Salt stress and fluctuating light have separate effects on photosynthetic acclimation,but interactively affect biomass

In nature, soil salinity and fluctuating light (FL) often occur concomitantly. However, it is unknown whether salt stress interacts with FL on leaf photosynthesis, architecture, biochemistry, pigmentation, mineral concentrations, as well as whole-plant biomass. To elucidate this, tomato (Solanum lycopersicum) seedlings were grown under constant light (C, 200 μmol m⁻² s⁻¹) or FL (5–650 μmol m⁻² s⁻¹), in combination with no (0 mM NaCl) or moderate (80 mM NaCl) salinity, for 14 days, at identical photoperiods and daily light integrals. FL and salt stress had separate effects on leaf anatomy, biochemistry and photosynthetic capacity: FL reduced leaf thickness as well as nitrogen, chlorophyll and carotenoid contents per unit leaf area, but rarely affected steady-state and dynamic photosynthetic properties along with abundance of key proteins in the electron transport chain. Salt stress, meanwhile, mainly disorganized chloroplast grana stacking, reduced stomatal density, size and aperture as well as photosynthetic capacity. Plant biomass was affected interactively by light regime and salt stress: FL reduced biomass in salt stressed plants by 17%, but it did not affect biomass of non-stressed plants. Our results stress the importance of considering FL when inferring effects of salt-stress on photosynthesis and productivity under fluctuating light intensities.     

Salinity effect on plant growth and leaf demography of the mangrove, Avicennia germinans L.

We assessed the effect of salinity on plant growth and leaf expansion rates, as well as the leaf life span and the dynamics of leaf production and mortality in seedlings of Avicennia germinans L. grown at 0, 170, 430, 680, and 940 mol m⁻³ NaCl. The relative growth rates (RGR) after 27 weeks reached a maximum (10.4 mg g⁻¹ d⁻¹) in 170 mol m⁻³ NaCl and decreased by 47 and 44% in plants grown at 680 and 940 mol m⁻³ NaCl. The relative leaf expansion rate (RLER) was maximal at 170 mol m⁻³ NaCl (120 cm m⁻² d⁻¹) and decreased by 57 and 52% in plants grown at 680 and 940 mol m⁻³ NaCl, respectively. In the same manner as RGR and RLER, the leaf production (P) and leaf death (D) decreased in 81 and 67% when salinity increased from 170 to 940 mol m⁻³ NaCl, respectively. Since the decrease in P with salinity was more pronounced than the decrease in D, the net accumulation of leaves per plant decreased with salinity. Additionally, an evident increase in annual mortality rates (λ) and death probability was observed with salinity. Leaf half-life (t _0.5) was 425 days in plants grown at 0 mol m⁻³ NaCl, and decreased to 75 days at 940 mol m⁻³ NaCl. Thus, increasing salinity caused an increase in mortality rate whereas production of new leaves and leaf longevity decreased and, finally, the leaf area was reduced.     

Effect of assimilate utilization on photosynthetic rate in wheat

Summary Two weeks after anthesis, when the grain is filling rapidly, the rate of photosynthesis by flag leaves of wheat cv. Gabo was between 20 and 30 mg CO₂ dm^-2 leaf surface hour^-1 under the conditions used. About 45% of flag-leaf assimilates were translocated to the ear, and only about 12% to the roots and young shoots.On removing the ear, net photosynthesis by the flag leaves was reduced by about 50% within 3–15 hours, and there was a marked reduction in the outflow of ¹⁴C-labelled assimilates from the flag leaves.Subsequent darkening of all other leaves on plants without ears led to recovery of flag-leaf photosynthesis, as measured by gas analysis and ¹⁴CO₂ fixation, and to increased translocation of assimilates to the roots and young shoots. Minor changes in the rates of dark respiration accompanied these major, reversible changes in photosynthetic rate.After more than a week in continuous, high-intensity light, the rate of photosynthesis by flag leaves of intact plants had fallen considerably, but could be restored again by a period in darkness, or by inhibiting photosynthesis in the ears by spraying them with DCMU. The inhibition of ear photosynthesis increased translocation of labelled assimilates from the flag leaf to the ears, without affecting leaf sugar levels.The application of TIBA to the culm below the ear inhibited auxin movement throught the culm, but had no influence on flag-leaf photosynthesis.These results suggest that, at least in this system, photosynthesis by the flag leaf is regulated directly by the demand for assimilates from the flag leaf and not indirectly through action in the leaf of auxins produced by the sink organs.     

Effect of salt and soil water status on transpiration of Salsola kali L.

Abstract Transpiration of Salsola kali L. plants, grown in small pots under controlled environmental conditions, was followed through a drying cycle of the soil. Three different nutrient solutions were used during the preconditioning growth period: control (C), half-strength Hoagland's nutrient solution; C plus 150mol m⁻³ NaCl; and C plus 150mol m⁻³ KCl. Soil water content at saturation at the beginning of the drying cycle was 20% (w/w). Both NaCl and KCl treatments modified the plants' response to changes in soil water status. The control plants transpired twice as much (per unit leaf dry weight) as the salt-treated plants, even when the soil was at maximal water capacity. Transpiration of the control plants remained high, until the soil water content declined to 5%. After that stage the stomata of these plants closed abruptly. Transpiration of the salt-treated plants started decreasing when the soil water content was approximately 16%, and did so gradually until all the available water was depleted. When transpiration was plotted against soil water potential a sharp decline in the transpiration of control plants was observed with the soil water potential decreasing from -0.04 to -1.2MPa. Transpiration of the salt-treated plants decreased gradually over a wide range of soil water potential (−0.8 to −7.0MPa).     

Does Rubisco control the rate of photosynthesis and plant growth? An exercise in molecular ecophysiology

Experiments are described in which tobacco (Nicotiana tabacum L.) transformed with antisense rbcS to decrease expression of ribulose-1,5-bisphosphate carboxylase-oxygenase (Rubisco) was used to evaluate the contribution of Rubisco to the control of photosynthetic rate, and the impact of a changed rate of photosynthesis on whole plant composition, allocation and growth. (1) The concept of flux control coefficients is introduced. It is discussed how, with adequate precautions, a set of wild-type and transgenic plants with varying expression of an enzyme can be used to obtain experimental values for its flux control coefficient. (2) The flux control coefficient of Rubisco for photosynthesis depends on the short-term conditions. It increases in high light, or low CO₂. (3) When plants are grown under constant irradiance, the flux control coefficient in the growth conditions is low (<0.2) at irradiances of up to 1000μmol quanta m⁻² s⁻¹. In a natural irradiance regime exceeding 1500μmol quanta m⁻² s⁻² over several hours the flux coefficient rose to 0.8–0.9. It is concluded that plants are able to adjust the balance between Rubisco and the remainder of the photosynthetic machinery, and thereby avoid a one-sided limitation of photosynthesis by Rubisco over a wide range of ambient growth irradiance regimes. (4) When the plants were grown on limiting inorganic nitrogen, Rubisco had a higher flux control coefficient (0.5). It is proposed that, in many growth conditions, part of the investment in Rubisco may be viewed as a nitrogen store, albeit bringing additional marginal advantages with respect to photosynthetic rate and water use efficiency. (5) A change in the rate of photosynthesis did not automatically translate into a change in growth rate. Several factors are identified which contribute to this buffering of growth against a changed photosynthetic rate. (6) There is an alteration in whole plant allocation, resulting in an increase in the leaf area ratio. The increase is mainly due to a higher leaf water content, and not to changes in shoot/root allocation. This increased investment in whole plant leaf area partly counteracts the decreased efficiency of photosynthesis at the biochemical level. (7) Plants with decreased Rubisco have a lower intrinsic water use efficiency and contain high levels of inorganic cations and anions. It is proposed that these are a consequence of the increased rate of transpiration, and that the resulting osmotic potential might be a contributory factor to the increased water content and expansion of the leaves. (8) Starch accumulation in source leaves is decreased when unit leaf photosynthesis is reduced, allowing a more efficient use of the fixed carbon. (9) Decreased availability of carbohydrates leads to a down-regulation of nitrate assimilation, acting via a decrease in nitrate reductase activity.     

Differential inhibition of photosynthesis during pre-flowering drought stress in Sorghum bicolor genotypes with different senescence traits

Young (16-day-old) Sorghum bicolor plants of a late- and slow-senescing Texas A&M line (B 35) and of an early- and fast-senescing descendant of an Ethiopian landrace (E 36-1) were subjected to drought stress by decreasing the soil water content to 30% field capacity over 6 days. Plant water potentials decreased from − 2 bar (controls) to − 10 to − 18 bar, and this drought stress resulted in: (1) differential phenotypic reactions and (2) differential decreases in photosynthesis rates in the two cultivars. While E 36-1 tended to lose viable leaf area from the leaf tips downwards, B 35 showed a gradual overall drying of the leaf. At the same time, photosynthesis rates decreased from 31.5 ± 1.6 to 12.3 ± 5.0 µmol CO₂ m⁻² s⁻¹ (E 36-1) and from 30.5 ± 1.6 to 3.3 ± 2.6 µmol CO₂ m⁻² s⁻¹ (B 35), respectively. In vitro enzyme activities of phosphoenolpyruvate carboxylase (PEPCase), malate dehydrogenase (MDH) and malic enzyme (ME) on a leaf area basis exceeded the photosynthesis rates. Pyruvate phosphate dikinase (PPDK) activity was close to the photosynthesis rates in control plants and higher than the photosynthesis rates in drought-stressed plants. Thus, none of the enzymes appeared to limit photosynthesis under drought stress, and likely bottleneck enzyme activities of the C3 pathway in the bundle-sheath cells, i.e. ribulose-1,5-bisphosphate carboxylase (RubisCO) and stromal fructose-1,5-bisphosphatase (sFBPase), also showed sufficient activities to sustain higher photosynthesis rates than those observed in the stressed plants. However, under drought stress, total leaf malate concentrations were higher in B 35 (up to 33.1 µmol g⁻¹ FW) than in E 36-1 (up to 22.4 µmol g⁻¹ FW). In particular, at the presumed cytosolic pH of 7.0–7.3, S. bicolor PEPCase was strongly inhibited by malate. In contrast with the in vitro PEPCase enzyme activities, the A/C_i curves suggested a stronger decrease in the in vivo activity of the enzyme in B 35 under drought stress than in E 36-1. It is therefore suggested that photosynthesis under drought stress may be inhibited differentially through feedback malate inhibition of PEPCase in S. bicolor.     

Leaf age does not justify its early removal in Carica papaya L

This study evaluated gas exchange and therefore sink/source condition of papaya leaves as they age in order to determine the right moment for leaf blade removal under two different strategies of climate control in greenhouses of Almería (SE Spain): Passive control (PCC; climate control of the greenhouse consisting of natural ventilation by only lateral and roof windows) versus active control (ACC; in addition to the natural ventilation, the greenhouse also incorporated a nebulization and a heating system). The effects of improved climate control were determined on papaya leaves distributed in five different positions in the canopy: S1, S2, S3, S4, S5, where S1 represented the youngest leaf, whereas S5 was the oldest (senescent) leaf present in the plant canopy. We observed that all age leaves presented positive values of net photosynthesis (A_net) despite reduced light availability under plastic greenhouses. In order to separate the effects of limited light availability from the leaf age (position in the canopy), we then repeated gas exchange measurements using artificial light (400 μmol m² s⁻¹) equal for all treatments and observed that the leaves of the ACC increased up to 96% their photosynthetic rates with respect to natural light. ACC plants presented also higher A_net/g_s, showing better intrinsic water use efficiency. Based on these results, we discourage blade removal of papaya leaves when light availability above 400 μmol m² s⁻¹ is assured by correct plant spacing and cultural management.     

Screening a cucumber crop during leaf area development reduces yield

In order to reduce heat energy consumption in greenhouse cucumber production, (transparent) screens may be used also during the day, particularly in the early growth phase when high temperatures are required to achieve rapid leaf area development. However, energy savings must be optimised against light reduction‐induced yield loss. For this reason, two experiments were conducted to quantify the effect on photosynthesis and growth of screening cucumber plants during their early growth phase, and on yield in the following generative phase. Screening with different light transmission coefficients was simulated using shading nets. Shading the plants during the first 5 weeks under Central European winter conditions reduced the leaf area by 0.40% per 1% reduction in photosynthetic active radiation (PAR). Moreover, potential leaf net photosynthesis decreased by 0.46% per 1% PAR reduction. A major impact was that the leaf dry matter content, leaf starch content and leaf sugar content of shaded plants diminished significantly. In the course of the following 2 weeks under full light, the leaf photosynthesis of the plants previously shaded recovered fully and the leaf area index rose to 3.3 m² m^?2, considered sufficient for optimal crop photosynthesis. The yield from plants previously shaded diminished slightly as early as from the first harvest week on. These yield losses increased further over the next few weeks, measuring approximately 0.8 kg m^?2 per 1 mol m^?2 day^?1 PAR reduction in the early growth phase. The effect of PAR on plant growth was proportional when relating the PAR integral over the entire experimental period to the total yield and to the total dry matter production, respectively.     

PHOTOAUTOTROPHIC GROWTH OF A RECENTLY ISOLATED N2-FIXING MARINE NON-HETEROCYSTOUS FILAMENTOUS CYANOBACTERIUM, SYMPLOCA SP. (CYANOBACTERIA)

Photoautotrophic growth of a marine non-heterocystous filamentous cyanobacterium, Symploca sp. strain S84, was examined under nitrate-assimilating and N₂-fixing conditions. Under continuous light, photon flux density of 55 μmol photons·m⁻² ·s⁻¹ was at a saturating level for growth, and light did not inhibit the growth rate under N₂-fixing conditions even when the photon flux density was doubled (110 μmol photons·m⁻² ·s⁻¹). Doubling times of the N₂-fixing cultures under 55 and 110 μmol photons·m⁻² ·s⁻¹ were about 30 and 31 h, respectively. Under 110 μmol photons·m⁻² ·s⁻¹ during the light phase of an alternating 12:12-h light:dark (L:D) cycle, the doubling time of the N₂-fixing culture was also about 30 h. When grown diazotrophically under a 12:12-h L:D regime, C₂H₂ reduction activity was observed mainly during darkness. In continuous light, relatively large cyclic fluctuations in C₂H₂ reduction were observed during growth. The short-term (<4 h) effect of 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU; 5 μM) indicated that C₂H₂ reduction activity was not influenced by photosynthetic O₂ evolution. Long-term (24 h) effects of DCMU indicated that photosynthesis and C₂H₂ reduction activity occur simultaneously. These results indicate that strain S84 grows well under diazotrophic conditions when saturating light is supplied either continuously or under a 12:12-h L:D diel light regime.     

Photosynthetic and stomatal responses of spinach leaves to salt stress

The gas exchange of spinach plants, salt-stressed by adding NaCl to the nutrient solution in increments of 25 millimolar per day to a final concentration of 200 millimolar, was studied 3 weeks after starting NaCl treatment. Photosynthesis became light saturated at 1100 to 1400 micromoles per square meter per second in salt-treated plants and at approximately 2000 micromoles per square meter per second in control plants. Photosynthetic capacity of the mesophyll measured as a function of intercellular partial pressure of CO₂ at the light intensity prevailing during growth and at light saturation were both decreased in the salttreated plants. The CO₂ compensation points and relative enhancements of photosynthesis at low O₂ were not affected by salinity. The lower photosynthetic rates in salt-treated leaves at 450 micromoles per square meter per second were associated with a 70% reduction in stomatal conductance and low intercellular CO₂ (219 microbars; cf. 285 microbars for controls). Increasing photon flux density to light saturation extended the linear portions of the CO₂ response curves, increased stomatal conductances, increased intercellular CO₂ in the salt-treated plants, but lowered it in controls, and accentuated differences in photosynthetic rate (area basis) between the treatments.

Leaves from salt-treated plants were thicker but contained about 73% of the chlorophyll per unit area of control plants. When photosynthetic rates were expressed on a chlorophyll basis there was no difference in initial slope of assimilation versus intercellular CO₂ between treatments. Photosynthetic rates (chlorophyll basis) at light saturation differed only by 20% which was also observed earlier with isolated, intact chloroplasts (Robinson et al. 1983 Plant Physiol 73: 238-242).

Measurement of carbon isotope ratio revealed less discrimination against ¹³C with salt treatment and confirmed the persistence of low intercellular partial pressures of CO₂ during plant growth. The development of a thicker leaf with less chlorophyll per unit area during salt treatment permitted stomatal conductance and intercellular partial pressure of CO₂ to decline without restricting photosynthesis and had the benefit of greatly increasing water use efficiency.

     

Photosynthesis and respiration in bladelets of Ecklonia cava Kjellman (Laminariales, Phaeophyta) in two localities with different temperature conditions

Characteristics of photosynthesis and respiration of bladelets were compared between Ecklonia cava Kjellman sporophytes growing in a warmer temperate locality (Tei, Kochi Pref., southern Japan) and in a cooler temperate locality (Nabeta, Shizuoka Pref., central Japan). Photosynthesis and respiration were measured with a differential gas-volumeter (Productmeter). In photosynthesis-light curves at 20°C, the rate of net photosynthesis was almost the same at light intensities lower than 25 μmol m⁻² s⁻¹ and the light-saturation occurred at 200–400 μmol m⁻²s⁻¹ in plants of both localities. The light-saturated net photosynthetic rates were higher in winter and spring than in summer and autumn in both plants. The optimum temperature for net photosynthesis at 400 μmol m⁻²s⁻¹ was 27°C throughout the year in the Tei plant and 25–27°C in the Nabeta plant. The decrease of net photosynthetic rates in the supraoptimal temperature range up to 29°C was sharper in winter and spring than in summer and autumn in both plants, being smaller in the Tei plant than in the Nabeta plant in all seasons. The dark respiration rate always increased with water temperature rise in both plants. No clear differences were found in the dark respiration rate between Tei and Nabeta plants except that when measured against dry weight, the Tei plant showed a slightly lower rate as compared with the Nabeta plant.     

EFFECTS OF CANOPY POSITION AND IRRADIANCE ON THE LEAF PHYSIOLOGY AND MORPHOLOGY OF PENTACLETHRA MACROLOBA (MIMOSACEAE)

Pentaclethra macroloba (Willd.) Kuntze (Mimosaceae) is a dominant late-successional tree species in the Atlantic lowland forests of Costa Rica. Leaves of P. macroloba from three heights in the forest canopy were compared with leaves of seedlings grown in controlled environment chambers under four different irradiance levels. Changes in leaf characteristics along the canopy gradient paralleled changes resulting from the light gradient under controlled conditions. The effect of light or canopy position on light-saturated photosynthesis was small, with maximum photosynthesis increasing from 5 to 6.5 μmol m^−-2 s^−-1 from understory to canopy. Both chamber grown and field leaves showed large adjustments in photosynthetic efficiency at low light via reductions in dark respiration rates and increases in apparent quantum yields. Light saturation of all leaves occurred at or below 500 μmol m^−-2 s^−-1. Leaf thickness, specific leaf weight, and stomatal density increased to a greater extent than saturated photosynthesis with higher irradiance during growth or height in the canopy. As a result, there was a poor correspondence between leaf thickness and light-saturated photosynthesis on an area basis. It is concluded that Pentaclethra macroloba possesses the characteristics of a typical shade-tolerant species.     

Acclimation of photosynthesis to lightflecks in tomato leaves: interaction with progressive shading in a growing canopy

Plants in natural environments are often exposed to fluctuations in light intensity, and leaf‐level acclimation to light may be affected by those fluctuations. Concurrently, leaves acclimated to a given light climate can become progressively shaded as new leaves emerge and grow above them. Acclimation to shade alters characteristics such as photosynthetic capacity. To investigate the interaction of fluctuating light and progressive shading, we exposed three‐week old tomato (Solanum lycopersicum ) plants to either lightflecks or constant light intensities. Lightflecks of 20 s length and 1000 μmol m^?2 s^?1 peak intensity were applied every 5 min for 16 h per day, for 3 weeks. Lightfleck and constant light treatments received identical daily light sums (15.2 mol m^?2 day^?1). Photosynthesis was monitored in leaves 2 and 4 (counting from the bottom) during canopy development throughout the experiment. Several dynamic and steady‐state characteristics of photosynthesis became enhanced by fluctuating light when leaves were partially shaded by the upper canopy, but much less so when they were fully exposed to lightflecks. This was the case for CO₂‐saturated photosynthesis rates in leaves 2 and 4 growing under lightflecks 14 days into the treatment period. Also, leaf 2 of plants in the lightfleck treatment showed significantly faster rates of photosynthetic induction when exposed to a stepwise change in light intensity on day 15. As the plants grew larger and these leaves became increasingly shaded, acclimation of leaf‐level photosynthesis to lightflecks disappeared. These results highlight continuous acclimation of leaf photosynthesis to changing light conditions inside developing canopies.     

Effects of intraspecific competition on growth and photosynthesis of Atriplex prostrata

We investigated the effect of intraspecific competition on growth parameters and photosynthesis of the salt marsh species Atriplex prostrata Boucher in order to distinguish the effects of density-dependent growth inhibition from salt stress. High plant density caused a reduction of 30% in height, 82% in stem dry mass, 80% in leaf dry mass, and 95% in root dry mass. High density also induced a pronounced 72% reduction in leaf area, 29% decrease in length of mature internodes and 50% decline in net photosynthetic rate. The alteration of net photosynthesis paralleled growth inhibition, decreasing from 7.6 ± 0.9 μmol CO₂ m⁻² s⁻¹ at low density to 3.5 ± 0.4 μmol CO₂ m⁻² s⁻¹ at high density, indicating growth inhibition caused by intraspecific competition is mainly due to a decline in net photosynthesis rate. Plants grown at high density also exhibited a reduction in stomatal conductance from 0.7 ± 0.1 mol H₂O m⁻² s⁻¹ at low density to 0.3 ± 0.1 mol H₂O m⁻² s⁻¹ at high density and a reduction in transpiration rate from 6.0 ± 0.3 mmol H₂O m⁻² s⁻¹ at low density to 4.3 ± 0.3 mmol H₂O m⁻² s⁻¹ at high density. Biomass production was inhibited by an increase in plant density, which reduced the rate of photosynthesis, stomatal conductance and leaf area of plants.     

The influence of light environment on photosynthesis and basal methylbutenol emission from Pinus ponderosa

Methylbutenol is a 5-carbon alcohol that is produced and emitted by several species of pine in western North America, and may have important impacts on the tropospheric chemistry of this region. In the present study the response of methylbutenol basal emission rate (measured at a constant light intensity of 1500 µmol m⁻² s⁻¹ and temperature of 30 °C) to the light and temperature conditions of the growth environment was examined, using field-grown plants shielded with shade cloth of various densities. Methylbutenol basal emission rates increased linearly with the temperature of the growth environment but did not respond to the shading of foliage during growth and development. Both photosynthesis and basal methylbutenol emission rate declined in older needles; however, these declines appear to result from parallel but independent processes and not from basal MBO emission rate directly tracking photosynthetic rates. Older needles did not occupy cooler microenvironments within the canopy; and thus differing thermal microenvironment could not explain the reduced MBO emission in older needles.     

Stomatal development and associated photosynthetic performance of capsicum in response to differential light availabilities

The mechanisms of capsicum growth in response to differential light availabilities are still not well elucidated. Hereby, we analyzed differential light availabilities on the relationship between stomatal characters and leaf growth, as well as photosynthetic performance. We used either 450–500 μmol m⁻² s⁻¹ as high light (HL) or 80–100 μmol m⁻² s⁻¹ as low light (LL) as treatments for two different cultivars. Our results showed that the stomatal density (SD) and stomatal index (SI) increased along with the leaf area expansion until the peak of the correlation curve, and then decreased. SD and SI were lower under the LL condition after three days of leaf expansion. For both cultivars, downregulation of photosynthesis and electron transport components was observed in LL-grown plants as indicated by lower light- and CO₂-saturated photosynthetic rate (P _max and RuBP_max), quantum efficiency of photosystem II (PSII) photochemistry (Φ_PSII), electron transport rate (ETR) and photochemical quenching of fluorescence (q_p). The observed inhibition of the photosynthesis could be explained by the decrease of SD, SI, Rubisco content and by the changes of the chloroplast. The low light resulted in lower total biomass, root/shoot ratio, and the thickness of the leaf decreased. However, the specific leaf area (SLA) and the content of leaf pigments were higher in LL-treatment. Variations in the photosynthetic characteristics of capsicum grown under different light conditions reflected the physiological adaptations to the changing light environments.     

Changing Sink Demand Affects the Area but not the Specific Activity of Assimilate Sources in Cantaloupe (Cucumis meloL.)

To better understand source-sink interactions, this work focusedon the influence of fruit number on leaf area and photosyntheticactivity in cantaloupe. To this end, flowers were removed over2 years on two Charentais cultivars to obtain single-fruit plantsand plants with an unrestricted fruit load (which set two tofive fruits and constituted control plants). At the whole plantscale, net photosynthesis was reduced by about 30% under highfruit load. At the leaf scale, a submodel of stomatal conductancewas fitted to the data and was included in a rectangular hyperbolamodel of leaf photosynthesis. Maximum leaf net photosynthesisaveraged 14.83 µmol CO₂m^-2s^-1at 1000 µmol quantam^-2s^-1. Light use efficiency was not affected by fruit loadand equalled 0.040 mol CO₂mol^-1quanta. Leaf area of plants withunrestricted fruit load decreased after 24 days from pollination,while the leaf area of single-fruit plants was still increasing.The decrease was due to production of fewer new leaves per day,whereas the number of senescent leaves and the size of individualleaves were not affected by the treatment. Under high fruitload, cultivar Galoubet developed a larger projected leaf areathan cultivar Talma. Thus it is concluded that: (1) large cantaloupefruits may divert a large amount of assimilates away from, andgrow at the expense of, the canopy; and (2) photosynthesis ofthe canopy was lowered because leaf area was reduced whereasphotosynthetic rate of leaves was not altered.Copyright 1998Annals of Botany Company. Cucumis meloL., fruit load, source-sink interactions, leaf photosynthesis, canopy photosynthesis, leaf area, SLA, source strength.     

Steady-state stomatal responses of C3 and C4 species to blue light fraction: Interactions with CO2 concentration

Blue light induced stomatal opening has been studied by applying a short pulse (~5 to 60 s) of blue light to a background of saturating photosynthetic red photons, but little is known about steady-state stomatal responses. Here we report stomatal responses to blue light at high and low CO₂ concentrations. Steady-state stomatal conductance (g_s) of C₃ plants increased asymptotically with increasing blue light to a maximum at 20% blue (120 μmol m⁻² s⁻¹). This response was consistent from 200 to 800 μmol mol⁻¹ atmospheric CO₂ (C_a). In contrast, blue light induced only a transient stomatal opening (~5 min) in C₄ species above a C_a of 400 μmol mol⁻¹. Steady-state g_s of C₄ plants generally decreased with increasing blue intensity. The net photosynthetic rate of all species decreased above 20% blue because blue photons have lower quantum yield (moles carbon fixed per mole photons absorbed) than red photons. Our findings indicate that photosynthesis, rather than a blue light signal, plays a dominant role in stomatal regulation in C₄ species. Additionally, we found that blue light affected only stomata on the illuminated side of the leaf. Contrary to widely held belief, the blue light-induced stomatal opening minimally enhanced photosynthesis and consistently decreased water use efficiency.     

Two Steps of Gas Exchange in Leaf Photosynthesis

Photosynthesis and transpiration of excised leaves of Taraxacum officinale L. and a few other species of plants were measured, using an open gas analysis system. The rates of CO₂ uptake and transpiration increased in two steps upon illumination of stomata-bearing epidermis of these leaves at a light intensity of 50 mW × cm⁻². Abscisic acid inhibited only the second step of gas exchange. Illumination of the astomatous epidermis of hypostomatous leaves caused only the first step of gas exchange. These data indicate that the first and second steps arise from cuticular and stomatal gas exchange, respectively. The rate of the cuticular photosynthesis in a Taraxacum leaf reached saturation at a light intensity of 5 mW × cm⁻², and the rates of the stomatal photosynthesis and transpiration reached saturation at a higher intensity of 35 mW × cm⁻². The cuticular photosynthesis of a Taraxacum leaf was 18% of the stomatal photosynthesis at 50 mW × cm⁻² and 270% at 5 mW × cm⁻². The other species of leaves showed the same trend. The importance of cuticular CO₂ uptake in leaf photosynthesis, especially under low light intensity was stressed from these data.     

Microgravity does not alter plant stand gas exchange of wheat at moderate light levels and saturating CO<Subscript>2</Subscript> concentration

Plant stand gas exchange was measured nondestructively in microgravity during the Photosynthesis Experiment Subsystem Testing and Operations experiment conducted onboard the International Space Station. Rates of evapotranspiration and photosynthesis measured in space were compared with ground controls to determine if microgravity directly affects whole-stand gas exchange of Triticum aestivum. During six 21-day experiment cycles, evapotranspiration was determined continuously from water addition rates to the nutrient delivery system, and photosynthesis was determined from the amount of CO₂ added to maintain the chamber CO₂ concentration setpoint. Plant stand evapotranspiration, net photosynthesis, and water use efficiency were not altered by microgravity. Although leaf area was significantly reduced in microgravity-grown plants compared to ground control plants, leaf area distribution was not affected enough to cause significant differences in the amounts of light absorbed by the flight and ground control plant stands. Microgravity also did not affect the response of evapotranspiration to changes in chamber vapor pressure difference of 12-day-old wheat plant stands. These results suggest that gravity naïve plants grown at moderate light levels (300 mol m^–2 s^–1) behave the same as ground control plants. This implies that future plant-based regenerative life support systems can be sized using 1 g data because water purification and food production rates operate at nearly the same rates as in 1 g at moderate light levels. However, it remains to be verified whether the present results are reproducible in plants grown under stronger light levels.