waterstress. Water stress resulted in decreasing daily maxima inleaf conductance as predawn leaf water potential decreased.Maximal leaf conductance decreased to less than 50 mmol m ²s ¹ when predawn leaf water potential decreased below —1·0MPa. At similar values of predawn leaf water potential stomatawere more closed as the leaf to air water vapour partial pressuredifference increased. The effect of increasing air dryness onstomata was greatest at high predawn leaf water potential. Dailymaxima in photosynthetic rates and in leaf conductance werelinearly related to one another in spring and summer. Both decreasedwith increase in leaf water stress. In autumn and winter, increasesin leaf conductance occurring under natural conditions duringthe course of the day were not necessarily accompanied by increasesin net photosynthesis. Stomata were more closed in the afternoonthan in the morning at the same rates of net photosynthesis,temperature or leaf to air water vapour partial pressure difference. Key words: Eucalyptus globulus,, photosynthesis, stomata, water stress.