Very high CO2 reduces photosynthesis, dark respiration and yield in wheat

Although terrestrial CO2 concentrations, [CO2] are not expected to reach 1000 micromoles mol-1 for many decades, CO2 levels in closed systems such as growth chambers and glasshouses, can easily exceed this concentration. CO2 levels in life support systems in space can exceed 10000 micromoles mol-1 (1%). Here we studied the effect of six CO2 concentrations, from ambient up to 10000 micromoles mol-1, on seed yield, growth and gas exchange of two wheat cultivars (USU-Apogee and Veery-l0). Elevating [CO2] from 350 to 1000 micromoles mol-1 increased seed yield (by 33%), vegetative biomass (by 25%) and number of heads m-2 (by 34%) of wheat plants. Elevation of [CO2] from 1000 to 10000 micromoles mol-1 decreased seed yield (by 37%), harvest index (by 14%), mass per seed (by 9%) and number of seeds per head (by 29%). This very high [CO2] had a negligible, non-significant effect on vegetative biomass, number of heads m-2 and seed mass per head. A sharp decrease in seed yield, harvest index and seeds per head occurred by elevating [CO2] from 1000 to 2600 micromoles mol-1. Further elevation of [CO2] from 2600 to 10000 micromoles mol-1 caused a further but smaller decrease. The effect of CO2 on both wheat cultivars was similar for all growth parameters. Similarly there were no differences in the response to high [CO2] between wheat grown hydroponically in growth chambers under fluorescent lights and those grown in soilless media in a glasshouse under sunlight and high pressure sodium lamps. There was no correlation between high [CO2] and ethylene production by flag leaves or by wheat heads. Therefore, the reduction in seed set in wheat plants is not mediated by ethylene. The photosynthetic rate of whole wheat plants was 8% lower and dark respiration of the wheat heads 25% lower when exposed to 2600 micromoles mol-1 CO2 compared to ambient [CO2]. It is concluded that the reduction in the seed set can be mainly explained by the reduction in the dark respiration in wheat heads, when most of the respiration is functional and is needed for seed development.     

Reactivation of photosynthesis in the photoinhibited green alga Chlamydomonas reinhardtii: Role of dark respiration and of light

Effect of quality, quantity and minimum duration of light on the process of recovery was investigated in the photoinhibited cells of the green alga Chlamydomonas reinhardtii. Complete and rapid reactivation of photosynthesis took place in diffuse white light of 25 mol m^–2 s^–1. The recovery was partial (< 10%) in the dark. Far red (725 nm), red (660 nm) and blue light (480 nm) in the range of 10 to 75 mol m^–2 s^–1 did not enhance the process of reactivation. Photoinhibited cells incubated in dark for 15 min when exposed for 5 min to diffuse light (25 mol m^–2 s^–1) showed complete reactivation. Even exposure of 15 min dark incubated photoinhibited cells to photoinhibitory light (2500 mol m^–2 s^–1) for 5 s fully regained the photosynthesis. The study indicated a very precise and triggering effect of light in the process of reactivation. The dark respiratory inhibitor KCN and uncouplers FCCP and CCCP increased the susceptibility of C. reinhardtii to photoinhibition and also prevented photoinhibited cells to reactivate fully even after longer period of incubation under suitable reactivating conditions. Of the various possibilities envisaged to assign the role of dark respiration in recovery process, supply of ATP by mitochondrial respiration appeared sound and pertinent.Abbreviations CCCP- carbonyl cyanide m-chlorophenylhydrazone - D1- 32 kDa protein of PS II reaction center - FCCP- carbonyl cyanide p-(trifluoromethoxy)phenylhydrazone - KCN- potassium cyanide - PBQ- phenyl-p-benzoquinone - PFD- photon flux density - SHAM- salicylhydroxamic acid NBRI Research Publication No. 431.     

Triphenyltin inhibits photosynthesis and respiration in marine microalgae

Summary The effects of diphenyltin and triphenyltin (TPhT) on gross photosynthesis and respiration by the diatomSkeletonema costatum (Greville) Cleve and the chlorophyteDunaliella tertiolecta (Butscher) were investigated by measuring the rates of change of oxygen concentration in samples which were alternately illuminated unilluminated. Measurements were carried out for 90 min after organotin addition. Triphyltin at concentrations in the nM to M range inhibited photosynthesis and respiration in both ogranisms. Levels of TPhT inhibiting these processes were two to three orders of magnitude higher forD. tertiolecta than forS. costatum. Photosynthesis and respiration byD. tertiolecta were resistant to diphenyltin at concentrations up to its limit of solubility (0.84 mM). WithS. costatum, inhibitory levels of diphenyltin were one to two orders of magnitude higher than those for triphenyltin. Inhibition was often progressive over the period after organotin addition. This effect varied in intensity and was more noticeale with the more resistantD. tertiolecta. Comparison of our results with levels of organotins which have been obeserved by others in Mediterranean coastal waters indicate that environmental levels of TPhT could influence phytoplankton composition and dynamics.     

Influence of medium frequency light/dark cycles of equal duration on the photosynthesis and respiration of Chlorella pyrenoidosa

Chlorella pyrenoidosa was grown in three continuous cultures each receiving a different light regime during the light period of a diurnal cycle. Hourly samples taken during the light period were subjected to medium frequency light/dark oscillations of equal duration, ranging from 3 to 240 seconds. The oxygen consumption and production of each sample were measured with an oxygen electrode in a small oxygen chamber. Although the light/dark cycles had little overall influence on photosynthetic activity, the microalgae appeared to adapt to the light regime to which they were subjected. Large differences were found between the maximum chlorophyll-specific production rates (P _infmax ^supB ), the chlorophyll-specific production rates (P^B) and the respiration rates between the cultures and treated subsamples. Respiration rates increased during the light period, whilst P^B either increased, or had a mid light period minimum or maximum. The culture which received an hourly light oscillation during the light period had the highest P _infmax ^supB and lowest respiration rates, and it is suggested that these algae react as in nature, whereas either a sinusoidal or a block light pattern is unnatural. The latter light regime is commonly used in laboratory studies.     

Effect of photosynthesis on dark mitochondrial respiration in green cells

Green plant cells can generate ATP in both chloroplasts and mitochondria. Hence the effect of photosynthesis on dark mitochondrial respiration can be considered at a variety of levels. Turnover of ceitric acid cycle dehydrogenases, which is essential for supply of carbon skeletons for amino acid synthesis, seems to be largely unaffected during photosynthesis. The source of carbon for the anaplerotic function of the citric acid cycle in light is however, not known with certainty. NADH generated in these reactions is probably not oxidised via the mitochondrial electron transfer chain coupled to ATP synthesis. However, it may be oxidised by the alternative cyanide-insensitive pathway, exported to the cytosol via the oxaloacetate-malate dicarboxylate shuttle or directly utilised for cytosolic nitrate reduction. Oxidation of succinate via cytochrome oxidase may also be similarly inhibited in light. Whether increase in the cytosolic ATP/ADP ratio in light is responsible for the inhibition of mitochondrial electron transfer to O₂ is not clearly established, because the ATP/ADP ratio is reported to be already quite high in the dark. Effective collaboration between photophosphorylation and oxidative phosphorylation in order to maintain the cytosolic energy charge at a present high level is discussed.     

The effect of heat on photosynthesis,dark respiration and cellular ultrastructure of the arctic-alpine psychrophyte Ranunculus glacialis

Effects of high temperatures on the leaves of Ranunculus glacialis were studied in plants taken from sites located between 2400-2550 m in the Central Alps. Changes in CO2 exchange rates, in vivo chlorophyll fluorescence, and cellular ultrastructure were investigated during and after an experimental heat exposure. The earliest heat stress effect was inactivation of the net photosynthetic rate at 38-39 °C. Between 40-42 °C, disorders appeared in the photosynthetic apparatus and in the tonoplast. Heat shock granules were observed at 42 °C in chloroplasts, and at 44 °C also in mitochondria. In this temperature range, the dark respiration rate was reversibly enhanced, and an increased number of polyribosomes indicated repair after the primary injury. Above 44 °C, the degradation progress entered the phase of chronic impairment leading to irreversible damage at 45-46 °C. An unusually wide temperature range from the start of reversible photosynthetic inhibition to incipient necrosis indicated a pronounced heat sensitivity, particularly in cellular functions, of this arctic-alpine species.     

The effect of heat on photosynthesis, dark respiration and cellular ultrastructure of the arctic-alpine psychrophyte Ranunculus glacialis

Effects of high temperatures on the leaves of Ranunculus glacialis were studied in plants taken from sites located between 2400-2550 m in the Central Alps. Changes in CO2 exchange rates, in vivo chlorophyll fluorescence, and cellular ultrastructure were investigated during and after an experimental heat exposure. The earliest heat stress effect was inactivation of the net photosynthetic rate at 38-39 °C. Between 40-42 °C, disorders appeared in the photosynthetic apparatus and in the tonoplast. Heat shock granules were observed at 42 °C in chloroplasts, and at 44 °C also in mitochondria. In this temperature range, the dark respiration rate was reversibly enhanced, and an increased number of polyribosomes indicated repair after the primary injury. Above 44 °C, the degradation progress entered the phase of chronic impairment leading to irreversible damage at 45-46 °C. An unusually wide temperature range from the start of reversible photosynthetic inhibition to incipient necrosis indicated a pronounced heat sensitivity, particularly in cellular functions, of this arctic-alpine species. This revised version was published online in June 2006 with corrections to the Cover Date.     

The low-light reduction in the quantum yield of photosynthesis: potential errors and biases when calculating the maximum quantum yield

Photosynthesis-irradiance (P-E) curves are widely used to describe photosynthetic efficiency and potential. Contemporary models assume maximal photosynthetic quantum yield () at low irradiances. But P-E observations made with both oxygen evolution and carbon uptake techniques show that this is not always the case. Using new and published data in conjunction with modeling exercises, we demonstrate that regardless of the mechanism there can be reductions in at low irradiances that are not readily observable using conventional P-E analyses. We also show that analytical errors, such as inaccurate estimation of dark oxygen consumption or carbon uptake, can markedly affect the structure of -E curves with negligible effect on P-E curve structure. Whether from respiration `corrections' or other mechanisms, these deviations in at low light levels from the maximum quantum yield of photosynthesis (_max) can lead to significant errors (> 50%) in the estimation of the linear portion of the P-E curve and ultimately _max. Non-linear models of P-E, such as the rectangular hyperbola, quadratic, exponential and hyperbolic tangent that are commonly used to estimate the initial slope () of the P-E curve assume that is maximal at low light levels and therefore can err in the estimation of _max when is reduced at low light levels. Using a diverse data set of 622 P-E curves with a total of 7623 points, we show that although model skills are high (r ² = 0.96 ± 0.05, 0.97 ± 0.04, 0.97 ± 0.04 and 0.97 ± 0.04, respectively), a large fraction of the model-predicted _max differ by greater than 10% from true _max values (91%, 50%, 82% and 46%, respectively). Data from these observations and modeling exercises lead us to suggest that _max be determined by directly estimating the true maximum of a -E curve rather than using the more conventional methodology employing the initial slope of the P-E curve.This revised version was published online in October 2005 with corrections to the Cover Date.     

Effects of fruit thinning agents on apple tree canopy photosynthesis and dark respiration

Effects on photosynthesis of the fruit thinning agents naphthaleneaceticacid (NAA) and three commercial plant growth regulator formulations,naphthaleneacetic acid ('Rhodofix') and naphthaleneacetamide('Amidthin') and 2-chloroethylphosphonic acid('Ethrel')were evaluated with respect to the stress they impose on the fruit tree, usingthe alternate-bearing sensitive apple cv. 'Elstar'. This work wasbased on the hypothesis that plant stress in the form of large reductions inleaf photosynthesis are a pre-requisite for successful fruit thinning. A newtechnology was employed for continuous recording of tree canopyphotosynthesis, dark respiration and carbon balance of apple trees. This wasbased on six canopy chambers, which enclosed apple trees under naturalconditions in the field, with on-line measurements and continuous analysis ofCO₂ exchange and automated data acquisition. All employed thinningagents reduced whole tree canopy photosynthesis consistently by3–34% on the five days following their application, withphotosynthesis still declining thereafter in the case of the NAA and'Amid-thin' application. The reduction after application of either'Rhodofix' or 'Ethrel', declined within five days, suchthat most of the original photosynthetic potential was restored, indicatingacceptable phytotoxicity of these three plant growth regulators at theconcentrations used. The effects on dark respiration differed markedly. NAA and'Ethrel' increased dark respirationover-proportionally by up to 106%, whereas 'Amid-thin' and'Rhodofix' decreased it by up to 46%inthe first night after application, thereby drastically affecting the carbonbalance of the tree in opposite ways. These results are integrated into ahypothesis linking basipetal auxin transport, phloem loading, translocation anddeficiency of photoassimilates.     

Effects of water velocity on photosynthesis and dark respiration in submerged stream macrophytes

The effects of flow velocities on dark respiration and net photosynthesis of eight submerged stream macrophytes were examined in a laboratory oxygen chamber. The shoots/leaves were exposed to saturating free-CO₂ concentrations and were attached basally so that they could move in the flowing water. Net photosynthesis declined by 34–61% as flow velocity increased from 1 to 8.6cm s^?1, while dark respiration increased 2.4-fold over the same range. The increase in dark respiration could only account for between 19 and 67% of the decrease in net photosynthesis. The relationship between flow velocity (U) and net photosynthesis (P) was described by: P=b×U^a. The exponent, a, varied from -0.20 to –0.48 and showed a negative correlation to the surface: volume (SA: V) ratio of the plants, i.e. species with high SA: V ratio were more sensitive to flow. In contrast, net photosynthesis of plants firmly attached to a supporting frame was not significantly affected by increasing flow velocity. This result indicates that the physical stress imposed on the plants by agitation or stretching in the flowing water is a key factor for the observed response.     

The maximum quantum yield of phylopiankton photosynthesis in situ

Light-limited photosynthetic carbon incorportion is expectedto be directly proportional to the scalar quantum irradiance.The proportionality constant is , where _mis the maximum quantum yield (mol C Einstein^–1 absorbed)and $$\stackrel{\&macr;}{{\hbox{ k }}_{\hbox{ c }}}$$ isthe mean spectral absorption coefficient (m² mg^–1 chla). Recent efforts to evaluate of in situphytoplankton photosynthesis are variously flawed. Lack of evidenceof proportionality and lack of correction of cosine to scalarirradiance are common deficiencies. Most data, as we interpretthem, indicate values in the range 0.0003 – 0.0006 mol C m² Einstein1 abs mg1 chl a. New determinationsin lrondequoit Bay, New York, lie in this range. Most estimatesof at depth have been about 0.010 m² mg^–1chl a. Similar values are being obtained for total particulatesfrom lrondequoit Bay; whether detritus contributes significantlyis not yet known. Published data, in our view, all point tovalues of m in situ in the range 0.03–0.07 mol C Einstein^–1abs. Published values >0.10 are almost certainly due to imprecisionor systematic error. ^*This paper is the result of a study made at the Group for AquaticPrimary Productivity (GAP) First International Workshop heldat the Limnological Institute, University of Konstanz, in April1982.     

Quantum yield variation across the three pathways of photosynthesis: not yet out of the dark

The convergent quantum yield hypothesis (CQY) assumes that thermodynamics and natural selection jointly limit variation in the maximum energetic efficiency of photosynthesis in low light under otherwise specified conditions (e.g. temperature and CO(2) concentration). A literature survey of photosynthetic quantum yield (phi) studies in terrestrial plants from C(3), C(4), and CAM photosynthetic types was conducted to test the CQY hypothesis. Broad variation in phi values from C(3) plants could partially be explained by accounting for whether the measuring conditions were permissive or restrictive for photorespiration. Assimilatory quotients (AQ), calculated from the CO(2) phi:O(2) phi ratios, indicated that 49% and 29% of absorbed light energy was allocated to carbon fixation and photorespiration in C(3) plants, respectively. The unexplained remainder (22%) may represent diversion to various other energy-demanding processes (e.g. starch synthesis, nitrogen assimilation). Individual and cumulative effects of these other processes on photosynthetic efficiency are poorly quantified. In C(4) plants, little variation in phi values was observed, consistent with the fact that C(4) plants exhibit little photorespiration. As before, AQ values indicate that 22% of absorbed light energy cannot be accounted for by carbon fixation in C(4) plants. Among all three photosynthetic types, the phi of photosynthesis in CAM plants is the least studied, appears to be highly variable, and may present the greatest challenge to the CQY hypothesis. The high amount of energy diverted to processes other than carbon fixation in C(3) and C(4) plants and the poor characterization of photosynthetic efficiency in CAM plants are significant deficiencies in our otherwise robust understanding of the energetics of terrestrial photoautotrophy.     

Altitudinal changes in temperature responses of net photosynthesis and dark respiration in tropical bryophytes

Background and Aims

There is a conspicuous increase of poikilohydric organisms (mosses, liverworts and macrolichens) with altitude in the tropics. This study addresses the hypothesis that the lack of bryophytes in the lowlands is due to high-temperature effects on the carbon balance. In particular, it is tested experimentally whether temperature responses of CO₂-exchange rates would lead to higher respiratory carbon losses at night, relative to potential daily gains, in lowland compared with lower montane forests.

Methods

Gas-exchange measurements were used to determine water-, light-, CO₂- and temperature-response curves of net photosynthesis and dark respiration of 18 tropical bryophyte species from three altitudes (sea level, 500 m and 1200 m) in Panama.

Key Results

Optimum temperatures of net photosynthesis were closely related to mean temperatures in the habitats in which the species grew at the different altitudes. The ratio of dark respiration to net photosynthesis at mean ambient night and day temperatures did not, as expected, decrease with altitude. Water-, light- and CO₂-responses varied between species but not systematically with altitude.

Conclusions

Drivers other than temperature-dependent metabolic rates must be more important in explaining the altitudinal gradient in bryophyte abundance. This does not discard near-zero carbon balances as a major problem for lowland species, but the main effect of temperature probably lies in increasing evaporation rates, thus restricting the time available for photosynthetic carbon gain, rather than in increasing nightly respiration rates. Since optimum temperatures for photosynthesis were so fine tuned to habitat temperatures we analysed published temperature responses of bryophyte species worldwide and found the same pattern on the large scale as we found along the tropical mountain slope we studied.     

Role of dark respiration in photoinhibition of photosynthesis and its reactivation in the cyanobacterium Anacystis nidulans

Photoinhibition of photosynthesis and its reactivation was studied in the cyanobaterium A. nidulans in the presence of the respiratory inhibitor sodium azide, the uncouplers carbonyl cyanide p -(trifluoromethoxy)-phenylhydrazone (FCCP) and carbonyl cyanide m -chlorophenylhydrazone (CCCP) and the photosystem I elicitor phenazine methosulphate (PMS). Inhibition of dark respiration by azide increased the susceptibility of the cyanobacterium to photoinhibition. Both FCCP and CCCP also remarkably affected the process of photoinhibition in A. nidulans. The PMS at lower photoinhibitory light intensity partially protected A. nidulans from photoinhibition. The recovery from photoinhibition in the presence of azide or FCCP was slow and normal photosynthesis could not be resumed even after a longer period of incubation under suitable reactivating condition. Thus dark respiration has a key function in the process of photoinhibition of photosynthesis and its reactivation in the cyanobacterium A. nidulans.     

Seasonal correlations of specific leaf weight to net photosynthesis and dark respiration of apple leaves

Specific leaf weight (SLW), net photosynthesis (P _n ), and dark respiration (R _d ) of apple leaves were monitored for an entire growing season. Leaves were sampled from the canopy interior and periphery to provide a range of SLW. Leaf P _n was linearly correlated with SLW until mid-August, when P _n began to decline. During September the relationship between SLW and P _n was a quadratic. Leaf R _d and SLW were linearly correlated throughout the season. Leaf P _n and R _d were significantly correlated through most of the season, but the relationship was not always linear. Specific leaf weight appears to be a reliable index of the previous light environment of a leaf, but use to estimate P _n is probably limited to the first half of the season, because of increased variation after mid-August.Former Graduate Research Assistant (presently Assistant Professor, Department of Horticulture and Forestry, Rutgers University, Cook College, New Brunswick, NJ 08903, USA) and Associate Professor, respectively.     

Effects of ultraviolet-C radiation on net photosynthesis, transpiration and dark respiration of Spathiphyllum wallisii

Electric arc welding was suspected to have damaged about 25000 potted Spathiphyllum wallisii plants in a commercial greenhouse. Therefore, the effects of UV-C radiation, phytotoxic gases and smoke particles on some basic physiological processes and on growth of Spathiphyllum plants were investigated in a controlled environment. The phytotoxic gases (NO, NO₂, O₃), separately and in combination, were harmless at exposure concentrations (2 mg m⁻³) well above incident levels, for several hours. The smoke particles, mainly ZnO, Fe₂O₃ and MnO, did not disturb the root environment and plant growth, even at 25 g m⁻², which is approximately 400 times the calculated dose after the adverse incident. UV-C radiation from electric welding significantly reduced photosynthesis and transpiration shortly after exposure at 1 m (80 μW cm⁻² nm⁻¹ at 254 nm), while dark respiration was significantly increased. Effects at 3 m were less pronounced. The effect persisted for 2–4 days, after which recovery was complete. Further experiments with continuous measurement of gas exchange in whole plants confirmed that short-term UV-C radiation (Philips 30W germicidal tubes) dramatically affects photosynthesis, dark respiration and transpiration. Plants irradiated with more than 10 μW cm⁻² nm⁻¹ at 254 nm did not recover completely within the week of the experiments. The immediate effects of UV-C on photosynthesis is caused by stomatal closure. However, most effects are transient, and electric are welding does not appear to have caused the investigated damage.