Wine vinasses treatments by ozone and an activated sludge system in continuous reactors

In this work wine vinasses have been treated separately by means of a chemical ozonation and a biological aerobic degradation in an activated sludge system, and later by means of a combined process which consisted of an aerobic pretreatment followed by an ozonation treatment, in continuous reactors in all cases. In the ozonation experiments, the hydraulic retention time and the ozone partial pressure were varied leading to substrate removals in the range 4.4-16%, with increases in this removal when both operating variables were increased. A kinetic study, which combines mixed flow reactor model for the liquid phase and plug flow reactor model for the gas phase, allows to determine the rate constant for the ozone reaction and the consumption ratio, which are k_O3 = 3.6 l/(g COD · h) and b = 22.5 g COD degraded/mol O₃ consumed. The aerobic degradation experiments were conducted in the activated sludge system with variations in the retention time and influent organic substrate concentration in the wastewater. A modified Contois model applied to the experimental results leads to the determination of the kinetic parameters of that model: K₁ = 5.43 l/g VSS and q_max = 6.29 g COD/(g VSS · h). Finally, the combined process reveals an improvement in the efficiency of the ozonation stage due to the previous aerobic treatment with increases in the substrate removal reached and in the rate constant obtained, the last one being k_O3 = 5.6 l/(g COD · h).     

Estimation of biological kinetic parameters from an analysis of the BOD curve of waste waters–effects of a chemical preoxidation

Urban waste waters were treated with pure ozone or combinations of ozone, hydrogen peroxide and/or UV radiation to study the course of resulting BOD (biological oxygen demand)-time profiles and to propose a kinetic model. BOD-time profiles of chemically treated waste waters show an initial lag period that first order kinetic models cannot describe. A second order kinetic model is then proposed that satisfactorily fits experimental BOD-time profiles, except when hydrogen peroxide has been used. In these cases, BOD-time profiles present the highest lag periods observed. By applying this model, three parameters are determined: the biokinetic constant (k) which is an index of the biological removal rate; the potential amount of biodegradable matter (BOD_T), and the measure of the size of inocula and microbial activities of microoganisms (λ). The model was checked with experimental results of BOD-time profiles corresponding to both untreated and chemically ozonated urban waste waters. Ozonated waste waters showed the highest values of k and BOD_T, which implies an improvement of waste water biodegradability after ozonation. However, values of λ corresponding to ozonated waste waters presented lower values than those of untreated waste waters. This was due to the lag period observed in the BOD-time profile, which was a consequence of a lack of microorganism acclimation to ozonated waste waters. The effect of the ozone does, pH and carbonates during ozonation on COD (chemical oxygen demand) and the above indicated parameters was also studied. There was an optimum ozone dose which was 138 mg/l for this specific system. This led to the highest biodegradable fraction (φ) and the highest biokinetic constant (39% increase in φ and 4.7- fold increase in the value of k, respectively, compared to untreated waste waters.). Another significant fact was that a higher COD reduction was observed in the absence of carbonate during ozonation at basic pH values. In addition, the percentage of variation in the biodegradable fraction (Δφ) of ozonated waste water increased compared to the untreated waste water at acid pH. The results suggest that ozonolysis, the direct molecular ozone way of reaction, due to its selective character, increases the biodegradability of waste water more than other chemically advanced oxidation processes based on hydroxyl radical reactions.     

Delignification of straw with ozone to enhance biodegradability

Summary Wheat straw was treated with ozone to remove the lignin and increase its biodegradability. The attack of ozone on straw is not selective. Lignin and carbohydrates are oxidized concurrently though the rate of reaction with the latter is slower. A 50% reduction of the original lignin content is optimal for enzymatic hydrolysis. After treatment, 75% of the cellulose in straw is degraded within 24 h as compared to 20% in untreated straw. During ozonation lignin is converted to soluble products which to a great extent are biodegradable and thus yield a useful byproduct. At the moment, ozonation ranks among the more expensive methods of treatment. However, the economics may be improved by reducing the cost of ozone production; this is likely to take place in the near future due to technological improvements, and by reducing the ozone consumption by optimizing the process of ozonation.     

The role of non‐glandular emergences in Croton floribundus (Euphorbiaceae) upon elevated ozone exposures

A role of non‐glandular emergences in avoiding ozone (O₃) damages by preventing its entrance into leaf tissues has been suggested in the O₃‐tolerant species Croton floribundus (Euphorbiaceae). However, this function against O₃ damage has been underestimated due to the covering wax layer, mostly composed of saturated hydrocarbon, which has low O₃ reactivity. To evaluate the role of these emergences in conferring tolerance to O₃, we mechanically removed the non‐glandular emergences from leaf blades of C. floribundus, submitted the plants to acute O₃ fumigation, and assessed morphological and microscopic alterations. Plants with intact leaves treated with O₃ showed the same phenotype as control samples but showed microscopic indicators of accelerated senescence. These alterations indicated a whole‐plant response to O₃. In contrast, plants whose leaves had got their emergences removed exhibited specific morphological symptoms as well as microscopic O₃ damage. We thus conclude that the leaf emergences constitute a barrier for volatile contention, preventing O₃ damage to leaf tissues in C. floribundus. When these structures have been removed, defense volatiles are possibly quickly dispersed, makes this species vulnerable to O₃. This study highlights the relevance of surface structures for plant resistance to O₃ damages, complementing biochemical defenses.     

Tailoring Selectivity of Electrochemical Hydrogen Peroxide Generation by Tunable Pyrrolic‐Nitrogen‐Carbon

The electrochemical reduction of O₂ via a two‐electron reaction pathway to H₂O₂ provides a possibility for replacing the current anthraquinone process, enabling sustainable and decentralized H₂O₂ production. Here, a nitrogen‐rich few‐layered graphene (N‐FLG) with a tunable nitrogen configuration is developed for electrochemical H₂O₂ generation. A positive correlation between the content of pyrrolic‐N and the H₂O₂ selectivity is experimentally observed. The critical role of pyrrolic‐N is elucidated by the variable intermediate adsorption profiles as well as the dependent negative shifts of the pyrrolic‐N peak on X‐ray adsorption near edge structure spectra. By virtue of the optimized N doping configuration and the unique porous structure, the as‐fabricated N‐FLG electrocatalyst exhibits high selectivity toward electrochemical H₂O₂ synthesis as well as superior long‐term stability. To achieve high‐value products on both the anode and cathode with optimized energy efficiency, a practical device coupling electrochemical H₂O₂ generation and furfural oxidation is assembled, simultaneously enabling a high yield rate of H₂O₂ at the cathode (9.66 mol h^?1 g_cat^?1) and 2‐furoic acid at the anode (2.076 mol m^?2 h^?1) under a small cell voltage of 1.8 V.     

Inactivation of Amphidinium sp. in ballast waters using UV/Ag-TiO2+O3 advanced oxidation treatment

Ballast water poses a biological threat to the world’s waterways by transferring aquatic species from one body of water to another. This study investigates the use of combined ultraviolet (UV)/Ag-TiO₂ + ozone (O₃) processes for treating ballast water using Amphidinium sp. as an indicator microorganism. Sufficient Amphidinium sp. cells in ballast waters can be inactivated using O₃ alone, UV irradiation alone (with or without an Ag-TiO₂ coating), and combined treatments. For the low inactivation ratio (<40%) regime, the effects of ozonation and photocatalysis were observed to be cumulative. The combined UV/Ag-TiO₂ + O₃ treatment produced excess hydroxyl radicals and total residual oxidants (TROs), and readily damaged cell membranes to release intracellular substances. The comparison tests revealed that the combined treatments synergistically inactivate Escherichia coli in ballast waters. However, the combined process did not synergistically inactivate Amphidinium sp. cells. Inactivating different aqua species in ballast waters needs distinct treatment methods and dosages.     

EFFECTS OF INCREASING UV‐B RADIATION DUE TO OZONE DEPLETION ON PHOTOSYNTHESIS OF ANTARCTIC CYANOBACTERIA

Ground level ultraviolet‐B (UV‐B; 290–320 nm) fluxes in Antarctica have been increasing due to stratospheric ozone depletion. Although mat‐forming cyanobacteria are major component of freshwater algal biomass in Antarctica, little is known about their response to increasing ultraviolet radiation (UVR). The present study evaluated the sensitivity to UVR of two strains of mat‐forming cyanobacteria with different cell size, Phormidium murrayi (6.0 x 3.2 μm) and Schizothrix calcicola (2.2 x 2.3 μm). Cyanobacterial photosynthesis was measured under different UV spectral quality and quantity achieved by polychromatic filters with different cutoff wavelengths and neutral density screens. The productivity and irradiance data were used to generate biological weighting functions (BWF) for the assessment of UV inhibition on photosynthesis. The kinetics of UV inhibition, as determined by PAM fluorometry, differed between the two species so that inhibition of P. murrayi and S. calcicola were modeled based on UV‐irradiance and cumulative exposure, respectively. After a one hour exposure, BWF's did not differ between the two isolates of cyanobacteria despite their differences in cell size. To evaluate the negative impact of increased UV‐B exposure due to ozone depletion on cyanobacteria, the BWF's were applied to two solar spectra obtained from McMurdo Station, one on a day when the ozone hole was prominent (O₃ = 170 Dobson units; DU = 10‐3 cm O₃), and the other on a day with high ozone concentration (O₃ = 328 DU). The decrease in ozone level would reduce productivity by 3–8%. Seasonal variation of UVR has a bigger impact on cyanobacterial productivity than ozone depletion.     

Ozone‐induced foliar damage and release of stress volatiles is highly dependent on stomatal openness and priming by low‐level ozone exposure in Phaseolus vulgaris

Acute ozone exposure triggers major emissions of volatile organic compounds (VOCs), but quantitatively, it is unclear how different ozone doses alter the start and the total amount of these emissions, and the induction rate of different stress volatiles. It is also unclear whether priming (i.e. pre‐exposure to lower O₃ concentrations) can modify the magnitude and kinetics of volatile emissions. We investigated photosynthetic characteristics and VOC emissions in Phaseolus vulgaris following acute ozone exposure (600 nmol mol^?1 for 30 min) under illumination and in darkness and after priming with 200 nmol mol^?1 O₃ for 30 min. Methanol and lipoxygenase (LOX) pathway product emissions were induced rapidly, followed by moderate emissions of methyl salicylate (MeSA). Stomatal conductance prior to acute exposure was lower in darkness and after low O₃ priming than in light and without priming. After low O₃ priming, no MeSA and lower LOX emissions were detected under acute exposure. Overall, maximum emission rates and the total amount of emitted LOX products and methanol were quantitatively correlated with total stomatal ozone uptake. These results indicate that different stress volatiles scale differently with ozone dose and highlight the key role of stomatal conductance in controlling ozone uptake, leaf injury and volatile release.     

Biomimetic Spider‐Web‐Like Composites for Enhanced Rate Capability and Cycle Life of Lithium Ion Battery Anodes

It is crucial to control the structure and composition of composite anode materials to enhance the cell performance of such anode materials for lithium ion batteries. Herein, a biomimetic strategy is demonstrated for the design of high performance anode materials, inspired by the structural characteristics and working principles of sticky spider‐webs. Hierarchically porous, sticky, spider‐web‐like multiwall carbon nanotube (MWCNT) networks are prepared through a process involving ozonation, ice‐templating assembly, and thermal treatment, thereby integrating the networks with γ‐Fe₂O₃ particles. The spider‐web‐like MWCNT/γ‐Fe₂O₃ composite network not only traps the active γ‐Fe₂O₃ materials tightly but also provides fast charge transport through the 3D internetworked pathways and the mechanical integrity. Consequently, the composite web shows a high capacity of ≈822 mA h g^?1 at 0.05 A g^?1, fast rate capability with ≈72.3% retention at rates from 0.05 to 1 A g^?1, and excellent cycling stability of >88% capacity retention after 310 cycles with a Coulombic efficiency >99%. These remarkable electrochemical performances are attributed to the complementarity of the 3D spider‐web‐like structure with the strong attachment of γ‐Fe₂O₃ particles on the sticky surface. This synthetic strategy offers an environmentally safe, simple, and cost‐effective avenue for the biomimetic design of high performance energy storage materials.     

Effects of elevated O3, alone and in combination with elevated CO2, on tree leaf chemistry and insect herbivore performance: a meta-analysis

We reviewed the effects of elevated ozone (O₃), alone and in combination with elevated carbon dioxide (CO₂) on primary and secondary metabolites of trees and performance of insect herbivores by means of meta‐analysis. Our database consisted of 63 studies conducted on 22 species of trees and published between 1990 and 2005. Ozone alone had no overall effect on concentrations of carbohydrates or nutrients, whereas in combination with CO₂, elevated O₃ reduced nutrient concentrations and increased carbohydrate concentrations. In contrast to primary metabolites, concentrations of phenolics and terpenes were significantly increased by 16% and 8%, respectively, in response to elevated O₃. Effects of ozone in combination with elevated CO₂ were weaker than those of ozone alone on phenolics, but stronger than those of ozone alone on terpenes. The magnitude of secondary metabolite responses depended on the type of ozone exposure facility and increased in the following order: indoor growth chamber 3 than gymnosperms, as shifts in concentrations of carbohydrate and phenolics were observed in the former, but not in the latter. Elevated O₃ had positive effects on some indices of insect performance: pupal mass increased and larval development time shortened, but these effects were counteracted by elevated CO₂. Therefore, despite the observed increase in secondary metabolites, elevated O₃ tends to increase tree foliage quality for herbivores, but elevated CO₂ may alleviate these effects. Our meta‐analysis clearly demonstrated that effects of elevated O₃ alone on leaf chemistry and some indices of insect performance differed from those of O₃+CO₂, and therefore, it is important to study effects of several factors of global climate change simultaneously.     

Iron‐Oxide‐Based Advanced Anode Materials for Lithium‐Ion Batteries

Iron oxides, such as Fe₂O₃ and Fe₃O₄, have recently received increased attention as very promising anode materials for rechargeable lithium‐ion batteries (LIBs) because of their high theoretical capacity, non‐toxicity, low cost, and improved safety. Nanostructure engineering has been demonstrated as an effective approach to improve the electrochemical performance of electrode materials. Here, recent research progress in the rational design and synthesis of diverse iron oxide‐based nanomaterials and their lithium storage performance for LIBs, including 1D nanowires/rods, 2D nanosheets/flakes, 3D porous/hierarchical architectures, various hollow structures, and hybrid nanostructures of iron oxides and carbon (including amorphous carbon, carbon nanotubes, and graphene). By focusing on synthesis strategies for various iron‐oxide‐based nanostructures and the impacts of nanostructuring on their electrochemical performance, novel approaches to the construction of iron‐oxide‐based nanostructures are highlighted and the importance of proper structural and compositional engineering that leads to improved physical/chemical properties of iron oxides for efficient electrochemical energy storage is stressed. Iron‐oxide‐based nanomaterials stand a good chance as negative electrodes for next generation LIBs.     

Water disinfection using the novel approach of ozone and a liquid whistle reactor

A novel approach of ozone treatment assisted by a liquid whistle reactor (LWR), which generates hydrodynamic cavitation, has been explored for water disinfection using a simulated effluent containing Escherichia coli (E. coli), one of the dominant markers in faecal coliforms. A suspension having an E. coli concentration of approximately 10⁸ to 10⁹ CFU mL⁻¹ was introduced into the LWR to examine the effect of hydrodynamic cavitation alone and in combination with ozone. Operating conditions of inlet pressure and ozone doses as well as time of ozonation for individual operation along with the combined operation have been varied with the aim of maximizing the extent of disinfection and arriving at an optimum strategy for treatment. It has been observed that nearly 75% disinfection can be achieved in about 3 h of treatment time using an optimized combination of hydrodynamic cavitation and ozonation. This combination has been found to be a cost-effective technique for achieving maximum disinfection compared to the individual operation of hydrodynamic cavitation (lower extent of disinfection) and ozonation (higher costs of treatment usually due to higher cost of ozone generation).     

Benthic microbial respiration in Appalachian Mountain, Piedmont, and Coastal Plains streams of the eastern U.S.A.

1. Benthic microbial respiration was measured in 214 streams in the Appalachian Mountain, Piedmont, and Coastal Plains regions of the eastern United States in summer 1997 and 1998. 2. Respiration was measured as both O₂ consumption in sealed microcosms and as dehydrogenase activity (DHA) of the sediments contained within the microcosms. 3. Benthic microbial respiration in streams of the eastern U.S., as O₂ consumption, was 0.37 ± 0.03 mg O₂ m^–2 day^–1. Respiration as DHA averaged 1.21 ± 0.08 mg O₂ m^–2 day^–1 4. No significant differences in O₂ consumption or DHA were found among geographical provinces or stream size classes, nor among catchment basins for O₂ consumption, but DHA was significantly higher in the other Atlantic (non‐Chesapeake Bay) catchment basins. 5. Canonical correlation analyses generated two environmental axes. The stronger canonical axis (W₁) represented a chemical disturbance gradient that was negatively correlated with signatures of anthropogenic impacts (ANC, Cl^–, pH, SO₄²), and positively correlated with riparian canopy cover and stream water dissolved organic carbon concentration (DOC). A weaker canonical axis (W₂) was postively correlated with pH, riparian zone agriculture, and stream depth, and negatively correlated with DOC and elevation of the stream. Oxygen consumption was significantly correlated with W₂ whereas DHA was significantly correlated with W₁. 6. The strengths of the correlations of DHA with environmental variables, particularly those that are proven indicators of catchment disturbances and with the canonical axis, suggest that DHA is a more responsive measure of benthic microbial activity than is O₂ consumption.     

Comparison of crop yield sensitivity to ozone between open‐top chamber and free‐air experiments

Assessments of the impacts of ozone (O₃) on regional and global food production are currently based on results from experiments using open‐top chambers (OTCs). However, there are concerns that these impact estimates might be biased due to the environmental artifacts imposed by this enclosure system. In this study, we collated O₃ exposure and yield data for three major crop species—wheat, rice, and soybean—for which O₃ experiments have been conducted with OTCs as well as the ecologically more realistic free‐air O₃ elevation (O₃‐FACE) exposure system; both within the same cultivation region and country. For all three crops, we found that the sensitivity of crop yield to the O₃ metric AOT40 (accumulated hourly O₃ exposure above a cut‐off threshold concentration of 40 ppb) significantly differed between OTC and O₃‐FACE experiments. In wheat and rice, O₃ sensitivity was higher in O₃‐FACE than OTC experiments, while the opposite was the case for soybean. In all three crops, these differences could be linked to factors influencing stomatal conductance (manipulation of water inputs, passive chamber warming, and cultivar differences in gas exchange). Our study thus highlights the importance of accounting for factors that control stomatal O₃ flux when applying experimental data to assess O₃ impacts on crops at large spatial scales.     

Differential responses in two varieties of winter wheat to elevated ozone concentration under fully open‐air field conditions

Two modern cultivars [Yangmai16 (Y16) and Yangfumai 2 (Y2)] of winter wheat (Triticum aestivum L.) with almost identical phenology were investigated to determine the impacts of elevated ozone concentration (E‐O₃) on physiological characters related to photosynthesis under fully open‐air field conditions in China. The plants were exposed from the initiation of tillering to final harvest, with E‐O₃ of 127% of the ambient ozone concentration (A‐O₃). Measurements of pigments, gas exchange rates, chlorophyll a fluorescence and lipid oxidation were made in three replicated plots throughout flag leaf development. In cultivar Y2, E‐O₃ significantly accelerated leaf senescence, as indicated by increased lipid oxidation as well as faster declines in pigment amounts and photosynthetic rates. The lower photosynthetic rates were mainly due to nonstomatal factors, e.g. lower maximum carboxylation capacity, electron transport rates and light energy distribution. In cultivar Y16, by contrast, the effects of E‐O₃ were observed only at the very last stage of flag leaf ageing. Since the two cultivars had almost identical phenology and very similar leaf stomatal conductance before senescence, the greater impacts of E‐O₃ on cultivars Y2 than Y16 cannot be explained by differential ozone uptake. Our findings will be useful for scientists to select O₃‐tolerant wheat cultivars against the rising surface [O₃] in East and South Asia.     

The effect of ozone on the biodegradation of 17α-ethinylestradiol and sulfamethoxazole by mixed bacterial cultures

The potential development of antibacterial resistance and endocrine disruption has led to increased research investigating the removal of contaminants from wastewater (WW) such as sulfamethoxazole (SMX) and 17α-ethinylestradiol (EE2). These compounds react quickly with ozone (O₃), thus ozonation during WW treatment may result in their complete removal. Also, O₃ has demonstrated the ability to increase the biodegradability of WW and certain pharmaceuticals, suggesting its potential as a pretreatment to activated sludge (AS, biological treatment). The objective of this study was to determine whether ozonation, conducted at doses lower than commonly applied to treated WW, would lead to an increased biodegradability of SMX and EE2. The results show that after ozonation performed at lab-scale the bacterial mixtures removed 5 % to 40 % more SMX; however, 2 % to 23 % less EE2 was removed, which was attributed to the observed preferential degradation of a by-product of EE2 ozonation. These results suggest that although ozonation, used as a pretreatment, was shown in literature to increase the overall biodegradability of AS as well as some specific antibiotic compounds and a blood lipid regulator, the potential for increased removal of pharmaceuticals seems to be compound-dependent and cannot yet be extrapolated to this entire class of compounds.     

Nitrogen‐Doped Graphene‐Supported Mixed Transition‐Metal Oxide Porous Particles to Confine Polysulfides for Lithium–Sulfur Batteries

The intricate charge–discharge reactions and bad conductivity nature of sulfur determine the extreme importance of cathode engineering for Li–S batteries. Herein, spinel ZnCo₂O₄ porous particles@N‐doped reduced graphene oxide (ZnCo₂O₄@N‐RGO) are prepared via the combined procedures of refluxing and hydrothermal treatment, consisting of interconnected uniform ZnCo₂O₄ nanocubes with an average size of 5 nm anchored on graphene nanosheets. The as‐obtained composite can act as an inimitable cathode scaffold to suppress the shuttling of polysulfides by chemical confinement of ZnCo₂O₄ and N‐RGO for the first time, as demonstrated by the adsorption energy of ZnCo₂O₄ to Li₂S₄ via the strong chemical bonding between Zn or Co and S. The RGO nanosheets with a relatively high specific surface area provide a good conductive network and structural stability. The introduction of doped N atoms and numerous ZnCo₂O₄ porous nanoparticles can inhibit the transfer of lithium polysulfides between the cathode and anode. Due to the unique structural and compositional features, the as‐obtained hybrid materials with the high sulfur loading of 71% and even 82% still deliver high specific capacity, good rate capability, and enhanced cycling stability with exceptionally high initial Coulombic efficiency, which displays a high utilization of sulfur.     

Recent Advances in Non‐Aqueous Electrolyte for Rechargeable Li–O2 Batteries

The rechargeable Li–O₂ battery has attracted much attention over the past decades owing to its overwhelming advantage in theoretical specific energy density compared to state‐of‐the‐art Li‐ion batteries. Practical application requires non‐aqueous Li–O₂ batteries to stably obtain high reversible capacity, which highly depends on a suitable electrolyte system. Up to now, some critical challenges remain in developing desirable non‐aqueous electrolytes for Li–O₂ batteries. Herein, we will review the current status and challenges in non‐aqueous liquid electrolytes, ionic liquid electrolytes and solid‐state electrolytes of Li–O₂ batteries, as well as the perspectives on these issues and future development.     

Effects of elevated ozone concentration on CH4 and N2O emission from paddy soil under fully open‐air field conditions

We investigated the effects of elevated ozone concentration (E‐O₃) on CH₄ and N₂O emission from paddies with two rice cultivars: an inbred Indica cultivar Yangdao 6 (YD6) and a hybrid one II‐you 084 (IIY084), under fully open‐air field conditions in China. A mean 26.7% enhancement of ozone concentration above the ambient level (A‐O₃) significantly reduced CH₄ emission at tillering and flowering stages leading to a reduction of seasonal integral CH₄ emission by 29.6% on average across the two cultivars. The reduced CH₄ emission is associated with O₃‐induced reduction in the whole‐plant biomass (?13.2%), root biomass (?34.7%), and maximum tiller number (?10.3%), all of which curbed the carbon supply for belowground CH₄ production and its release from submerged soil to atmosphere. Although no significant difference was detected between the cultivars in the CH₄ emission response to E‐O₃, a larger decrease in CH₄ emission with IIY084 (?33.2%) than that with YD6 (?7.0%) was observed at tillering stage, which may be due to the larger reduction in tiller number in IIY084 by E‐O₃. Additionally, E‐O₃ reduced seasonal mean NO_x flux by 5.7% and 11.8% with IIY084 and YD6, respectively, but the effects were not significant statistically. We found that the relative response of CH₄ emission to E‐O₃ was not significantly different from those reported in open‐top chamber experiments. This study has thus confirmed that increasing ozone concentration would mitigate the global warming potential of CH₄ and suggested consideration of the feedback mechanism between ozone and its precursor emission into the projection of future ozone effects on terrestrial ecosystem.     

Elevated ozone concentration decreases whole‐plant hydraulic conductance and disturbs water use regulation in soybean plants

Elevated tropospheric ozone (O₃) concentration has been shown to affect many aspects of plant performance including detrimental effects on leaf photosynthesis and plant growth. However, it is not known whether such changes are accompanied by concomitant responses in plant hydraulic architecture and water relations, which would have great implications for plant growth and survival in face of unfavorable water conditions. A soybean (Glycine max (L.) Merr.) cultivar commonly used in Northeast China was exposed to non‐filtered air (NF, averaged 24.0 nl l^?1) and elevated O₃ concentrations (eO₃, 40 nl l^?1 supplied with NF air) in six open‐top chambers for 50 days. The eO₃ treatment resulted in a significant decrease in whole‐plant hydraulic conductance that is mainly attributable to the reduced hydraulic conductance of the root system and the leaflets, while stem and leaf petiole hydraulic conductance showed no significant response to eO₃. Stomatal conductance of plants grown under eO₃ was lower during mid‐morning but significantly higher at midday, which resulted in substantially more negative daily minimum water potentials. Moreover, excised leaves from the eO₃ treated plants showed significantly higher rates of water loss, suggesting a lower ability to withhold water when water supply is impeded. Our results indicate that, besides the direct detrimental effects of eO₃ on photosynthetic carbon assimilation, its influences on hydraulic architecture and water relations may also negatively affect O₃‐sensitive crops by deteriorating the detrimental effects of unfavorable water conditions.