Cadmium toxicity and translocation in rice seedlings are reduced by hydrogen peroxide pretreatment

A hydroponic experiment was carried out to study the role of hydrogen peroxide (H₂O₂) in enhancing tolerance and reducing translocation of cadmium (Cd) in rice seedlings. Plant growth (length and biomass of shoot and root) was significantly repressed by Cd exposure. However, pretreatment with 100 μM H₂O₂ for 1d mitigated Cd stress by inducing enzyme activities for antioxidation (e.g., superoxide dismutase (SOD), catalase (CAT), guaiacol peroxidase (GPX), ascorbate peroxidase (APX)) and detoxification (e.g., glutathione S-transferase (GST)) as well as by elevating contents of reduced glutathione (GSH) and ascorbic acid (AsA). As a result, H₂O₂ and malondialdehyde (MDA) content decreased in plants and the seedling growth was less inhibited. On the other hand, H₂O₂ pretreatment decreased Cd concentration in shoots, thus lowered the ratio of Cd concentration in shoots and roots (S/R), indicating that H₂O₂ may affect Cd distribution in rice seedlings. The improved Cd tolerance is partly due to an enhanced antioxidative system that efficiently prevents the accumulation of H₂O₂ during Cd stress. Increased Cd sequestration in rice roots may contribute to the decline of Cd translocation.     

Facile and greener hydrothermal honey-based synthesis of Fe3O 4/Au core/shell nanoparticles for drug delivery applications

In the present research, we report a greener, faster, and low-cost synthesis of gold-coated iron oxide nanoparticles (Fe₃O₄/Au-NPs) by different ratios (1:1, 2:1, and 3:1 molar ratio) of iron oxide and gold with natural honey (0.5% w/v) under hydrothermal conditions for 20 minutes. Honey was used as the reducing and stabilizing agent, respectively. The nanoparticles were characterized by X-ray diffraction (XRD), UV-visible spectroscopy, field emission scanning electron microscope (FESEM), energy-dispersive X-ray spectroscopy (EDXS), transmission electron microscopy (TEM), selected area electron diffraction (SAED), vibrating sample magnetometer (VSM), and fourier transformed infrared spectroscopy (FT-IR). The XRD analysis indicated the presence of Fe₃O₄/Au-NPs, while the TEM images showed the formation of Fe₃O₄/Au-NPs with diameter range between 3.49 nm and 4.11 nm. The VSM study demonstrated that the magnetic properties were decreased in the Fe₃O₄/Au-NPs compared with the Fe₃O₄-NPs. The cytotoxicity threshold of Fe₃O₄/Au-NPs in the WEHI164 cells was determined by using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. It was demonstrated no significant toxicity in higher concentration up to 140.0 ppm which can become the main candidates for biological and biomedical applications, such as drug delivery.     

广西典型红壤旱地施用钙镁磷肥对玉米产量及其镉累积的影响

在广西典型类型红壤旱地布置玉米磷肥施用量的田间试验,研究不同钙镁磷肥施用量(磷肥Cd含量为0.0651 mg/kg)对玉米产量及地上部Cd累积的影响。结果表明,与不施磷肥处理(CK)相比,施磷肥可分别显著提高春、秋玉米籽粒产量8.2%—13.1%和13.7%—20.0%。高磷(600 kg P2O5/hm2)处理的春玉米秸秆产量比CK显著提高11.4%;施磷处理春、秋玉米秸秆Cd含量分别下降2.7%—45.8%和11.0%—43.6%;而籽粒Cd含量分别下降13.0%—40.6%和9.9%—31.5%,且秸秆和籽粒的Cd含量及累积量均随施磷量的增加而逐渐降低,其中以高磷处理最为显著。玉米秸秆及籽粒Cd累积量在高磷处理下(600 kg P2O5/hm2)分别比低磷处理(75—300 kg P2O5/hm2)降低13.6%—41.5%和8.8%—29.3%。相关分析表明,玉米Cd含量与土壤pH呈显著负相关,与土壤有效Cd含量呈显著正相关。施磷提高土壤pH,而降低土壤有效Cd含量。高量磷肥施用降低土壤Cd的有效性进而降低玉米对Cd的吸收累积。     

Luminescence studies on Al4B2O9:Eu2+ phosphor crystals

A novel blue‐emitting phosphor, Eu²⁺‐doping Al₄B₂O₉, was prepared via a modified solid‐state reaction. Al₄B₂O₉:Eu²⁺ nanoparticles with diameters varying in a range from 20 to 50 nm were obtained using urea as an auxiliary reagent at the optimum temperature of 850°C. The crystallization and particle sizes of Al₄B₂O₉:Eu²⁺ were investigated using powder X‐ray diffraction (XRD) and transmission electron microscopy (TEM). Photoluminescence (PL) results showed that Al₄B₂O₉:Eu²⁺ phosphor could be efficiently excited by the ultraviolet region from 240 to 410 nm, exhibiting bright blue emission. Further investigation on concentration‐dependent emission spectra indicated that the Al_3.997B₂O₉:Eu²⁺_0.003 phosphor exhibited the strongest luminescent, and the relative PL intensity decreased with increasing Eu²⁺ concentration due to concentration quenching. In addition, the concentration quenching for the one‐Eu‐site emission centers was caused by the electric multipole–multipole interaction. Copyright © 2010 John Wiley & Sons, Ltd.     

Role of Li+ ions on the surface morphology and thermoluminescence properties of Y2O3:Tm3+ nanophosphor

Y₂O₃:Tm³⁺ and Li⁺ co‐doped Y₂O₃:Tm³⁺ nanopowders were synthesized using the solution combustion method for possible application in ultraviolet (UV) light dosimetry. X‐ray diffraction revealed the crystallite sizes to be in the range 21–44 nm and 30–121 nm using the Scherrer equation and the W‐H plot relationship, respectively. Field emission scanning electron microscopy confirmed that, after co‐doping with 4 mol% concentration of Li⁺, the particles were spherical in nature with an average size of ~30 nm. Fourier transformed infrared spectroscopy results showed bands at wavenumbers of 556, 1499, 1704, 2342, 2358, 2973, 3433, and 3610 cm^?1 that corresponded to the stretching and bending vibrations of Y–O, C=O and O–H. Thermoluminescence (TL) glow peaks for Y₂O₃:Tm³⁺ nanophosphors observed at 399 and 590 K were attributed to oxygen defects caused using UV irradiation. These oxygen defects firstly resulted in an increased prominent peak TL intensity for up to 270 min of irradiation and then a decrease. This was attributed to the presence of oxygen defect clusters that caused a reduction in recombination centres. The Li⁺ co‐doped sample showed peaks at 356, 430, and 583 K and its intensity sublinearly increased up to 90 min and then thereafter decreased. The TL trapping parameters were calculated using computerized glow curve deconvolution methods. The Li⁺ co‐doped sample exhibited less fading and high trap density under the UV radiation.     

Comparative study of metal uptake by Eichhornia crassipes growing in ponds from mining and nonmining areas—a field study

The study deals with metal (Cu, Mn, Pb, Cd) concentrations in sediment, water, and corresponding leaf samples of Eichhornia crassipes obtained from ponds in nonmining (P1) and mining (P2, P3, P4) regions. In spite of significant high metal concentrations in sediments from mining regions rather than from nonmining regions, the unelevated SQG-I (sediment quality guideline index) values proved low levels of toxicity. Irrespective of the wide range of metal concentration in sediments, the levels in water had been nearly consistent in all the ponds. Concentration of metals in leaves decreased with an increase in concentration in the substrate. Mn, Cu, and Cd accumulated within the range of MAC (maximum allowable concentration) for plants, whereas Pb accumulated above the limit. BAF_sl (bioaccumulation factor with respect to sediment) values for Mn (0.20–0.27) were highest, followed by Cu (0.13–0.20) and Pb (0.03–0.20), whereas BAF_wl (bioaccumulation factor with respect to water) was highest for Cu (428–3205), followed by Mn (285–1100), Pb (242–506), and Cd (7–130). This study concludes that E. crassipes plays a very important role in removing the metals from the pond ecosystem, whereas leaves of this plant can be used effectively for biomonitoring surveys. E. crassipes can be used for phytoremediation of polluted wetlands through proper management strategies.     

土壤不同镉水平对马缨丹生长及其抗氧化酶活性的影响

采用盆栽试验方法,分别设置0(对照,不添加镉)、30、60、90、120、150、180、210mg·kg-1共8个土壤镉处理水平,研究土壤不同镉水平对马缨丹(Lantana comara L.)生长及其抗氧化酶活性的影响,以探讨马缨丹对镉胁迫的生理响应机制。结果显示:(1)随着土壤镉处理浓度的升高,马缨丹干重呈先升高后降低的趋势,30mg·kg-1镉处理能促进植株的生长,而浓度高于60mg·kg-1时显著抑制马缨丹的生长。(2)马缨丹叶片和根系中O-·2产生速率、H2O2和MDA含量及电解质渗漏率均随土壤镉处理浓度的升高和胁迫时间的延长逐渐升高,胁迫90d时,叶片和根系中O-·2产生速率、H2O2和MDA含量及电解质渗漏率分别在镉浓度高于60和30mg·kg-1时显著低于对照。(3)叶片和根系抗氧化酶SOD、POD、APX和CAT活性随着土壤镉处理浓度的增加大体呈先升高后降低的趋势,并在镉浓度分别高于90和60mg·kg-1时,叶片和根系抗氧化酶活性显著低于对照。研究表明,低浓度镉处理土壤能促进马缨丹植株生长,而高浓度镉处理土壤显著降低了马缨丹体内抗氧化酶活性,导致活性氧大量积累,引起严重的膜脂过氧化伤害,从而显著抑制马缨丹植株的生长。     

Cadmium effects on mineral nutrition and stress in <Emphasis Type="Italic">Potamogeton crispus</Emphasis>

The mechanisms of plant tolerance to cadmium stress were studied by short-term exposure of Potamogeton crispus L. to various concentrations of Cd ranging from 0 to 0.09 mM. The accumulation of Cd and its influence on nutrient elements, chlorophyll pigments, ultrastructure, proline and MDA contents, and free radical production, as well as the activities of superoxide dismutase (SOD), peroxidase (POD), ascorbate peroxidase (APX), and glutathione reductase (GR) were investigated. The higher Cd concentration in the medium resulted in a significant enhancement of Cd accumulation. Photosynthetic pigment content decreased and ultrastructural damage to the leaf cells was aggravated with the increase in the Cd concentrations. Disruption of chloroplasts and mitochondria was observed even at the lowest concentration of Cd. Meantime, the rate of O₂^*− generation and the contents of H₂O₂ and MDA significantly increased under Cd stress, suggesting that Cd caused oxidative stress. In addition, the antioxidant system was clearly activated following Cd exposure. SOD and POD activities increased initially and then decreased, while APX and GR activities markedly increased. Simultaneously, mineral nutrition was disturbed. While K, P, Ca, and Cu contents decreased, Na, Fe, and Mn contents increased. Induction of antioxidant enzyme activities in leaves exposed to elevated Cd concentrations may be involved in Cd tolerance of P. crispus.     

Characterization of laser produced plasma using laser induced breakdown spectroscopy

The plasma parameter studies of the Nd:YAG (neodymium-doped yttrium aluminum garnet, Nd:Y₃Al₁₅O₁₂) crystal by using the fundamental (1064 nm) and second (532 nm) harmonics of Nd:YAG laser are reported. The electron temperature (T _e ) and electron number density (N _e) were determined using the Boltzmann plot method and the Stark-broadened line profile, respectively. An increase in the plasma parameters have been observed with an increase in the laser irradiance for both laser modes. The electron temperatures were calculated in the range of 0.53–0.66 eV for 1064 nm and 0.47–0.60 eV for 532 nm, and the electron number densities were determined in the range of 7.43 × 10¹⁵–3.27 × 10¹⁶ cm^?3 for 1064 nm and 1.35 × 10¹⁶–3.97 × 10¹⁶ cm^?3 for 532 nm in the studied irradiance range of 1.19–12.5 GW/cm². However, the spatial evolution of the plasma parameters investigated up to 2.75 mm away from the target surface at a fixed laser irradiance of 6.51 GW/cm2 showed a decreasing trend. In addition, the estimated values of the inverse bremsstrahlung (IB) absorption coefficients at both laser wavelengths showed that the IB process is dominant for the 1064-nm laser.     

Hydrogen Peroxide-Mediated Growth of the Root System Occurs via Auxin Signaling Modification and Variations in the Expression of Cell-Cycle Genes in Rice Seedlings Exposed to Cadmium Stress

The link between root growth, H₂O₂, auxin signaling, and the cell cycle in cadmium (Cd)‐stressed rice (Oryza sativa L. cv. Zhonghua No. 11) was analyzed in this study. Exposure to Cd induced a significant accumulation of Cd, but caused a decrease in zinc (Zn) content which resulted from the decreased expression of OsHMA9 and OsZIP. Analysis using a Cd‐specific probe showed that Cd was mainly localized in the meristematic zone and vascular tissues. Formation and elongation of the root system were significantly promoted by 3‐amino‐1,2,4‐triazole (AT), but were markedly inhibited by N,N’‐dimethylthiourea (DMTU) under Cd stress. The effect of H₂O₂ on Cd‐stressed root growth was further confirmed by examining a gain‐of‐function rice mutant (carrying catalase1 and glutathione‐S‐transferase) in the presence or absence of diphenylene iodonium. DR5‐GUS staining revealed close associations between H₂O₂ and the concentration and distribution of auxin. H₂O₂ affected the expression of key genes, including OsYUCCA, OsPIN, OsARF, and OsIAA, in the auxin signaling pathway in Cd‐treated plants. These results suggest that H₂O₂ functions upstream of the auxin signaling pathway. Furthermore, H₂O₂ modified the expression of cell‐cycle genes in Cd‐treated roots. The effects of H₂O₂ on root system growth are therefore linked to auxin signal modification and to variations in the expression of cell‐cycle genes in Cd‐stressed rice. A working model for the effects of H₂O₂ on Cd‐stressed root system growth is thus proposed and discussed in this paper.     

Radiosensitization effects by bismuth oxide nanorods of different sizes in megavoltage external beam radiotherapy

BackgroundNanotechnology application has successfully reached numerous scientific breakthroughs including in radiotherapy. However, the clinical application of nanoparticles requires more diligent research primarily on the crucial parameters such as nanoparticle sizes. This study is aimed to investigate the influence of bismuth oxide nanorod (Bi₂O₃-NR) sizes on radiosensitization effects on MCF-7 and HeLa cell lines for megavoltage photon and electron beam radiotherapy.Materials and methodsMCF-7 and HeLa cells were treated with and without 0.5 μMol/L of Bi₂O₃-NR of varying sizes (60, 70, 80, and 90 nm). The samples, including the control groups, were exposed to different radiation doses (0–10 Gy), using photon (6 MV and 10 MV), and electron beam (6 MeV and 12 MeV) radiotherapy. Clonogenic assay was performed, and sensitization enhancement ratio (SER) was determined from linear quadratic based cell survival curves.ResultsThe results depicted that 60 nm Bi₂O₃-NR yields the most excellent SER followed by 70 nm Bi₂O₃-NR. Meanwhile, the 80 and 90 nm Bi₂O₃-NR showed an insignificant difference between treated and untreated cell groups. This study also found that MCF-7 was subjected to more cell death compared to HeLa.Conclusion60 nm Bi₂O₃-NR was the optimal Bi₂O₃-NR size to induce radiosensitization effects for megavoltage external beam radiotherapy. The SER in photon beam radiotherapy marked the highest compared to electron beam radiotherapy due to decreased primary radiation energy from multiple radiation interaction and higher Compton scattering.     

Effects of Cadmium on Enzymatic and Non-Enzymatic Antioxidative Defences of Rice (Oryza Sativa L.)

The effects of 60-d cadmium (Cd) exposure on enzymatic and non-enzymatic antioxidative system of Oryza sativa L. seedlings at tillering stage were studied using soil culture experiment. Research findings showed that chlorophyll content of Oryza sativa L. declined with the increase in soil metal concentration. Cd pollution induced the antioxidant stress by inducing O₂ ^?1 and H₂O₂, which increased in plants; at the same time, MDA as the final product of peroxidation of membrane lipids, accumulated in plant. The antioxidant enzyme system was initiated under the Cd exposure, i.e. almost all the activities of superoxide dismutase (SOD), peroxidase, catalase, glutathione peroxidase, and ascorbate peroxidase were elevated both in leaves and roots. The non-protein thiols including phytochelatins and glutathione to scavenge toxic free radicals caused by Cd stress was also studied. The contents of phytochelatins and glutathione were about 3.12–6.65-fold and 3.27–10.73-fold in leaves, against control; and the corresponding values were about 3.53–9.37-fold and 1.41–5.11-fold in roots, accordingly.     

Luminescence properties of novel deep‐red‐emitting Ca3Al2Ge2O10:Cr3+ phosphors

Ca₃Al₂Ge₂O₁₀:Cr³⁺ phosphors were prepared by a high‐temperature solid‐state method, and their luminescence properties were investigated. Under excitation at 550 nm, Ca₃Al₂Ge₂O₁₀:Cr³⁺ phosphors exhibited a broad red emission band at 697 nm in the range 650–750 nm that was caused by the ²E→⁴A₂ transition of Cr³⁺. For the 697 nm emission peak, emission intensity reached a maximum at x = 0.07, and there was concentration quenching of Cr³⁺ in Ca₃Al₂Ge₂O₁₀; the corresponding concentration quenching mechanism was analysed. Under excitation at 262 nm, the Ca₃Al₂Ge₂O₁₀:Cr³⁺ phosphor showed a weakly broad emission band in the range 350–600 nm that was caused by intrinsic defects (V′′_Ca and V′′_O). Copyright © 2016 John Wiley & Sons, Ltd.     

Inhibition of inorganic carbon transport by oxygen in a high CO2-requiring mutant (E1) of Anacystis nidulans R2

The effect of O₂ on inorganic carbon (C_i) transport was studied with a high CO₂-requiring mutant (E₁) of Anacystis nidulans R₂. Oxygen (above 2%) inhibited C_i transport by 15–35|X% at CO₂ concentrations above 200 μl/l, but had no apparent effect at low, limiting CO₂ concentration. The action spectra for C_i transport measured in the presence or absence of 20% O₂ showed two peaks around 684 and 625 nm, corresponding to chlorophyll a and phycocyanin absorption, respectively. The difference between these two spectra (anaerobic minus aerobic) showed one peak around 625 nm, which indicates that a linear electron transport from water to O₂ is involved in the O₂ inhibition of C_i transport. Dithiothreitol could overcome the inhibition by O₂. The results suggested that the O₂ inhibition is a result of inactivation of the C_i-transporting system.     

A novel hydrogen peroxide sensor based on immobilization of haemoglobin on nano-TiO2/DTAB composite film

Abstract

The direct electron transfer of immobilized haemoglobin (Hb) on nano-TiO₂ and dodecyltrimethylammonium bromide (DTAB) film modified carbon paste electrode (CPE) and its application as a hydrogen peroxide (H₂O₂) biosensor were investigated. On nano-TiO₂/DTAB/Hb/CPE, Hb displayed a rapid electron transfer process with participation of one proton and with an electron transfer rate constant which estimated as 0.29 s^??1. Thus, the proposed biosensor exhibited a high sensitivity and excellent electrocatalytic activity for the reduction of H₂O₂. The catalytic reduction current of H₂O₂ was proportional to H₂O₂ concentration in the range of 0.2–4.0 mM with a detection limit of 0.07 mM. The apparent Michaelis–Menten constant (K_m^app) of the biosensor was calculated to be 0.127 mM, exhibiting a high enzymatic activity and affinity. This sensor for H₂O₂ can potentially be applied in determination of other reactive oxygen species as well.     

High nitrate removal by starch‐stabilized Fe0 nanoparticles in aqueous solution in a controlled system

This study was conducted to investigate biodenitrification efficiency with starch‐stabilized nano zero valent iron (S‐nZVI) as the additional electron donor in the presence of S₂O₃ in aqueous solutions, under anaerobic conditions. The main challenge for nZVI application is their tendency to agglomeration, thereby resulting in loss of reactivity that necessitates the use of stabilizers to improve their stability. In this study, S‐nZVI was synthesized by chemical reduction method with starch as a stabilizer. The synthesized nanoparticles were characterized by TEM, XRD, and FTIR. Transmission electron microscopy (TEM) image shows S‐nZVI has a size in the range of 5–27.5 nanometer. Temperature and S‐nZVI concentration were the important factors affecting nitrate removal. Biodenitrification increased at 35°C and 500 mg/L of S‐nZVI, in these conditions, biodenitrification efficiency increased from 40.45 to 78.84%. Experimental results suggested that biodenitrification increased by decreasing initial nitrate concentration. In the bioreactor biodenitrification rate was 94.07% in the presence of S‐nZVI. This study indicated that, Fe²⁺ could be used as the only electron donor or as the additional electron donor in the presence of S₂O₃ to increase denitrification efficiency.     

Study of luminescence properties of dysprosium‐doped CaAl12O19 phosphor for white light‐emitting diodes

Dy³⁺‐doped CaAl₁₂O₁₉ phosphors were synthesized utilizing a combustion method. Crystal structure and morphological examinations were performed respectively using X‐ray diffraction (XRD) and scanning electron microscopy (SEM) techniques to identify the phase and morphology of the synthesized samples. Fourier transform infrared spectroscopy (FTIR) estimations were carried out using the KBr method. Photoluminescence properties (excitation and emission) were recorded at room temperature. CaAl₁₂O₁₉:Dy³⁺ phosphor showed two emission peaks respectively under a 350‐nm excitation wavelength, centered at 477 nm and 573 nm. Dipole–dipole interaction via nonradiative energy shifting has been considered as the major cause of concentration quenching when Dy³⁺ concentration was more than 3 mol%. The CIE chromaticity coordinates positioned at (0.3185, 0.3580) for the CaAl₁₂O₁₉:0.03Dy³⁺ phosphor had a correlated color temperature (CCT) of 6057 K, which is situated in the cool white area. Existing results point out that the CaAl₁₂O₁₉:0.03Dy³⁺ phosphor could be a favorable candidate for use in white light‐emitting diodes (WLEDs).     

A simple and sensitive fluorescence method for the determination of trace ozone in air using acridine red as a probe

The ozone in an air sample was trapped by H₃BO₃‐LK solution to produce iodine (I₂) that interacted with excess I^– to form I₃^–. In pH 4.0 acetate buffer solutions, the I₃^– reacted with acridine red to form acridine red–I₃ ion association particles that resulted in the fluorescence peak decreased at 553 nm. The decreased value ΔF_{553 nm} is linear to the O₃ concentration in the range 0.08–53.3 × 10^–6 mol/L, with a detection limit of 4 × 10^–8 mol/L. This fluorescence method was used to determine ozone in air samples, and the results were in agreement with that of indigo carmine spectrophotometry. Copyright © 2014 John Wiley & Sons, Ltd.     

Inactivation of cholinesterase induced by non-steroidal anti-inflammatory drugs with horseradish peroxidase: Implication for Alzheimer's disease

AimsTo clarify the mechanism of the protective effect of non-steroidal anti-inflammatory drugs (NSAIDs) on Alzheimer's disease, inactivation of cholinesterase (ChE) induced by NSAIDs was examined.Main methodsEquine ChE and rat brain homogenate were incubated with NSAIDs and horseradish peroxidase (HRP) and H₂O₂ (HRP–H₂O₂). ChE activity was measured by using 5,5'-dithiobis(nitrobenzoic acid). By using electron spin resonance, NSAID radicals induced by reaction with HRP–H₂O₂ were detected in the presence of spin trap agents.Key findingsEquine ChE was inactivated by mefenamic acid with HRP–H₂O₂. ChE activity in rat brain homogenate decreased dependent on the concentration of mefenamic acid in the presence of HRP–H₂O₂. NSAIDs diclofenac, indomethacin, phenylbutazone, piroxicam and salicylic acid inactivated ChE. Oxygen radical scavengers did not prevent inactivation of ChE induced by mefenamic acid with HRP–H₂O₂. However, spin trap agents 5,5-dimethyl-1-pyrroline-l-oxide and N-methyl-nitrosopropane, reduced glutathione and ascorbic acid strongly inhibited inactivation of ChE, indicating participation of mefenamic acid radicals. Fluorescent emission of ChE peaked at 400 nm, and the Vmax value of ChE changed during interaction of mefenamic acid with HRP–H₂O₂, indicating that ChE may be inactivated through modification of tyrosine residues by mefenamic radicals.SignificanceThe protective effect of NSAIDs on Alzheimer's disease seems to occur through inactivation of ChE induced by NSAIDs radicals.     

In vivo temperature dependence of cyclic and pseudocyclic electron transport in barley

The effect of temperature on the rate of electron transfer through photosystems I and II (PSI and PSII) was investigated in leaves of barley (Hordeum vulgare L.). Measurements of PSI and PSII photochemistry were made in 21% O₂ and in 2% O₂, to limit electron transport to O₂ in the Mehler reaction. Measurements were made in the presence of saturating CO₂ concentrations to suppress photorespiration. It was observed that the O₂ dependency of PSII electron transport is highly temperature dependent. At 10 °C, the quantum yield of PSII (ΦPSII) was insensitive to O₂ concentration, indicating that there was no Mehler reaction operating. At high temperatures (>25 °C) a substantial reduction in ΦPSII was observed when the O₂ concentration was reduced. However, under the same conditions, there was no effect of O₂ concentration on the ΔpH-dependent process of non-photochemical quenching. The rate of electron transport through PSI was also found to be independent of O₂ concentration across the temperature range. We conclude that the Mehler reaction is not important in maintaining a thylakoid proton gradient that is capable of controlling PSII activity, and present evidence that cyclic electron transport around PSI acts to maintain membrane energisation at low temperature. Received: 6 July 2000 / Accepted: 3 August 2000