Effects of Sulphur Dioxide and Nitrogen Dioxide on Growth and Translocation in Winter Wheat

Gould, R. P. and Mansfield, T. A. 1988. Effects of sulphur dioxideand nitrogen dioxide on growth and translocation in winter wheat.—J. exp. Bot 39: 389–99 Winter wheat (Triticum aestivum L. cv. Avalon) was grown undersimulated autumn conditions for 4 weeks and exposed to a mixtureof SO₂ and NO₂. Biomass was measured after 2, 3 and 4 weeksand the flag leaves of sample plants were labelled with ¹⁴CO₂.Biomass yields revealed an increase in shoot-to-root ratiosunder polluted conditions. The labelling experiments showedthat less assimilate was transported to the roots, whilst morewas allocated to the younger components of the plant. It appearedthat NO₂ and SO₂ also caused labelled photosynthate to be retainedin the labelled leaf. Reducing the photon flux exacerbated theeffects of SO₂ and NO₂ as indicated by changes in biomass andby the distribution of ¹⁴C. Key words: Wheat, SO₂, NO₂, growth, translocation     

The Effects of Sulphur Dioxide on Phloem Transport in Two Cereals

Gould, R. P., Minchin, P. E. H. and Young, P. C. 1988. The effectsof sulphur dioxide on phloem transport in two cereals.—J.exp. BoL 39: 997–1007. In vivo investigations using ¹¹C-labelled photosynthate revealedthat there is a change in the patterns of tracer profiles whencereal leaves are exposed to SO₂. The change after exposureto SO₂ was interpreted in terms of a decrease in lateral waterflow into the sieve tubes brought about by reduced phloem loadingalong the length of a leaf. Analysis also revealed that thespeed of translocation was reduced, as expected by the Munchmodel of phloem transport. Key words: Sulphur dioxide, phloem transport, cereal leaves     

Effect of Light Intensity, Carbon Dioxide Concentration, and Leaf Temperature on Gas Exchange of Spray Carnation Plants

The rates of CO₂ assimilation by potted spray carnation plants(cv. Cerise Royalette) were determined over a wide range oflight intensities (45–450 W m^–2 PAR), CO₂ concentrations(200–3100 vpm), and leaf temperatures (5–35 °C).Assimilation rates varied with these factors in a way similarto the response of single leaves of other temperate crops, althoughthe absolute values were lower. The optimal temperature forCO₂ assimilation was between 5 and 10 °C at 45 W m^–2PAR but it increased progressively with increasing light intensityand CO₂ concentration up to 27 °C at 450 W m^–2 PARand 3100 vpm CO₂ as expressed by the equation TOpt = –6.47-h 2.336 In G + 0.031951 where C is CO₂ concentration in vpmand I is photo-synthetically active radiation in W m^–2.CO₂ enrichment also increased stomatal resistance, especiallyat high light intensities. The influence of these results on optimalization of temperaturesand CO₂ concentrations for carnation crops subjected to dailylight variation, and the discrepancy between optimal temperaturesfor growth and net photosynthesis, are discussed briefly     

Gas Exchange and Flowering in Verticillium-wilted Pepper Plants

In Navarra, Northern Spain, Verticillium dahliae Kleb. is one of the pathogens that causes drastic reductions in pepper production. The aim of this study therefore was to describe how infection by V. dahliae affects gas exchange during the flowering of pepper in order to determine some possible factors contributing to the significant decrease of plant yield. Verticillium was inoculated when plants had started flowering. The first leaf wilting symptoms appeared on day 18 after inoculation, but leaf water potential rapidly decreased after infection. The inoculated plants produced more flowers than the controls between 15 and 33 days after inoculation, but flower production declined after day 33. Inoculated plants also suffered more defoliation and chlorophyll degradation. Leaf conductance and photosynthesis clearly decreased in both groups of plants as a consequence of senescence, but the values in those inoculated were significantly lower. Results suggest that the decrease in photosynthesis was in part due to defoliation and chlorophyll degradation, as well as premature flower fall. These factors contributed to the negative effects of Verticillium infection on pepper yield.     

Autonomous System for Measuring Water Consumption in Plants

An autonomous system based on a constant heating method and designed for measuring water consumption in plants is described. The system was built into an industrially produced potentiometric recorder; it contained two input channels and operated with thermoelectric temperature sensors. The system operation was tested in experiments on mature trees of pedunculate oak (Quercus robur L.).     

Effects of Sulphur Dioxide on Sugar and Free Amino Acid Content of Pine Seedlings

Treatment of jack pine (Pinus banksiana Lamb.) seedlings with gaseous SO₂ resulted in a shift between the reducing and non-reducing sugars. Increasing concentrations of gaseous SO₂ caused an increase in reducing sugars and a decline in the non-reducing sugars, suggesting a conversion from the latter to the former at high SO₂ concentrations. The total amino acid content of the intact tissues also increased with increasing concentrations of gaseous SO₂. Gas-liquid chromatographic analyses of the amino acids indicated that SO₂ (1. 34 mg · m^-3 for 96 h) resulted in an increase in the content of alanine, valine, glycine, isoleucine, leucine, threonine, aspartic acid tyrosine, lysine, and arginine, and a decrease in the content of serine and glutamic acid. The enzymatic and other implications of such changes are discussed.     

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     

Effects of Nitrogen Deficiency on Gas Exchange,Chlorophyll Fluorescence,and Antioxidant Enzymes in Leaves of Rice Plants

Gas exchange, chlorophyll (Chl) fluorescence, and contents of photosynthetic pigments, soluble proteins (ribulose-1,5-bisphosphate carboxylase/oxygenase, RuBPCO), and antioxidant enzymes were characterized in the fully expanded 6^th leaves in rice seedlings grown on either complete (CK) or on nitrogen-deficient nutrient (N-deficiency) solutions during a 20-chase period. Compared with the control plants, the lower photosynthetic capacity at saturation irradiance (P_max) was accompanied by an increase in intercellular CO₂ concentration (C_i), indicating that in N-deficient plants the decline in P_max was not due to stomatal limitation but due to the reduced carboxylation efficiency. The fluorescence parameters _PS2, F_v/F_m, electron transport rate (ETR), and q_P showed the same tendency as P_max in N-deficient plants. Correspondingly, a higher q_N paralleled the rise of the ratio of carotenoid (Car) to Chl contents. However, F_v/F_m was still diminished, suggesting that photoinhibition did occur in the photosystem 2 (PS2) reaction centres. In addition, the activities of antioxidant enzymes on a fresh mass basis were gradually lowered, leading to the aggravation of membrane lipid peroxidation with the proceeding N-deficiency. The accumulation of malonyldialdehyde resulted in the lessening of Chl and soluble protein content. Analyses of regression showed PS2 excitation pressure (1 - q_P) was linearly correlated with the content of Chl and inversely with soluble protein (particularly RuBPCO) content. There was a lag phase in the increase of PS2 excitation pressure compared to the decrease of RuBPCO content. Therefore, the increased excitation pressure under N-deficiency is probably the result of saturation of the electron transport chain due to the limitation of the use of reductants by the Calvin cycle. Rice plants responded to N-deficiency and high irradiance by decreasing light-harvesting capacity and by increasing thermal dissipation of absorbed energy.     

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.     

Gas Exchange of In Vitro and Ex Vitro Grown Grapevine Plants

Net photosynthetic rate (P _N) and dark respiration rate (R _D) were measured in Vitis vinifera L. cvs. Dimiat 4/24 (23^rd subculture), Dimiat 4/38 (22^nd subculture), and Italian Riesling 3/47 (22^nd subculture) on days 3, 2, and 1 (1^st series) before transfer from the in vitro culture and on days 14, 15, 16 (2^nd series) and 28, 29, 30 (3^rd series) after the transfer. P _N of in vitro and ex vitro plants was strongly affected by irradiance. P _N and R _D of in vitro plantlets were lower and transpiration rate (E) was higher compared to those of ex vitro plantlets. P _N, R _D, and E changed in the course of acclimation.     

Simultaneous Measurement of Oxygen, Carbon Dioxide, and Water Vapour Exchange in Intact Plants

A low flow of air is passed through a temperature-controlledplant chamber in order to obtain relatively large (300–500µl-1) differences in [O₂] between influx and efflux streams.These differences are measured with a stabilized O₂ electrodesystem incorporating elements of gas conditioning electroniczero suppression and signal amplification. Changes in [O₂] of400 µl l-1 can be detected at full scale recorder deflectionagainst a background concentration of 21% O₂. The concentrationsof CO₂ and H₂O within the chamber are held constant by con-trolled-flowCO₂-scrubbing and dehumidifying loops. Carbon dioxide, H₂O,and O₂ fluxes are measured and leaf diffusion resistance andinternal [CO₂] are calculated in essentially ‘real time’.     

A Rapid Field Method for Measuring Photosynthesis with Labelled Carbon Dioxide

A portable field apparatus for the measurement of photosynthesisis described. Short pulses (20 s) of air containing ¹⁴CO₂ areapplied to circular leaf areas of 1 cm², enclosed in a transparentminiature chamber; the radioactivity of the leaf areas is measuredby liquid scintillation, using a new in-vial wet combustiontechnique. Typical daily courses of photosynthesis in maizeand cotton are presented.     

A System for Measuring the Uptake of Ions by Plants from Flowing Solutions of Controlled Composition

A system is described for growing plants in flowing solutionin which the concentration (activity) of some nutrient ionsis continuously monitored and held almost constant by meansof ion-selective electrodes which control the operation of nutrientpumps. By recording the concentration of a given ion in theflowing nutrient solution and the amount of that ion which isdelivered by the nutrient pumps, it is possible to follow nutrientuptake over long and short periods. A brief account is givenof the operation of the system using a nitrate ion-selectiveelectrode to examine aspects of uptake by perennial ryegrass (Lolium perenne L.).     

Interactive Effects of Sulphur Dioxide and Mineral Nutrient Supply on Photosynthetic Characteristics and Yield in Four Wheat Cultivars

Field experiments were conducted on four cultivars of wheat (Triticum aestivum L.) to examine the variability in cultivar response to sulphur dioxide (SO₂) under different concentrations of mineral nutrients. Thirty-days-old plants were exposed for 8 weeks to 390±20 µg m^–3 (0.15 ppm) SO₂ for 4 h per day, 5 d per week. Decline in net photosynthetic rate, contents of pigments and nitrogen, biomass and grain yield of each cultivars were due to SO₂ at all the nutrient concentrations studied. However, the magnitude of reduction was higher in plants grown without nutrient application. On the basis of the reductions in photosynthesis and yield, the susceptibility of wheat cultivars to SO₂ was in the order of Malviya 213 > Malviya 37 > Malviya 206 > Malviya 234 at recommended dose of NPK, whereas the same without the nutrients was Malviya 206 > Malviya 234 > Malviya 213 > Malviya 37.     

Effects of Irradiance-Sulphur Interactions on Enzymes of Carbon,Nitrogen, and Sulphur Metabolism in Maize Plants

The effect of sulphur deprivation and irradiance (180 and 750 µmol m^–2 s^–1) on plant growth and enzyme activities of carbon, nitrogen, and sulphur metabolism were studied in maize (Zea mays L. Pioneer cv. Latina) plants over a 15-d-period of growth. Increase in irradiance resulted in an enhancement of several enzyme activities and generally accelerated the development of S deficiency. ATP sulphurylase (ATPs; EC 2.7.7.4) and o-acetylserine sulphydrylase (OASs; EC 4.2.99.8) showed a particular and different pattern as both enzymes exhibited maximum activity after 10 d from the beginning of deprivation period. Hence in maize leaves the enzymes of C, N, and S metabolism were differently regulated during the leaf development by irradiance and sulphur starvation.     

Response of Bean (Vicia faba L.) Plants to Low Sink Demand by Measuring the Gas Exchange Rates and Chlorophyll a Fluorescence Kinetics

Background

The decline of photosynthesis in plants under low sink demand is well known. Previous studies focused on the relationship between stomatal conductance (g _s) and net photosynthetic rate (P _n). These studies investigated the effect of changes in Photosystem II (PSII) function on the P _n decline under low sink demand. However, little is known about its effects on different limiting steps of electron transport chain in PSII under this condition.

Methodology/Principal Finding

Two-month-old bean plants were processed by removing pods and flowers (low sink demand). On the 1^st day after low sink demand treatment, a decline of P _n was accompanied by a decrease in g _s and internal-to-ambient CO₂ concentration ratio (C _i/C _a). From the 3^rd to 9^th day, P _n and g _s declined continuously while C _i/C _a ratio remained stable in the treatment. Moreover, these values were lower than that of control. W_k (a parameter reflecting the damage to oxygen evolving complex of the donor side of PSII) values in the treatment were significantly higher than their corresponding control values. However, RC_QA (a parameter reflecting the number of active RCs per excited cross-section of PSII) values in the treatment were significantly lower than control from the 5^th day. From the 11^th to 21^st day, P _n and g _s of the treatment continued to decline and were lower than control. This was accompanied by a decrease of RC_QA, and an increase of W_k. Furthermore, the quantum yield parameters φ _Po, φ _Eo and ψ _Eo in the treatment were lower than in control; however, C _i/C _a values in the treatment gradually increased and were significantly higher than control on the 21^st day.

Conclusions

Stomatal limitation during the early stage, whereas a combination of stomatal and non-stomatal limitation during the middle stage might be responsible for the reduction of P _n under low sink demand. Non-stomatal limitation during the late stages after the removal of the sink of roots and pods may also cause P _n reduction. The non-stomatal limitation was associated with the inhibition of PSII electron transport chain. Our data suggests that the donor side of PSII was the most sensitive to low sink demand followed by the reaction center of PSII. The acceptor side of PSII may be the least sensitive.