Photosynthetic efficiency during ontogenesis of leaves of Betula pendula

Abstract. Net photosynthesis, photosynthetic electron transport, and leaf area density of photosynthetic units have been studied in developing, mature, and old leaves of seedlings of Betula pendula . The photosynthetic quantum yield under light-limiting conditions and the leaf area related rale of light-saturated net photosynthesis were lower in developing than in mature and old leaves. Developing leaves also had more oxygen inhibition of photosynthesis, a lower pool size of plastoquinone in the electron transport chain, a lower chlorophyll content and a lower leaf area density of photosynthetic units than mature and old leaves. The photosynthetic properties of The oldest leaves resulted partly from acclimation to shade and partly from a different ontogeny to that of younger leaves.     

Photosynthetic properties of leaves of Eupatorium makinoi infected by a geminivirus

We examined photosynthetic properties of Eupatorium makinoi leaves infected by a geminivirus. Since a major symptom of the geminivirus infection is variegation or yellowing of leaves, Chl content was used as an index of disease severity. As leaf Chl content was lowered, leaf absorptance, maximal quantum yield of photosynthesis on an absorbed quantum basis (o_2,max) and light-saturated rate of photosynthesis (P_max) decreased. The share of energy allocated to PS II, which can be estimated from fluorescence parameters and oxygen evolution rate, was about 30% lower in the infected yellow leaves than in uninfected leaves. Analyses of the composition of thylakoid polypeptides by gel electrophoresis showed preferential loss of LHC II. The lower o_2,maxin the infected leaves was, thus, attributed to the decreased energy allocation to PS II. These features were largely consistent with those of b-less mutants, but lowered P_maxhas been never reported for b-less mutants. Possible mechanisms causing these changes in photosynthetic properties to the infected leaves are discussed.     

Measurement of chlorophyll fluorescence within leaves using a modified PAM Fluorometer with a fiber-optic microprobe

By using a fiber-optic microprobe in combination with a modified PAM Fluorometer, chlorophyll fluorescence yield was measured within leaves with spatial resolution of approximately 20 m. The new system employs a miniature photomultiplier for detection of the pulse-modulated fluorescence signal received by the 20 m fiber tip. The obtained signal/noise ratio qualifies for recordings of fluorescence induction kinetics (Kautsky effect), fluorescence quenching by the saturation pulse method and determination of quantum yield of energy conversion at Photosystem II at different sites within a leaf. Examples of the system performance and of practical applications are given. It is demonstrated that the fluorescence rise kinetics are distinctly faster when chloroplasts within the spongy mesophyll are illuminated as compared to palisade chloroplasts. Photoinhibition is shown to affect primarily the quantum yield of the palisade chloroplasts when excessive illumination is applied from the adaxial leaf side. The new system is envisaged to be used in combination with light measurements within leaves for an assessment of the specific contributions of different leaf regions to overall photosynthetic activity and for an integrative modelling of leaf photosynthesis.This paper is dedicated to Ulrich Heber on the occasion of his 65th birthday, with great respect for his outstanding achievements in photosynthesis research.     

Photosynthetic efficiency of Betula pendula acclimated to different quantum flux densities

Abstract. Seedlings of Betula pendula were grown in a controlled environment chamber at quantum flux densities of 50, 250 and 600 μmol m⁻² s⁻¹. The relationship between the flux densities of absorbed CC₂ and quanta was determined for shoots of whole seedlings. Rates of both light-saturated and in situ (measured under the growing conditions) net photosynthesis were determined and the pholosynthetic quantum yields under light-limiting conditions were calculated. Anatomical leaf characteristics, chlorophyll contents and sizes and densities of the photosynthetic units (chlorophyll/P700) were determined. Chloroplasts were isolated and their rates of 2,6-dichlorophenol indophenol photoreduction were measured together with their pool sizes of the electron transport carriers plastoquinone and cylochrome ƒ.
Although acclimated to different quantum flux densities, the three birch populations showed the same quantum yield of net photosynthesis. This was approximately 0.028 in normal air (21.2 kPa oxygen) and about 0.040 when photorespiration was largely inhibited in 2.0 kPa oxygen. In addition, the in situ net photosynthesis rates were limited by the absorbed quantum flux density for low, intermediate and high light grown seedlings. It was concluded that birch acclimated to the three light regimes at different levels of organization (metabolic and anatomical). Thus, the quanta which were absorbed in situ could be transferred into chemical equivalents at an optimal and constant efficiency. The use of different reference bases for expressing rates of net photosynthesis are also discussed.     

Photosynthetic activity of far-red light in green plants

We have found that long-wavelength quanta up to 780 nm support oxygen evolution from the leaves of sunflower and bean. The far-red light excitations are supporting the photochemical activity of photosystem II, as is indicated by the increased chlorophyll fluorescence in response to the reduction of the photosystem II primary electron acceptor, Q_A. The results also demonstrate that the far-red photosystem II excitations are susceptible to non-photochemical quenching, although less than the red excitations. Uphill activation energies of 9.8 ± 0.5 kJ mol⁻¹ and 12.5 ± 0.7 kJ mol⁻¹ have been revealed in sunflower leaves for the 716 and 740 nm illumination, respectively, from the temperature dependencies of quantum yields, comparable to the corresponding energy gaps of 8.8 and 14.3 kJ mol⁻¹ between the 716 and 680 nm, and the 740 and 680 nm light quanta. Similarly, the non-photochemical quenching of far-red excitations is facilitated by temperature confirming thermal activation of the far-red quanta to the photosystem II core. The observations are discussed in terms of as yet undisclosed far-red forms of chlorophyll in the photosystem II antenna, reversed (uphill) spill-over of excitation from photosystem I antenna to the photosystem II antenna, as well as absorption from thermally populated vibrational sub-levels of photosystem II chlorophylls in the ground electronic state. From these three interpretations, our analysis favours the first one, i.e., the presence in intact plant leaves of a small number of far-red chlorophylls of photosystem II. Based on analogy with the well-known far-red spectral forms in photosystem I, it is likely that some kind of strongly coupled chlorophyll dimers/aggregates are involved. The similarity of the result for sunflower and bean proves that both the extreme long-wavelength oxygen evolution and the local quantum yield maximum are general properties of the plants.     

Changes in net photosynthetic rate and chlorophyll fluorescence in potato leaves induced by water stress

Net rates of photosynthesis (PN) saturated by irradiance of >500 mol m-2 s-1 (PAR) significantly decreased in water-stressed potato (Solanum tuberosum L. cv. Kufri Sindhuri) plants. The quantum yield of photochemical energy conversion (Fv/Fm), relative electron transport rate (ETR), and photochemical quenching (Qp) exhibited a parallel decline at high irradiance. A slight decrease in relative water content (RWC) was accompanied by a drastic decline in leaf water potential (w) from -0.2 to -1.0 MPa. Dehydrated leaves showed an increase in the amount of total soluble sugars per unit leaf area which inhibited the photosynthesis in a feedback manner. After rewatering, PN and Fv/Fm were restored to the values of control plants within 24 h, and the restoration was accompanied by a proportionate lowering of content of total soluble sugars in the leaves.     

Contrasting modes of regulation of PS II light utilization with changing irradiance in normal and psbS mutant leaves of Arabidopsis thaliana

Complementary techniques of chlorophyll a fluorescence, steady state CO₂ exchange, and O₂ release during a multiple turnover flash were applied to compare responses to irradiance for leaves of wild type and psbS mutants. The latter included variants in which the psbS gene was deleted (npq4-1) or possessed a single point mutation (npq4-9). Nonphotochemical quenching (NPQ) was reduced by up to 80 and 50%, respectively, in these lines at high irradiance. Analysis of changes in steady-state fluorescence yields and quantum yield of linear electron transport in the context of the reversible radical pair model of Photosystem II (PS II) indicated that NPQ occurs by nonradiative deactivation of chlorophyll singlet states in normal leaves. In contrast, application of the same criteria together with the observed irreversibility of NPQ and decline in density of functional PS II reaction centers following excessive illumination indicated a change in reaction center properties for the psbS deletion phenotype (Npq4-1^–). Specifically, PS II reaction centers in Npq4-1^– convert to a photochemically inactive, yet strongly quenching, form in intense light. The possibility of formation of a carotenoid or chlorophyll cation quencher in the reaction center is discussed. Results for the point mutant phenotype (Npq4-9^–) were intermediate to those of wild-type and Npq4-1^–. Furthermore, wild-type leaves exhibited a significant reversible increase in the PS II in vivo rate constant for photochemistry (k_P0) in saturating compared to limiting light. Changes in k_P0 could not be accounted for in terms of a classic phosphorylation-dependent (state transition) mechanism. Changes in k_P0 may arise from alternate pigment—protein conformations that alter the way excitons equilibrate among PS II chromophores. The lack of similar irradiance-dependent changes in k_P0 for the psbS mutants suggests a role for the PS II-S protein in the regulation of exciton distribution.This revised version was published online in October 2005 with corrections to the Cover Date.     

Electron transport and chloroplast ultrastructure of a chlorophyll deficient mutant of wheat

A non-lethal chlorophyll deficient mutation was induced by use of the chemical mutagen ethyl methanesulfonate. Chloroplasts from the control and mutant plants were found to be very similar ultrastructurally. Thylakoid membrane volume was only slightly greater in plastids from the control as compared with plastids from the mutant. The chlorophyll content of the mutant was reduced by over 60%. This decrease in chlorophyll was not accompanied by a similar decrease in electron transport. Uncoupled electron transport rate based on a unit chlorophyll basis was nearly twice as great for mutant chloroplasts as for control plastids. However, electron transport rate based on a unit membrane volume was similar in mutant and control plants. At high irradiance the relative quantum requirement of the control and mutant was similar when expressed on membrane volume.     

Solvent effect on the relative quantum yield and fluorescence quenching of a newly synthesized coumarin derivative

We estimated the relative florescence quantum yield (Φ) of 8‐methoxy‐3‐[1‐(4,5‐dicarbomethoxy‐1,2,3‐triazoloacetyl)]coumarin [8MDTC] using a single‐point method with quinine sulfate in 0.1 M of sulfuric acid used as a standard reference. The fluorescence lifetimes, radiative and non‐radiative decay rate constants are calculated. Relative quantum yields were found to be less in the non‐polar solvents, indicating that the solute exhibits less fluorescence in a non‐polar environment. The fluorescence quenching of [8MDTC] by aniline was studied at room temperature by examining the steady state in five different solvents in order to explore various possible quenching mechanisms. The experimental results show a positive deviation in Stern–Volmer plots in all solvents. Ground state complex and sphere of action static quenching models were used to interpret the results. Many quenching rate parameters were calculated using these models. The values of these parameters suggest that the sphere of action static quenching model agrees well with the experimental results. Further, a finite sink approximation model was used to check whether these bimolecular reactions were diffusion limited or not. The values of the distance parameter R′ and the diffusion coefficient D were determined and are compared with the values of the encounter distance R and diffusion coefficient D calculated using the Stokes–Einstein equation. Copyright © 2014 John Wiley & Sons, Ltd.     

Performance and Photosynthetic Ecophysiology of Three Photo-Types of Dioscorea zingiberensis under Differing Light Intensities

Abstract: The performance and photosynthetic ecophysiology of three photo-types of Dioscorea zingiberensis were studied. The three types are designated DzTL, DzTM and DzTH, according to their adaptation to low (LL), medium (ML) and high (HL) light intensities, respectively. Under LL (23 - 55 μmol m^-2 s^-1) and simulated natural light (SNL), DzTM grows well with increased longevity, and green leaves which are unspotted; while its leaves became small, light yellow and short-lived under HL (550 - 850 μmol m^-2 s^-1). In contrast, under LL the leaves of DzTH were very large, spotted, light yellow and short-lived; while they were small, green and long-lived under HL. Under HL, DzTH had a much higher chlorophyll content than DzTM. Under LL, DzTM and DzTL had a higher Chl content than DzTH. Among the three types, DzTM had the highest peroxidase activity. DzTL had a higher electron transport rate (ETR), maximal quantum yield (MQY) and effective quantum yield (EQY) than DzTH and DzTL under LL, while DzTH had higher ETR, MQY and EQY than the other two types under ML and HL. Therefore, three different photo-types can be characterized according to their adaptation to LL, ML and HL: DzTL, DzTM and DzTH, respectively.     

<Emphasis Type="Italic">PsbS</Emphasis> genotype in relation to coordinated function of PS II and PS I in <Emphasis Type="Italic">Arabidopsis</Emphasis> leaves

Application of multiple probes to systems that carry specific mutations provides a powerful means for studying how known regulators of light utilization interact in vivo. Two lines of Arabidopsis thaliana were studied, each carrying a unique lesion in the nuclear psbS gene encoding a 22-kDa pigment-binding protein (PS II-S) essential for full expression of photoprotective, rapid-phase, nonphotochemical quenching of chlorophyll fluorescence (NPQ). The PS II-S protein is absent in line npq4-1 due to deletion of psbS. Line npq4-9 expresses normal levels of PS II-S but carries a single amino acid substitution that lowers NPQ capacity by about 50%. A prior report [Peterson RB and Havir EA (2001) Planta 214: 142–152] described an altered pattern of redox states of the acceptor side of Photosystem II (PS II) and donor side of Photosystem I (PS I) for npq4-9 suggesting that interphotosystem electron transport may be restricted by a higher transthylakoid ΔpH in this line. In vivo steady state fluorescence and absorbance measurements (820 nm) confirmed these earlier observations for line npq4-9 but not for npq4-1. Thus, the prior results cannot be correlated simply to a loss of NPQ capacity. Likewise, the kinetics of the 820-nm absorbance change did not indicate a substantial effect of psbS genotype on electron flow from plastoquinol to PS I. A simple model is proposed to relate linear electron transport rate (measured gasometrically) to a parameter (based on fluorescence) that provides a relative measure of the density of excitation available for photochemistry in PS II. Surprisingly, analyses using this model suggested that the in vivo midpoint potential of the primary quinone acceptor in PS II (Q_A) is lowered in both psbS mutant lines. This heretofore-unsuspected role for PS II-S is discussed with regard to: (1) numerous prior reports indicating plasticity of the redox potential of Q_A and (2) the basis for the contrasting regulation of quantum yields of PS I and II in npq4-1 and npq4-9.     

Anthocyanin accumulation in the illuminated surface of maize leaves enhances protection from photo-inhibitory risks at low temperature, without further limitation to photosynthesis

At suboptimal temperatures, anthocyanins accumulate in the illuminated leaf surface of some maize genotypes and, if the anthocyanins shade chloroplasts, they can effectively reduce the risk of photo‐inhibition but also photo‐synthesis. To investigate this phenomenon, gas exchange, fluorescence, superoxide dismutase activity and xantho‐phyll composition of anthocyanin‐containing HOPI and anthocyanin‐deficient W22 maize genotypes were measured in either white or red light, where the latter is not absorbed by anthocyanins. Despite differences in light absorption in chloroplasts, photosynthesis did not differ between HOPI and W22 under either light source, suggesting that neither CO₂ supply nor photochemistry were more limiting in red leaves than in green leaves. In fact, no major differences in transpiration were detected. The ΔF/F_m (photosystem II quantum yield) of HOPI in white light was higher than in red light and higher than ΔF/F_m of W22 with either light source. This probably compensated for the lower white light absorption of HOPI chloroplasts compared with W22 because of the presence of anthocyanins and led to similar rates of calculated electron transport for both genotypes. After exposure to high white light at 5 °C, xanthophyll de‐epoxidation and superoxide dismutase activity were lower in HOPI than in W22. Further, HOPI could be exposed to a much higher irradiance than W22 before F_v/F_m was reduced to that of W22.     

Photorespiration is Essential for the Protection of the Photosynthetic Apparatus of C3 Plants Against Photoinactivation Under Sunlight

CO₂ assimilation, transpiration and modulated chlorophyll fluorescence of leaves of Chenopodium bonus-henricus (L.) were measured in the laboratory and, at a high altitude location, in the field. Direct calibration of chlorophyll fluorescence parameters against carbon assimilation in the presence of 1 or 0.5% oxygen (plus CO₂) proved necessary to calculate electron transport under photorespiratory conditions in individual experiments. Even when stomata were open in the field, total electron transport was two to three times higher in sunlight than indicated by net carbon gain. It decreased when stomata were blocked by submerging leaves under water or by forcing them to close in air by cutting the petiole. Even under these conditions, electron transport behind closed stomata approached 10 nmol electrons m^?2 leaf area s^?1 at temperatures between 25 and 30 °C. No photoinactivation of photosystem II was indicated by fluorescence analysis after a day's exposure to full sunlight. Only when leaves were submerged in ice was appreciable photoinactivation noticeable after 4 h exposure to sunlight. Even then almost full recovery occurred overnight. Electron transport behind blocked stomata was much decreased when leaves were darkened for 70 min (in order to deactivate light-regulated enzymes of the Calvin cycle) before exposure to full sunlight. Brief exposure of leaves to HCN (to inhibit photoassimilation and photorespiration) also decreased electron transport drastically compared to electron transport in unpoisoned leaves with blocked stomata. Non-photochemical fluorescence quenching and reduction of Q_A, the primary electron acceptor of photosystem II was increased by HCN-poisoning. Very similar observations were made when glyceraldehyde was used instead of HCN to inhibit photosynthesis and photorespiration. In HCN-poisoned leaves, residual electron transport increased linearly with temperature and showed early light saturation revealing characteristics of the Mehler reaction. During short exposure of these leaves to photon flux densities equivalent to 25% of sunlight, no or only little photoinactivation of photosystem II was observed. However, prolonged exposure to sunlight caused inactivation even though non-photochemical quenching of chlorophyll fluorescence was extensive. Simultaneously, oxidation of cellular ascorbate and glutathione increased. Inactivation of photosystem II was reversible in dim light and in the dark only after short times of exposure to sunlight. Glyceraldehyde was very similar to HCN in increasing the sensitivity of photosystem II in leaves to sunlight. We conclude from the observations that the electron transport permitted by the interplay of photoassimilatory and photorespiratory electron transport is essential to prevent the photoinactivation of photosynthetic electron transport. The Mehler and Asada reactions, which give rise to strong nonphotochemical fluorescence quenching, are insufficient to protect the chloroplast electron transport chain against photoinactivation.     

Susceptibility of green leaves and green flower petals of CAM orchid <Emphasis Type="Italic">Dendrobium</Emphasis> cv. Burana Jade to high irradiance under natural tropical conditions

Photosynthetic rates of green leaves (GL) and green flower petals (GFP) of the CAM plant Dendrobium cv. Burana Jade and their sensitivities to different growth irradiances were studied in shade-grown plants over a period of 4 weeks. Maximal photosynthetic O₂ evolution rates and CAM acidities [dawn/dusk fluctuations in titratable acidity] were higher in leaves exposed to intermediate sunlight [a maximal photosynthetic photon flux density (PPFD) of 500–600 μmol m⁻² s⁻¹] than in leaves grown under full sunlight (a maximal PPFD of 1 000–1 200 μmol m⁻² s⁻¹) and shade (a maximal PPFD of 200–250 μmol m⁻² s⁻¹). However, these two parameters of GFP were highest in plants grown under the shade and lowest in full sun-grown plants. Both GL and GFP of plants exposed to full sunlight had lower predawn F_v/F_m [dark adapted ratio of variable to maximal fluorescence (the maximal photosystem 2 yield without actinic irradiation)] than those of shade-grown plants. When exposed to intermediate sunlight, however, there were no significant changes in predawn F_v/F_m in GL whereas a significant decrease in predawn F_v/F_m was found in GFP of the same plant. GFP exposed to full sunlight exhibited a greater decrease in predawn F_v/F_m compared to those exposed to intermediate sunlight. The patterns of changes in total chlorophyll (Chl) content of GL and GFP were similar to those of F_v/F_m. Although midday F_v/F_m fluctuated with prevailing irradiance, changes of midday F_v/F_m after exposure to different growth irradiances were similar to those of predawn F_v/F_m in both GL and GFP. The decreases in predawn and midday F_v/F_m were much more pronounced in GFP than in GL under full sunlight, indicating greater sensitivity in GFP to high irradiance (HI). In the laboratory, electron transport rate and photochemical and non-photochemical quenching of Chl fluorescence were also determined under different irradiances. All results indicated that GFP are more susceptible to HI than GL. Although the GFP of Dendrobium cv. Burana Jade require a lower amount of radiant energy for photosynthesis and this plant is usually grown in the shade, is not necessarily a shade plant.     

Photosynthetic response of <Emphasis Type="Italic">Quercus ilex</Emphasis> L. plants grown on compost and exposed to increasing photon flux densities and elevated CO<Subscript>2</Subscript>

Quercus ilex plants grown on two different substrates, sand soil (C) and compost (CG), were exposed to photosynthetic photon flux densities (PPFD) at 390 and 800 μmol(CO₂) mol⁻¹ (C₃₉₀ and C₈₀₀). At C₈₀₀ both C and CG plants showed a significant increase of net photosynthetic rate (P _N) and electron transport rate (ETR) in response to PPFD increase as compared to C₃₉₀. In addition, at C₈₀₀ lower non-photochemical quenching (NPQ) values were observed. The differences between C₃₉₀ and C₈₀₀ were related to PPFD. The higher P _N and ETR and the lower dissipative processes found in CG plants at both CO₂ concentrations as compared to C plants suggest that substrate influences significantly photosynthetic response of Q. ilex plants. Moreover, short-term exposures at elevated CO₂ decreased nitrate photo-assimilation in leaves independently from substrate of growth.     

Photosynthetic acclimation to photon irradiance and its relation to chlorophyll fluorescence and carbon assimilation in the halotolerant green alga Dunaliella viridis

This work describes the long-term acclimation of the halotolerant microalga Dunaliella viridis to different photon irradiance, ranging from darkness to 1500 μmol m⁻² s⁻¹. In order to assess the effects of long-term photoinhibition, changes in oxygen production rate, pigment composition, xanthophyll cycle and in vivo chlorophyll fluorescence using the saturating pulse method were measured. Growth rate was maximal at intermediate irradiance (250 and 700 μmol m⁻² s⁻¹). The increase in growth irradiance from 700 to 1500 μmol m⁻² s⁻¹ did not lead to further significant changes in pigment composition or EPS, indicating saturation in the pigment response to high light. Changes in Photosystem II optimum quantum yield (F_v/F_m) evidenced photoinhibition at 700 and especially at 1500 μmol m⁻² s⁻¹. The relation between photosynthetic electron flow rate and photosyntetic O₂ evolution was linear for cultures in darkness shifting to curvilinear as growth irradiance increased, suggesting the interference of the energy dissipation processes in oxygen evolution. Carbon assimilation efficiencies were studied in relation to changes in growth rate, internal carbon and nitrogen composition, and organic carbon released to the external medium. All illuminated cultures showed a high capability to maintain a C:N ratio between 6 and 7. The percentage of organic carbon released to the external medium increased to its maximum under high irradiance (1500 μmol m⁻² s⁻¹). These results suggest that the release of organic carbon could act as a secondary dissipation process when the xanthophyll cycle is saturated. This revised version was published online in June 2006 with corrections to the Cover Date.     

In vivo photosynthetic electron transport does not limit photosynthetic capacity in phosphate-deficient sunflower and maize leaves

The effects of extreme phosphate (Pi) deficiency during growth on the contents of adenylates and pyridine nucleotides and the in vivo photochemical activity of photosystem II (PSII) were determined in leaves of Helianthus annuus and Zea mays grown under controlled environmental conditions. Phosphate deficiency decreased the amounts of ATP and ADP per unit leaf area and the adenylate energy charge of leaves. The amounts of oxidized pyridine nucleotides per unit leaf area decreased with Pi deficiency, but not those of reduced pyridine nucleotides. This resulted in an increase in the ratio of reduced to oxidized pyridine nucleotides in Pi-deficient leaves. Analysis of chlorophyll a fluorescence at room temperature showed that Pi deficiency decreased the efficiency of excitation capture by open PSII reaction centres (φ_e), the in vivo quantum yield of PSII photochemistry (φ_PSII) and the photochemical quenching co-efficient (q_P), and increased the non-photochemical quenching co-efficient (q_N) indicating possible photoinhibitory damage to PSII. Supplying Pi to Pi-deficient sunflower leaves reversed the long-term effects of Pi-deficiency on PSII photochemistry. Feeding Pi-sufficient sunflower leaves with mannose or FCCP rapidly produced effects on chlorophyll a fluorescence similar to long-term Pi-deficiency. Our results suggest a direct role of Pi and photophosphorylation on PSII photochemistry in both long-and short-term responses of photosynthetic machinery to Pi deficiency. The relationship between φ_PSII and the apparent quantum yield of CO₂ assimilation determined at varying light intensity and 21 kPa O₂ and 35 Pa CO₂ partial pressures in the ambient air was linear in Pi-sufficient and Pi-deficient leaves of sunflower and maize. Calculations show that there was relatively more PSII activity per mole of CO₂ assimilated by the Pi-deficient leaves. This indicates that in these leaves a greater proportion of photosynthetic electrons transported across PSII was used for processes other than CO₂ reduction. Therefore, we conclude that in vivo photosynthetic electron transport through PSII did not limit photosynthesis in Pi-deficient leaves of sunflower and maize and that the decreased CO₂ assimilation was a consequence of a smaller ATP content and lower energy charge which restricted production of ribulose, 1-5, bisphosphate, the acceptor for CO₂.     

Extension of a biochemical model for the generalized stoichiometry of electron transport limited C3 photosynthesis

The widely used steady‐state model of Farquhar et al. (Planta 149: 78–90, 1980) for C₃ photosynthesis was developed on the basis of linear whole‐chain (non‐cyclic) electron transport. In this model, calculation of the RuBP‐regeneration limited CO₂‐assimilation rate depends on whether it is insufficient ATP or NADPH that causes electron transport limitation. A new, generalized equation that allows co‐limitation of NADPH and ATP on electron transport is presented herein. The model is based on the assumption that other thylakoid pathways (the Q‐cycle, cyclic photophosphorylation, and pseudocyclic electron transport) interplay with the linear chain to co‐contribute to a balanced production of NADPH and ATP as required by stromal metabolism. The original model assuming linear electron transport limited either by NADPH or by ATP, predicts quantum yields for CO₂ uptake that represent the highest and the lowest values, respectively, of the range given by the new equation. The applicability of the new equation is illustrated for a number of C₃ crop species, by curve fitting to gas exchange data in the literature. In comparison with the original model, the new model enables analysis of photosynthetic regulation via the electron transport pathways in response to environmental stresses.     

The effects of spacer length on the fluorescence quantum yields of the benzofurazan compounds bearing a donor–acceptor system

We studied the effects of spacer length on the fluorescence quantum yields (Φ) of photoinduced electron transfer (PET) reagents, using nitrobenzoxadiazole (NBD) derivatives that have the –NMe₂ moiety and NBD–NH– fluorophore as electron donor (D) and electron acceptor (A), respectively. The Φ values were reduced as the spacer length became shorter (n ≤ 4; n is the number of methylene units of the spacer) and the fluorescence recovered by suppression of the PET process. It is necessary for the useful PET reagents to link D and A with a short spacer to obtain a difference in the Φ values between fluorescent ‘off‐state’ and ‘on‐state’. Copyright © 2002 John Wiley & Sons, Ltd.     

Photosynthetic Gas Exchange and Chlorophyll a Fluorescence of Three Wild Soybean Species in Response to NaCl Treatments

Responses of photosynthetic gas exchange and chlorophyll (Chl) a fluorescence of three wild soybeans, Glycine soja, G. tomentella, and G. tabacina occurring in different habitats of Taiwan, to four NaCl treatments, 0S, LS, MS, and HS (i.e. 0, 17, 51, and 85 mM NaCl) were compared. In G. soja following exposure to NaCl treatment for one month, the photon saturated photosynthetic rate (P _N), the ratio of variable to maximum fluorescence (F_v/F_m), the quantum yield of photosystem 2 (_PS2), and the electron transport rate (ETR) decreased dramatically. These reductions increased with increasing concentration of NaCl treatment. Plants of MS and HS treatments did not survive after extending the treatment to two months. Reductions in P _N, _PS2, and ETR (but not in F_v/F_m) were found in G. tabacina after two months of exposure to MS and HS treatments, but the reduction was not as severe as that in G. soja. In G. tomentella, significant reductions in P _N and g _s were found only in HS plants after two months of treatment, but no significant differences in F_v/F_m, _PS2, and ETR were found among plants of the four treatments. Thus the three wild soybeans in Taiwan have differentiated in their photosynthetic susceptibility to salinity, G. tomentella being the least susceptible, G. soja the most sensitive, and G. tabacina the intermediate. Different mechanisms are attributed to the inhibition effect of salinity on photosynthesis of the three species.