Respiratory electron transport system (ETS) activity as an estimator of the thermal tolerance of two Daphnia hybrids

The influence of temperature on the activity of the respiratoryelectron transport system (ETS) was measured in one clone ofDaphnia hyalina x galeata and one of Daphnia cucullata x galeata,isolated from Lake Bled (Slovenia). The ETS activity of ovigerousfemales acclimated to 7, 20 and 25°C, was measured at 5,10, 15, 20, 25 and 30°C. Population growth experiments showedthat D. cucullata x galeata grew better at high rather thanlow temperatures. Daphnia hyalina x galeata, however, grew moresuccessfully at low temperatures than did D. cucullata x galeata.The highest Q₁₀ of ETS activity of D. cucullata x galeata atthe lowest temperature range of 5–15°C indicated theabsence of enzymes that could function sufficiently well atlow temperatures. The ETS activity of the warm-acclimated hybridD. hyalina x galeata reached a maximum at an incubation temperatureof 20°C, while D. cucullata x galeata had maximal ETS activityat 25°C. Thus D. cucullata x galeata has a more efficientenzyme system than D. hyalina x galeata at the higher temperature.The higher Arrhenius activation energy (E_a) for D. cucullatax galeata than for D. hyalina x galeata indicates that enzymesfrom D. cucullata x galeata are more temperature sensitive thanthose from D. hyalina x galeata. In conclusion, the ETS of D.cucullata x galeata is adapted to a higher temperature and tonarrower temperature fluctuations than that of D. hyalina xgaleata.     

Competition Between Native and Exotic Daphnia: In situ Experiments

The recently introduced exotic cladoceran Daphnia lumholtzioffers an excellent opportunity to study the interactions betweenexotic and native species in invaded communities. Lake surveysin Missouri have indicated a seasonal succession between nativeDaphnia and D. lumholtzi. In the current study, we examinedcompetition between D. lumholtzi and the native Daphnia parvulaby conducting seasonal in situ field experiments in 1.6 l enclosures.Competition was assessed by comparing the rates of increase(r) and birth rates (b) of each species when grown alone versuswhen grown together in these enclosures. At high densities,D. lumholtzi suppressed D. parvula rates of increase duringthe late summer and fall experiments, but did not appear tosuppress D. parvula birth rates. The rates of increase of D.lumholtzi did not appear to be affected by the presence of D.parvula. The results of these experiments indicate that althoughcompetition between the two species occurs seasonally at highdensities, the effects are asymmetrical. The lack of competitiveeffects on D. lumholtzi byD. parvula suggests that factors otherthan competition are involved in explaining the absence ofD.lumholtzi in spring zooplankton assemblages.     

Invasibility of a reservoir to exotic Daphnia lumholtzi: experimental assessment of diet selection and life history responses to cyanobacteria

SUMMARY 1. In reservoirs of the south-central United States, the exotic cladoceran Daphnia lumholtzi is common during warm midsummer conditions, when cyanobacteria are abundant and native Daphnia are rare. In the current study, we employed surveys, field experiments, and a life table experiment to investigate the role of food quality in explaining the distribution and phenology of D. lumholtzi , relative to two native species ( Daphnia parvula and Daphnia mendotae ).
2. During May–September 2000 in eutrophic McDaniel Lake, Missouri U.S.A., cyanobacteria (primarily Oscillatoria ) first appeared at 6-m depth and then became abundant throughout the epilimnion.
3. During the May field experiment, D. lumholtzi , D. parvula and D. mendotae all consumed a similar diet of algae, showing positive selection for small greens (chlorophytes and cryptophytes <20 μm). During the July experiment, when the epilimnion exceeded 25 °C and cyanobacteria were common in the lake, D. lumholtzi consumed significantly more total algae and more cyanobacteria than the two native species. Although the Daphnia selected against cyanobacteria, all three species consumed about 25% of this food in their diet.
4. A life table experiment compared the responses of D. lumholtzi and D. parvula with variation in density of high-quality food ( Ankistrodesmus ) and concentration of a toxic strain of cyanobacteria ( Anabaena flos-aquae ). Both Daphnia species showed reduced survivorship, fertility and intrinsic rates of increase in response to elevated concentrations of cyanobacteria, particularly at the higher food level.
5. The results suggest that D. lumholtzi shows similar inhibition from cyanobacteria as does the native Daphnia . However, their continued high in situ feeding rates imply that D. lumholtzi is less affected by midsummer conditions in warm-water reservoirs than are native Daphnia .     

Predation by inland silversides on an exotic cladoceran, Daphnia lumholtzi, in Lake Texoma, U.S.A.

In the early 1990s, Lake Texoma was invaded by Daphnia lumholtzi , a large, spiny, exoticcladoceran. From April 1994 to April 1995 D. lumholtzi was most abundant in the lake in mid-summer, after native zooplankton declined in early June. Inland silversides Menidia beryllina selectively preyed on D. lumholtzi but appeared to prefer the large native zooplankton when they were present. Daphnia lumholtzi was an important prey item for silversides during summer when large native zooplankton was scarce. The invasion of D. lumholtzi into Lake Texoma may benefit some zooplanktivorous fishes by increasing foraging opportunities during a time of low prey availability.     

Range expansion and potential dispersal mechanisms of the exotic cladoceran Daphnia lumholtzi

. Recently the exotic cladoceran Daphnia lumholtzi has invadedfreshwater systems throughout the southern and midwestern UnitedStates. We conducted regional surveys of eastern Kansas reservoirsto document the range expansion of D.lumholtzi. Daphnia lumholtziwas found in five of 35 reservoirs sampled in 1994, and 11 ofthe 35 reservoirs when re-sampled in 1997. In addition, we sampled40 small ponds inaccessible to recreational boats, within thewatershed of an invaded reservoir. We did not find D.lumholtziin any of these ponds, suggesting that non-human dispersal mechanismsplay an insignificant role in the range expansion of D.lumholtzithroughout the United States. Further experimentation, however,is needed to determine if the absence of D.lumholtzi from thesesmall ponds is due to insufficient dispersal mechanisms or theinability of this invader to successfully colonize followingarrival. Daphnia lumholtzi has broad limnological tolerances.However, invaded reservoirs tend to be larger in area, havehigher Secchi disk depths, and lower total phosphorus, totalnitrogen and chlorophyll a levels relative to non-invaded reservoirs.Analyses of pre-invasion zooplankton communities indicate thatD.lumholtzi may be invading reservoirs in which native Daphniaspecies are rare. While the long-term effects of the invasionof D.lumholtzi are unknown, it has the potential to dominatelate summer zooplankton communities in eastern Kansas reservoirs.Therefore, we need to continue to survey and monitor invadedreservoirs to document the range expansion of D.lumholtzi anddetermine the long-term implications of the introduction ofthis invader.     

Factors which affect the abundance of an invasive cladoceran, Daphnia lumholtzi, in U.S. reservoirs

1.  Daphnia lumholtzi is a subtropical, Old World species which is rapidly spreading throughout reservoirs in the southern U.S.A. It was first recorded in Lake Texoma (Oklahoma–Texas) in September 1991.
2. Southern U.S. reservoirs typically have strong spatial and temporal gradients in temperature, conductivity, turbidity and in the distribution of organisms. Therefore, the present experiments examined the reproductive and moulting rates, and survival of D . lumholtzi in relation to extremes of food concentration, temperature, conductivity and turbidity.
3. Increases in temperature (range = 15–29 °C) and decreases in turbidity (range = 0.6–470 NTU) increased reproductive and moulting rates, whereas food concentration only affected the rate of reproduction, while conductivity had no effects. Survival was affected only by temperature.
4.  Daphnia lumholtzi tolerates high temperatures (27–30 °C) at which other cladocerans in Lake Texoma disappear. Therefore, D . lumholtzi may exploit resources in midsummer, when there are few potential competitors.     

Sink-Regulation of Photosynthesis in Relation to Temperature in Sunflower and Rape

Stimulation of the rate of photosynthesis at 2·0 kPaO₂ in comparison with 21 kPa O₂ and carbohydrate accumulationover 4h were measured during exposure of sunflower (Helianthusannuus L.) and rape (Brassica napus L.), grown at 30 °Cand 13 °C, to temperatures between 7 °C and 35 °C.The effect of reducing source: sink ratio by shading on theresponse of photosynthetic rate to temperature was also determined.Stimulation of photosynthesis by 2·0 kPa O₂ in comparisonwith 21 kPa O₂ decreased over 4 h at cool temperatures in sunflowerplants grown at 30 °C but not in rape grown at 30 °C.Stimulation did not decrease over 4 h in plants grown at 13CC. Sucrose was the main carbohydrate accumulated over 4 h;its accumulation increased with decreasing temperature. Starchaccumulation either decreased or remained the same with decreasingtemperature. In plants grown at 30 °C more carbohydrateaccumulated between 8 °C and 21 °C in sunflower thanin rape, but more carbohydrate accumulated at 30 °C in rapethan in sunflower. In plants grown at 13 °C much less carbohydrateaccumulated between 13 °C and 23 °C than in plants grownat 30 °C. Photosynthetic rate in plants grown at 30 °Cexposed to between 20 °C and 35 °C over 32 h (14 h light-10h dark-8 h light), declined over 32 h at 20 °C and 25 °Cin sunflower and at 20 °C in rape. This fall over 32 h,especially at 20 °C in sunflower, was significantly reducedby shading the rest of the plant. Shading had little effecton photosynthetic rate above 25 °C. The work confirms thatlow temperature imposes a sink-limitation on photosynthesiswhich occurs at higher temperatures in sunflower than in rape.This limitation may be relieved by decreasing the source:sinkratio. Key words: Sunflower, rape, photosynthesis, carbohydrates, sink demand, temperature     

Differing effects of suspended sediments on the performance of native and exotic Daphnia

1. Although large cladocerans are usually uncommon in large rivers, Daphnia lumholtzi (an exotic species in North America) is widespread and occasionally abundant. We collected zooplankton on the Illinois River (Illinois, U.S.A.) in 1995 and 1996 and found that the peak density of D. lumholtzi (25 L⁻¹) typically exceeded that of all native species combined. Maximum density occurred during warm periods (up to 27 °C) when concentrations of inorganic suspended sediments were high (>50 mg L⁻¹).
2. Using a life table experiment, we examined the effects of variation in suspended sediment (0 and 80 mg L⁻¹) and food (10⁴ and 10⁵ Ankistrodesmus cells mL⁻¹) on fitness of D. lumholtzi and the native Daphnia parvula. Daphnia lumholtzi had greater survivorship than D. parvula in most treatments and higher life-time fertility than D. parvula in all treatments. Both species achieved their fastest intrinsic rates of growth in treatments with high food, but their responses to suspended solids differed. The growth rate of D. lumholtzi in high food was slightly increased by higher turbidity, whereas that of D. parvula was depressed.
3. Results suggest that the ability of D. lumholtzi to tolerate suspended solids is an important factor contributing to its success in invading North American rivers.     

WATER EXCHANGE, TEMPERATURE TOLERANCE, OXYGEN CONSUMPTION AND ACTIVITY OF THE NAMIB DESERT SNAIL, TRIGONEPHRUS SP.

Water exchange, temperature tolerance and oxygen consumptionof the snail, Trigonephrus sp., from the southern Namib desertof Namibia were examined and related to activity. At 25°Cand 15% R.H. mean water loss and food and water uptake were5.95 mg. day^–1 and 630 mg.day^–1, respectively. Bodytemperature tracked sand temperature. Snails tolerated sandtemperatures as high as 45°C. Mean ± S.D. oxygenconsumption rates were 32.0 ± 2.94 µlO₂.g totalbody mass^–1.h^–1 at 15°C, when the snails wereactive, and 11.27 µlO₂.g total body mass^–1.h^–1at 25°C, when the snails were inactive. These values are2-6 times lower than those recorded for the similarly sizedmesic snail, Helix aspersa. Activity experiments indicated thatlow ambient temperatures and high humidities were favoured bythe snails. This, together with the burying behaviour of thesesnails during high temperatures, suggests that they limit stressby restricting activity to physiologically-favourable periods,even though more-extreme conditions may be tolerated. (Received 7 June 1990; accepted 20 November 1990)     

Effects of Temperature and Water Loss on Terrestrial Locomotor Performance in Land Crabs: Integrating Laboratory and Field Studies

SYNOPSIS. Terrestrial and semi-terrestrial crustaceans are exposedto fluctuations in ambient temperature and conditions that favorevaporative water loss. These environmental stresses alter performancelimits in the laboratory and behavior in the field. The maximalrate of oxygen consumption, maximum aerobic speed, and endurancecapacity are greater at a body temperature (T_b) of 24°Cthan at 15°C or 30°C in the ghost crab, Ocypode quadrata.The total metabolic cost to move at the same relative speedis greater at a T_b of 24°C than at 15°C. Slower aerobickinetics at 15°C result in a smaller relative contributionof oxidative metabolism to total metabolic cost. However, therelative contributions from accelerated glycolysis are similarat both temperatures. When locomotion is intermittent, the totaldistance traveled before fatigue can be similar at Tbs of 15and 24°C but result from different movement and pause durationsat these temperatures. Performance limits of the ghost crabare negatively affected by dehydration and are sensitive torates of water loss. In the laboratory, endurance capacity ofthe fiddler crab, Uca pugilator, is greater at a T_b of 30°Cthan at 25°C. In the field, freely moving fiddler crabswith a T_b of 30°C travel at faster mean preferred speeds,as determined by motion analysis, than crabs at 25°C. Datafor land crabs support and advance general ectothermic modelsfor the effects of temperature and dehydration on locomotorperformance.     

Concurrent Rates of N2 Fixation, Nitrate and Ammonium Uptake by White Clover in Response to Growth at Different Root Temperatures

Nodulated white clover plants (Trifolium repens L. cv. Huia)were grown for 71 d in flowing nutrient solutions containingN as 10 mmol m_–3 NH₄NO₃, under artificial illumination,with shoots at 20/15°C day/night temperatures and root temperaturereduced decrementally from 20 to 5°C. Root temperatureswere then changed to 3, 7, 9, 11, 13, 17 or 25°C, and theacquisition of N by N₂ fixation, NH₄+ and NO₃^– uptakewas measured over 14 d. Shoot specific growth rates (d. wt)doubled with increasing temperature between 7 and 17°C,whilst root specific growth rates showed little response; shoot:root ratios increased with root temperature, and over time at11°C. Net uptake of total N per plant (N₂ fixation + NH₄++ NO₃^–) over 14 d increased three-fold between 3 and 17°C.The proportion contributed by N₂ fixation decreased with increasingtemperature from 51% at 5°C to 18% at 25°C. Uptake ofNH₄+ as a proportion of NH₄+ + NO₃^– uptake over 14 d variedlittle (55–62%) with root temperature between 3 and 25°C,although it increased with time at most temperatures. Mean ratesof total N uptake per unit shoot f. wt over 14 d changed littlebetween 9 and 25°C, but decreased progressively with temperaturebelow 9°C, due to the decline in the rates of NH₄+ and NO₃^–uptake, even though N₂ fixation increased. The results suggestthat N₂ fixation in the presence of sustained low concentrationsof NH₄+ and NO₄^– is less sensitive to low root temperaturethan are either NH₄+ or NO₃^– uptake systems. White clover, Trifolium repens L. cv. Huia, root temperature, nitrogen fixation, ammonium, nitrate     

Thermal and metabolic responses to cold-water immersion at knee, hip, and shoulder levels

Lee, Dae T., Michael M. Toner, William D. McArdle, IoannisS. Vrabas, and Kent B. Pandolf. Thermal and metabolic responses tocold-water immersion at knee, hip, and shoulder levels.J. Appl. Physiol. 82(5):1523-1530, 1997.To examine the effect of cold-water immersion atdifferent depths on thermal and metabolic responses, eight men (25 yrold, 16% body fat) attempted 12 tests: immersed to the knee (K), hip(H), and shoulder (Sh) in 15 and 25°C water during both rest (R) orleg cycling [35% peak oxygen uptake; (E)] for up to 135 min. At 15°C, rectal (T_re)and esophageal temperatures(T_es) between R and E were notdifferent in Sh and H groups (P > 0.05), whereas both in K group were higher during E than R(P < 0.05). At 25°C,T_re was higher(P < 0.05) during E than R at alldepths, whereas T_es during E washigher than during R in H and K groups.T_re remained at control levels inK-E at 15°C, K-E at 25°C, and in H-E groups at 25°C,whereas T_es remained unchanged inK-E at 15°C, in K-R at 15°C, and in all 25°C conditions (P > 0.05). During R and E, themagnitude of T_re change wasgreater (P < 0.05) than themagnitude of T_es change in Sh andH groups, whereas it was not different in the K group(P > 0.05). Total heat flow wasprogressive with water depth. During R at 15 and 25°C, heatproduction was not increased in K and H groups from control level(P > 0.05) but it did increase in Shgroup (P < 0.05). The increase inheat production during E compared with R was smaller(P < 0.05) in Sh (121 ± 7 W/m² at 15°C and 97 ± 6 W/m² at 25°C) than in H (156 ± 6 and 126 ± 5 W/m²,respectively) and K groups (155 ± 4 and 165 ± 6 W/m², respectively). These datasuggest that T_re andT_es respond differently duringpartial cold-water immersion. In addition, water levels above knee in15°C and above hip in 25°C cause depression of internal temperatures mainly due to insufficient heat production offsetting heatloss even during light exercise.

     

A Temperature Effect on the Expression of Genotypic Differences in Flowering Induction in Antirrhinum majus

Three inbred lines of Antirrhinum majus and the F₁ generationsof crosses between them were scored for flowering time in ninegreenhouse and garden experiments. The inbreds fell into twogroups, the difference between which showed a marked interactionwith environments. The two lines (An 105, An 106) which weresimilar were earlier flowering than the third line (An 101)in those environments which produced generally early flowering,but were later than An 101 when the environmental conditionsled to late flowering. In all cases the F₁ generations wereat least as early as the earlier parent. Cabinet experiments identified temperature as the importantenvironmental factor when day length was kept constant at 16h. At 25°C, An 105 and An 106 were earlier than An 101 whileat 12°C, at which temperature the average flowering timewas much later, An 101 was earlier. The F₁ generations werelike An 105 and An 106 at 25°C but showed heterosis at 12°C. The differences in flowering time between genotypes were inall cases established by the time the first reproductive budsbecame visible (budding time). Thus a temperature differencewell outside the range of vernalizing temperatures is havinga striking effect on the phenotypic expression of genotypicdifferences determining the transition from vegetative to floweringdevelopment.     

Root Zone Temperature Effects on Growth and Nitrate Absorption in Rape (Brassica napus cv. Emerald)

Effects of root temperatures, ranging from 10–35 °C, on growth and nitrate inflow of fodder rape seedlings (cv.Emerald) were examined. These were cultured in solution, withtheir shoots held at 25 ° C. Nitrate inflow (uptake rateper unit root length) was little affected over the temperaturerange 10–30 ° C, although enhanced values were foundat 35 ° C. Nitrate absorption by roots at 10-30 ° Cdepleted solution concentrations to an apparent minimum of approximately6.0 µM NO₃^–. Relative growth rates were highestwith root temperatures of 25 ° C and 30 °C, and thesewere associated with the greatest nitrate depletion rates fromsolution. Root: shoot weight ratios were also greatest at 25°C and 30 °C. At 10 °C and 35 °C a relativelylarge shoot on a small root maintained nitrate inflow in spiteof the plants' slow growth rate. The nitrogen concentrationin the shoots was little affected by root temperature. Slowgrowth at a root temperature of 10 °C was not associatedwith a shortage of nitrogen in the shoots. The principal influenceof temperature appears to be on extension and differentiationof root tissues, possibly through effects on carbohydrate supplyto root meristems.     

The Effect of Temperature on the Respiration of 14C-Labelled Sugars in Stems of Willow

The leaves of willow cuttings were allowed to assimilate ¹⁴CO₂,and the rate of increase of activity in the sieve-tube sap,collected as aphid honeydew, was compared with the output ofrespiratory ¹⁴CO₂ from the stem at 25 °C and at 0 °C. In the case of 3–5-week-old young shoots, the relativerate of breakdown of the ¹⁴C-labelled sugars was reduced at0 °C as compared with 25 °C. With 2–4-year-oldmature stems, however, the rate of breakdown of labelled sugarsin transit through the phloem was increased at 0 °C relativeto that at 25 °C. When the labelled sugars were being respiredin isolated stem segments where no transport was taking place,then low temperatures markedly reduced the rate of breakdownin both young shoots and mature stems. These results are discussed in relation to the results of otherworkers who have studied temperature effects on sieve-tube transport.     

THE EFFECT OF ENVIRONMENTAL VARIABLES ON THE OXYGEN CONSUMPTION OF THE PROTOBRANCH BIVALVE NUCULA TURGIDA (LECKENBY AND MARSHALL)

The oxygen consumption of the protobranch bivalve Nucula turgidawas measured in relation to size and to variation in temperatureand ambient oxygen tension. The slope of the line relating logsize and log oxygen uptake varied from 0.539 to 0.884 over therange 5°C to 40°C in summer – conditioned (S)animals but for winter – conditioned (W) animals the slopevaried from 0.561 to 0.762 over the range 5°C to 15°Conly; from 20°C to 35°C the values for the slope fellfrom 0.298 to 0.092. There was evidence of reverse acclimation,since the absolute rate of oxygen consumption was greater inS animals than in W over the temperature range studied. Thelethal limit for both groups appeared to be between 30°Cand 35°C. At all temperatures (5°C–25°C) N. turgida wasfound to be a near complete oxyconformer with b₂ x 10³ valuesranging from +0.0754 to –0.0234. The responses to temperature differ little from those of eulamellibranchbivalves, but the lack of ability to oxyregulate does demonstratea difference which may be linked to the different gill structure. (Received 13 January 1983;     

A Comparative Study of the Influence of Salt Type and Concentration on 14CO2 Fixation in Potato Slices at 25{degrees} C and 0{degrees} C

Dark fixation of ¹⁴CO₂ was followed in potato disks under varyingsalt treatments at 0° C and 25° C. It is shown thatthe specific activity of the ¹⁴CO₂ supplied is heavily dilutedby endogenously produced CO₂ and that the apparently greaterfixation of ¹⁴CO₂, at 0° C as compared with that at 25 °C is due to the lower respiration rate at 0° C, with consequentlyless dilution of the ¹⁴CO₂. supplied. At 25° C organic acidformation in response to different salt treatments fulfils thecommon expectation, ¹⁴CO₂ fixation increasing in the presenceof K₂SO₄ and decreasing in CaCl₂ relative to that in KCl. Therole of organic acids in maintaining ionic balance within thecell at 25° C is thereby indicated but at 0° C organicacid adjustments did not follow the normal pattern. At 25°C but not at o° C increasing external concentration of KCIresulted in an increased level of ¹⁴CO₂ fixation.     

Developmental Physiology of Sugar-beet: IV. EFFECTS OF GROWTH SUBSTANCES AND DIFFERENTIAL ROOT AND SHOOT TEMPERATURES ON SUBSEQUENT GROWTH

The effects of three growth substances, viz. indol-3yl-aceticacid (IAA), gibberellic acid (GA₃), and kinetin (KIN), and differentialshoot and root temperatures on growth of sugar-beet (Beta vulgarisL.) plants have been studied. IAA, GA₃, and KIN were applied in aqueous lanolin at differentconcentrations (50 ppm to 5000 ppm) to decapitated sugar-beetplants at the eight-leaf stage, one group also having alternateleaves removed. The growth substances significantly increasedthe dry weights of the plants when all the leaves were present,which was mainly explained by the large increase in roots. Thegrowth substances probably stimulated cambial activity and hencethe mobilization of substrates resulting in a bigger root whena relatively large leaf area existed. The failure of the plantsto respond to treatments following the removal of alternateleaves suggests that under such conditions the growth substanceshave hardly any major effect on the production of substrates;rather they influence growth by regulating the movement of substratesby altering the ‘sink strength’ if the supply ofsubstrates is not limiting. It could also be that the rootsproduce sufficient growth substances to maintain half the leavesat maximum expansion and maximum photosynthesis. Treatment withgrowth substances would therefore have little effect. When allthe leaves were present, they are limited by insufficient growthsubstances. All combinations of root and shoot temperatures of 17 and 25°C were imposed on plants decapitated at the eight-leafstage, one group also having each alternate leaf removed. Leaf8 expanded most at shoot and root temperature of 25 °C whereasother leaves had the largest areas at shoot and root temperatureof 17 °. When all the leaves were present root growth wasmaximal at shoot temperature of 17°C and root temperatureof 25 °C, but when alternate leaves were removed maximumroot growth occurred at shoot and root temperatures of 25 °C.Generally, a higher concentration of soluble carbohydrates wasfound in the roots and leaves when either the shoot or rootor both were kept at 17 °C. Concentrations of nitrogen,phosphorus, and potassium in different organs were less at 17°C than at higher shoot or root temperatures and decreasedwith age.     

Transpiration and Photosynthesis in Soybean: EFFECTS OF TEMPERATURE AND VAPOUR PRESSURE DEFICIT

Continuous and simultaneous measurements of CO₂ exchange andtranspiration rates of whole soybean plants were made undercontrasting, controlled environmental conditions for periodsof up to 3 d. Daytime temperatures and vapour pressure deficits(VPD) were 27.5 °C/12 mb; 27.5 °C/5 mb; 22.5 °C/12mb, and 22.5 °C/5 mb. Night temperatures were 5°C lowerthan day temperatures and night VPD was 2.7 mb and 3.5 mb atthe higher and lower temperature respectively. The experimentalconditions were virtually the same as those under which theplants had been grown. Transpiration rates were higher at the higher VPD but were alsoinfluenced by temperature. At 12 mb VPD the rates were 16 percent lower at 22.5 °C than at 27.5 °C. Temperature hadno effect on the transpiration rate at 5 mb VPD. Photosynthesis rates were lower at 5 mb VPD than at 12 mb VPDat both temperatures: the difference was substantially greater(c. 70 per cent) at 22.5 °C. Under all treatments meso-phyllresistance (r'_m) appeared to have a major effect on the photosyntheticrate, and varied more than twofold between treatments. r'_m washighest in plants grown at 22.5 °C/5 mb VPD and lowest at27.5 °C/12 mb VPD.