Upland cotton (Gossypium hirsutum L.) can move leaves to track the sun throughout the day, so-called leaf diaheliotropic movement. This paper reports an experimental test of the hypothesis that leaf diaheliotropic movement in upland cotton can enhance carbon assimilation and not increase the risk of stress from high energy load. In this experiment, cotton leaves were divided into two groups: one was that leaves could track the sun freely; another was that leaves were retained to the horizontal position. The diaheliotropic leaves recorded higher incident irradiance than the restrained ones, especially in the morning and late afternoon. Compared with restrained leaves, diaheliotropic leaves were generally warmer throughout the day. As expected, diaheliotropic leaves had significantly higher diurnal time courses of net photosynthetic rate (PN) than restrained leaves, except during 14:00-18:00 of the local time. Higher instantaneous water-use efficiency (WUE) was observed in diaheliotropic leaves in the early morning and late afternoon than in the restrained leaves. During the given day, diaheliotropic and restrained leaves had similar diurnal time courses of recovery of maximal quantum yield of PSII photochemistry (Fv/Fm). Diaheliotropic leaves recorded lower or similar photochemical quenching coefficient (qp) than restrained leaves did throughout the day. These results suggest that cotton leaf diaheliotropic movement can improve carbon gain and water use efficiency and not intensify photoinhibition. and Y.-L. Zhang ... [et al.].
In leaves of the mangrove species Avicennia germinans (L.) L. grown in salinities from 0 to 40 ‰, fluorescence, gas exchange, and δ13C analyses were done. Predawn values of Fv/Fm were about 0.75 in all the treatments suggesting that leaves did not suffer chronic photoinhibition. Conversely, midday Fv/Fm values decreased to about 0.55-0.60 which indicated strong down-regulation of photosynthesis in all treatments. Maximum photosynthetic rate (Pmax) was 14.58 ± 0.22 µmol m-2 s-1 at 0 ‰ it decreased by 21 and 37 % in plants at salinities of 10 and 40 ‰, respectively. Stomatal conductance (gs) was profoundly responsive in comparison to Pmax which resulted in a high water use efficiency. This was further confirmed by δ13C values, which increased with salinity. From day 3, after salt was removed from the soil solution, Pmax and gs increased up to 13 and 30 %, respectively. However, the values were still considerably lower than those measured in plants grown without salt addition.
The ability to modulate photosynthesis is essential for plants to adapt to fluctuating growing conditions. Populus species show high tolerance to various and highly variable environments. To understand their response strategies against fluctuating environments, this study investigated the morphological and physiological differences of white poplar (Populus alba) leaves when grown in a phytotron, glasshouse, and field. Our results show that the palisade cells were elongated in the field, which would enhance intercellular CO2 exchange. Photosynthetic capacity was the highest in the field leaves, as shown by higher electron transport rates (1.8 to 6.5 times) and carbon assimilation rates (2.7 to 4.2 times). The decrease of PSI acceptor-side limitation and increase of PSI donor-side limitation suggests changes in PSI redox status may contribute to photoprotection. This plasticity of white poplar allows adjusting its structure and photosynthesis under fluctuating conditions, which may partly enable its outstanding tolerance against environmental changes.
We aimed to find out relations among nonphotochemical quenching (NPQ), gross photosynthetic rate (PG), and photoinhibition during photosynthetic light induction in three woody species (one pioneer tree and two understory shrubs) and four ferns adapted to different light regimes. Pot-grown plants received 100% and/or 10% sunlight according to their light-adaptation capabilities. After at least four months of light acclimation, CO2 exchange and chlorophyll fluorescence were measured simultaneously in the laboratory. We found that during light induction the formation and relaxation of the transient NPQ was closely related to light intensity, light-adaption capability of species, and PG. NPQ with all treatments increased rapidly within the first 1-2 min of the light induction. Thereafter, only species with high PG and electron transport rate (ETR), i.e., one pioneer tree and one mild shade-adapted fern, showed NPQ relaxing rapidly to a low steady-state level within 6-8 min under PPFD of 100 μmol(photon) m-2 s-1 and ambient CO2 concentration. Leaves with low PG and ETR, regardless of species characteristics or inhibition by low CO2 concentration, showed slow or none NPQ relaxation up to 20 min after the start of low light induction. In contrast, NPQ increased slowly to a steady state (one pioneer tree) or it did not reach the steady state (the others) from 2 to 30 min under PPFD of 2,000 μmol m-2 s-1. Under high excess of light energy, species adapted to or plants acclimated to high light exhibited high NPQ at the initial 1 or 2 min, and showed low photoinhibition after 30 min of light induction. The value of fastest-developing NPQ can be quickly and easily obtained and might be useful for physiological studies., S.-L. Wong, M.-Y. Huang, C.-W. Chen, J.-H. Weng., and Obsahuje bibliografii
Two clones of Hevea brasiliensis (RRII 105 and PB 235) were grown for one year in two distinct agroclimatic locations (warmer and colder, W and C) in peninsular India. We simultaneously measured gas exchange and chlorophyll (Chl) fluorescence on fully mature intact leaves at different photosynthetic photon flux densities (PPFDs) and ambient CO2 concentrations (Ca) and at constant ambient O2 concentration (21 %). Net photosynthetic rate (PN), apparent quantum yield for CO2 assimilation (Φc), in vivo carboxylation efficiency (CE), and photosystem 2 quantum yield (ΦPS2) were low in plants grown in C climate and these reductions were more predominant in RRII 105 than in PB 235 which was also reflected in their growth. We estimated in these clones the partitioning of photosynthetic electrons between CO2 reduction (JA) and processes other than CO2 reduction (J*) at low and high PPFDs and Ca. At high Ca (700 µmol mol-1) most of the photosynthetic electrons were used for CO2 assimilation and negligible amount went for other processes when PPFD was low (200-300 µmol m-2 s-1) both in the C and W climates. But at high PPFD (900-1 100 µmol m-2 s-1), J* was appreciably high even at a high Ca. Hence at normal ambient Ca and high irradiance, electrons can be generated in the photosynthetic apparatus far in excess of what can be safely utilised for photosynthetic CO2 reduction. However, at high Ca there was increased diversion of electrons to photosynthetic CO2 reduction which resulted in improved photosynthetic parameters even in plants grown in C climate. and B. Alam, D. B. Nair, J. Jacob.
Photoinactivation of photosystem 2 (PS2) results from absorption of so-called "excessive" photon energy. Chlorophyll a fluorescence can be applied to quantitatively estimate the portion of excessive photons by means of the parameter E = (F - F0')/Fm', which reflects the share of the absorbed photon energy that reaches the reaction centers (RCs) of PS2 complexes with QA in the reduced state ('closed' RCs). Data obtained for cotton (Gossypium hirsutum), bean (Phaseolus vulgaris), and arabidopsis (Arabidopsis thaliana) suggest a linear relationship between the total amount of the photon energy absorbed in excess (excessive irradiation) and the decline in PS2 activity, though the slope may differ depending on the species. This relationship was sensitive not only to the leaf temperature but also to treatment with methyl viologen. Such observations imply that the intensity of the oxidative stress as well as the plant's ability to detoxify active oxygen species may interact to determine the damaging potential of the excessive photons absorbed by PS2 antennae. Energy partitioning in PS2 complexes was adjusted during adaptation to irradiation and in response to a decrease in leaf temperature to minimize the excitation energy that is trapped by 'closed' PS2 RCs. The same amount of the excessive photons absorbed by PS2 antennae led to a greater decrease in PS2 activity at warmer temperatures, however, the delay in the development of non-photochemical and photochemical energy quenching under lower temperature resulted in faster accumulation of excessive photons during induction. Irradiance response curves of EF suggest that, at high irradiance (above 700 μmol m-2 s-1), steady-state levels of this parameter tend to be similar regardless of the leaf temperature. and D. Kornyeyev, A. S. Holaday, B. A. Logan.
a1_Shallow ponds with rapidly photosynthesising cyanobacteria or eukaryotic algae are used for growing biotechnology feedstock and have been proposed for biofuel production but a credible model to predict the productivity of a column of phytoplankton in such ponds is lacking. Oxygen electrodes and Pulse Amplitude Modulation (PAM) fluorometer technology were used to measure gross photosynthesis (PG) vs. irradiance (E) curves (PG vs. E curves) in Chlorella (chlorophyta), Dunaliella salina (chlorophyta) and Phaeodactylum (bacillariophyta). PG vs. E curves were fitted to the waiting-in-line function [PG = (PGmax × E/Eopt) × exp(1 — E/Eopt)]. Attenuation of incident light with depth could then be used to model PG vs. E curves to describe PG vs. depth in pond cultures of uniformly distributed planktonic algae. Respiratory data (by
O2-electrode) allowed net photosynthesis (PN) of algal ponds to be modelled with depth. Photoinhibition of photosynthesis at the pond surface reduced PN of the water column. Calculated optimum depths for the algal ponds were: Phaeodactylum, 63 mm; Dunaliella, 71 mm and Chlorella, 87 mm. Irradiance at this depth is ≈ 5 to 10 μmol m-2 s-1 photosynthetic photon flux density (PPFD). This knowledge can then be used to optimise the pond depth. The total net P N [μmol(O2) m-2 s-1] were: Chlorella, ≈ 12.6 ± 0.76; Dunaliella, ≈ 6.5 ± 0.41; Phaeodactylum ≈ 6.1 ± 0.35. Snell’s and Fresnel’s laws were used to correct irradiance for reflection and refraction and thus estimate the time course of PN over the course of a day taking into account respiration during the day and at night. The optimum PN of a pond adjusted to be of optimal depth (0.1-0.5 m) should be approximately constant because increasing the cell density will proportionally reduce the optimum depth of the pond and vice versa., a2_Net photosynthesis for an optimised pond located at the tropic of Cancer would be [in t(C) ha-1 y-1]: Chlorella, ≈ 14.1 ± 0.66; Dunaliella, ≈ 5.48 ± 0.39; Phaeodactylum, ≈ 6.58 ± 0.42 but such calculations do not take weather, such as cloud cover, and temperature, into account., R. J. Ritchie, A. W. D. Larkum., and Obsahuje bibliografii a dodatky
Irradiance data software developed by the NREL Solar Radiation Laboratory (Simple Model of Atmospheric Radiative Transfer of Sunshine, SMARTS) has been used for modelling photosynthesis. Spectra and total irradiance were expressed in terms of quanta [mol m-2 s-1, photosynthetic photon flux density, PPFD (400-700 nm)]. Using the SMARTS software it is possible to (1) calculate the solar spectrum for a planar surface for any given solar elevation angle, allowing for the attenuating effects of the atmosphere on extraterrestrial irradiance at each wavelength in the 400-700 nm range and for the thickness of atmosphere the light must pass through during the course of a day, (2) calculate PPFD vs. solar time for any latitude and date and (3) estimate total daily irradiance for any latitude and date and hence calculate the total photon irradiance for a whole year or for a growing season. Models of photosynthetic activity vs. PPFD are discussed. Gross photosynthesis (Pg) vs. photosynthetic photon flux density (PPFD) (Pg vs. I) characteristics of single leaves compared to that of a canopy of leaves are different. It is shown that that the optimum irradiance for a leaf (Iopt) is the half-saturation irradiance for a battery of leaves in series. A C3 plant, with leaves having an optimum photosynthetic rate at 700 μmol m-2 s-1 PPFD, was used as a realistic worked example. The model gives good estimates of gross photosynthesis (Pg) for a given date and latitude. Seasonal and annual estimates of Pg can be made. Taking cloudiness into account, the model predicts maximum Pg rates of about 10 g(C) m-2 d-1, which is close to the maximum reported Pg experimental measurements. and R. J. Ritchie.
This study was performed to evaluate the ecophysiological acclimation of Catalpa bungei plantlets to different light conditions. We hypothesized that the acclimation of old and newly developed leaves to both increasing and decreasing irradiance should follow different patterns. The growth, photosynthesis, chlorophyll (Chl) content, and Chl fluorescence response were examined over a range of light treatments. The plants were grown under fixed light intensities of 80% (HH), 50% (MM), 30% (LL) of sun light and transferring irradiance of 80% to 50% (HM), 80% to 30% (HL), 30% to 50% (LM) and 30% to 80% (LH). For old leaves, light-saturation point, photosynthetic capacity, dark respiration rate of LH were lower than that of HH, while HL were higher than LL, indicating that light-response parameters were affected by the original growth light environment. Initial fluorescence increased and variable fluorescence decreased in LH and LM after transfer, and the PSII damage was more serious in LH than that in LM, and could not recover within 30 d. It suggested that the photoinhibition damage and recovery time in old leaves was related to the intensity of light after transfer. For the newly emerged leaves with leaf primordia formed under the same light environment, a significant difference was observed in leaf morphology and pigment contents, suggesting that previous light environment exhibited carry-over effect on the acclimation capacity to a new light environment. Our result showed that thinning and pruning intensity should be considered in plantation management, because great changes in light intensity may cause photoinhibition in shade-adapted leaves., J. W. Wu, Y. Su, J. H. Wang, Q. He, Q. Qiu, J. W. Ma, J. Y. Li., and Obsahuje bibliografii
The review deals with thermal dissipation of absorbed excitation energy within pigment-protein complexes of thylakoid membranes in higher plants. We focus on the de-excitation regulatory processes within photosystem 2 (PS2) that can be monitored as non-photochemical quenching of chlorophyll (Chl) a fluorescence consisting of three components known as energy-dependent quenching (qE), state-transition quenching (qT), and photoinhibitory quenching (qI). We summarize the role of thylakoid lumen pH, xanthophylls, and PS2 proteins in qE mechanism. Further, both the similarity between qE and qI and specific features of qI are described. The other routes of thermal energy dissipation are also mentioned, that is dissipation within photosystem 1 and dissipation through the triplet Chl pathway. The significance of the individual de-excitation processes in protection against photo-oxidative damage to the photosynthetic apparatus under excess photon supply is stretched. and M. Štroch, V. Špunda, I. Kurasová.