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Oxygen isotopic composition (Δ18OLW) of leaf water can help improve our understanding of how anatomy interacts with physiology to influence leaf water transport. Leaf water isotope models of Δ18OLW such as the Péclet effect model have been developed to predict Δ18OLW, and it incorporates transpiration rate (E) and the mixing length between unenriched xylem water and enriched mesophyll water, which can occur in the mesophyll (Lm) or veins (Lv). Here we used two cell wall composition mutants grown under two light intensities and RH to evaluate the effect of cell wall composition on Δ18OLW. In maize (Zea mays), the compromised ultrastructure of the suberin lamellae in the bundle sheath of the ALIPHATIC SUBERIN FERULOYL TRANSFERASE mutant (Zmasft) reduced barriers to apoplastic water movement, resulting in higher E and Lv and, consequently, lower Δ18OLW. In cellulose synthase-like F6 (Cslf6) mutants and wildtype of rice (Oryza sativa), the difference in Δ18OLW in plants grown under high and low growth light intensity co-varied with their differences in stomatal density. These results show that cell wall composition and stomatal density influence Δ18OLW by altering the Péclet effect and that stable isotopes can facilitate the development of a physiologically and anatomically explicit water transport model.

Summary: The engineering of C4 photosynthetic activity into the C3 plant rice has the potential to nearly double rice yields. To engineer a two‐cell photosynthetic system in rice, the rice bundle sheath (BS) must be rewired to enhance photosynthetic capacity. Here, we show that BS chloroplast biogenesis is enhanced when the transcriptional activator, Oryza sativa Cytokinin GATA transcription factor 1 (OsCGA1), is driven by a vascular specific promoter. Ectopic expression of OsCGA1 resulted in increased BS chloroplast planar area and increased expression of photosynthesis‐associated nuclear genes (PhANG), required for the biogenesis of photosynthetically active chloroplasts in BS cells of rice. A further refinement using a DNAse dead Cas9 (dCas9) activation module driven by the same cell‐type specific promoter, directed enhanced chloroplast development of the BS cells when gRNA sequences were delivered by the dCas9 module to the promoter of the endogenous OsCGA1 gene. Single gRNA expression was sufficient to mediate the transactivation of both the endogenous gene and a transgenic GUS reporter fused with OsCGA1 promoter. Our results illustrate the potential for tissue‐specific dCas9‐activation and the co‐regulation of genes needed for multistep engineering of C4 rice.

Leaf hydraulic and mesophyll CO2 conductance are both influenced by leaf anatomical traits, however it is poorly understood how the temperature response of these conductances differs between C4 and C3 species with distinct leaf anatomy. This study investigated the temperature response of leaf hydraulic conductance (Kleaf ), stomatal (gs ) and mesophyll (gm ) conductance to CO2 , and leaf anatomical traits in phylogenetically related Panicum antidotale (C4 ) and P. bisulcatum (C3 ) grasses. The C4 species had lower hydraulic conductance outside xylem (Kox ) and Kleaf compared with the C3 species. However, the C4 species had higher gm compared with the C3 species. Traits associated with leaf water movement, Kleaf and Kox , increased with temperature more in the C3 than in the C4 species, whereas traits related to carbon uptake, Anet and gm , increased more with temperature in the C4 than the C3 species. Our findings demonstrate that, in addition to a CO2 concentrating mechanism, outside-xylem leaf anatomy in the C4 species P. antidotale favours lower water movement through the leaf and stomata that provides an additional advantage for greater leaf carbon uptake relative to water loss with increasing leaf temperature than in the C3 species P. bisulcatum.

The high rates of photosynthesis and the carbon concentrating mechanism (CCM) in C4 plants is initiated by the enzyme phosphoenolpyruvate (PEP) carboxylase (PEPC). The flow of inorganic carbon into the CCM of C4 plants is driven by PEPC's affinity for bicarbonate (KHCO3 ), which can be rate limiting when atmospheric CO2 availability is restricted due to low stomatal conductance. We hypothesize that natural variation in KHCO3 across C4 plants is driven by specific amino acid substitutions to impact rates of C4 photosynthesis under environments such as drought that restrict stomatal conductance. To test this hypothesis, we measured KHCO3 from 20 C4 grasses to compare kinetic properties with specific amino acid substitutions. There was nearly a two-fold range in KHCO3 across these C4 grasses (24.3 ± 1.5 to 46.3 ± 2.4 μM), which significantly impacts modeled rates of C4 photosynthesis. Additionally, molecular engineering of a low HCO3 - affinity PEPC identified key domains that confer variation in KHCO3 . This study advances our understanding of PEPC kinetics and builds the foundation for engineering increased HCO3 - affinity and C4 photosynthetic efficiency in important C4 crops.

Breeding economically important C4 crops for enhanced whole-plant water-use efficiency (WUEplant ) is needed for sustainable agriculture. WUEplant is a complex trait and an efficient phenotyping method that reports on components of WUEplant , such as intrinsic water-use efficiency (WUEi , the rate of leaf CO2 assimilation relative to water loss via stomatal conductance), is needed. In C4 plants, theoretical models suggest that leaf carbon isotope composition (δ13 C), when the efficiency of the CO2 -concentrating mechanism (leakiness, ϕ) remains constant, can be used to screen for WUEi . The limited information about how ϕ responds to water limitations confines the application of δ13 C for WUEi screening of C4 crops. The current research aimed to test the response of ϕ to short- or long-term moderate water limitations, and the relationship of δ13 C with WUEi and WUEplant , by addressing potential mesophyll CO2 conductance (gm ) and biochemical limitations in the C4 plant Sorghum bicolor. We demonstrate that gm and ϕ are not responsive to short- or long-term water limitations. Additionally, δ13 C was not correlated with gas-exchange estimates of WUEi under short- and long-term water limitations, but showed a significant negative relationship with WUEplant . The observed association between the δ13 C and WUEplant suggests an intrinsic link of δ13 C with WUEi in this C4 plant, and can potentially be used as a screening tool for WUEplant in sorghum.

In habitats with low water availability, a fundamental challenge for plants will be to maximize photosynthetic C-gain while minimizing transpirational water-loss. This trade-off between C-gain and water-loss can in part be achieved through the coordination of leaf-level photosynthetic and hydraulic traits. To test the relationship of photosynthetic C-gain and transpirational water-loss, we grew, under common growth conditions, 18 C4 grasses adapted to habitats with different mean annual precipitation (MAP) and measured leaf-level structural and anatomical traits associated with mesophyll conductance (gm ) and leaf hydraulic conductance (Kleaf ). The C4 grasses adapted to lower MAP showed greater mesophyll surface area exposed to intercellular air spaces (Smes ) and adaxial stomatal density (SDada ) which supported greater gm . These grasses also showed greater leaf thickness and vein-to-epidermis distance, which may lead to lower Kleaf . Additionally, grasses with greater gm and lower Kleaf also showed greater photosynthetic rates (Anet ) and leaf-level water-use efficiency (WUE). In summary, we identify a suite of leaf-level traits that appear important for adaptation of C4 grasses to habitats with low MAP and may be useful to identify C4 species showing greater Anet and WUE in drier conditions.

Genetic selection for whole-plant water use efficiency (yield per transpiration; WUEplant ) in any crop-breeding programme requires high-throughput phenotyping of component traits of WUEplant such as intrinsic water use efficiency (WUEi ; CO2 assimilation rate per stomatal conductance). Measuring WUEi by gas exchange measurements is laborious and time consuming and may not reflect an integrated WUEi over the life of the leaf. Alternatively, leaf carbon stable isotope composition (δ13 Cleaf ) has been suggested as a potential time-integrated proxy for WUEi that may provide a tool to screen for WUEplant . However, a genetic link between δ13 Cleaf and WUEplant in a C4 species has not been well established. Therefore, to determine if there is a genetic relationship in a C4 plant between δ13 Cleaf and WUEplant under well watered and water-limited growth conditions, a high-throughput phenotyping facility was used to measure WUEplant in a recombinant inbred line (RIL) population created between the C4 grasses Setaria viridis and S. italica. Three quantitative trait loci (QTL) for δ13 Cleaf were found and co-localized with transpiration, biomass accumulation, and WUEplant . Additionally, WUEplant for each of the δ13 Cleaf QTL allele classes was negatively correlated with δ13 Cleaf , as would be predicted when WUEi influences WUEplant . These results demonstrate that δ13 Cleaf is genetically linked to WUEplant , likely to be through their relationship with WUEi , and can be used as a high-throughput proxy to screen for WUEplant in these C4 species.

The conductance of carbon dioxide (CO2 ) from the substomatal cavities to the initial sites of CO2 fixation (gm ) can significantly reduce the availability of CO2 for photosynthesis. There have been many recent reviews on: (i) the importance of gm for accurately modelling net rates of CO2 assimilation, (ii) on how leaf biochemical and anatomical factors influence gm , (iii) the technical limitation of estimating gm , which cannot be directly measured, and (iv) how gm responds to long- and short-term changes in growth and measurement environmental conditions. Therefore, this review will highlight these previous publications but will attempt not to repeat what has already been published. We will instead initially focus on the recent developments on the two-resistance model of gm that describe the potential of photorespiratory and respiratory CO2 released within the mitochondria to diffuse directly into both the chloroplast and the cytosol. Subsequently, we summarize recent developments in the three-dimensional (3-D) reaction-diffusion models and 3-D image analysis that are providing new insights into how the complex structure and organization of the leaf influences gm . Finally, because most of the reviews and literature on gm have traditionally focused on C3 plants we review in the final sections some of the recent developments, current understanding and measurement techniques of gm in C4 and crassulacean acid metabolism (CAM) plants. These plants have both specialized leaf anatomy and either a spatially or temporally separated CO2 concentrating mechanisms (C4 and CAM, respectively) that influence how we interpret and estimate gm compared with a C3 plants.

Mesophyll conductance (gm ) is the diffusion of CO2 from intercellular air spaces (IAS) to the first site of carboxylation in the mesophyll cells. In C3 species, gm is influenced by diverse leaf structural and anatomical traits; however, little is known about traits affecting gm in C4 species. To address this knowledge gap, we used online oxygen isotope discrimination measurements to estimate gm and microscopy techniques to measure leaf structural and anatomical traits potentially related to gm in 18 C4 grasses. In this study, gm scaled positively with photosynthesis and intrinsic water-use efficiency (TEi ), but not with stomatal conductance. Also, gm was not determined by a single trait but was positively correlated with adaxial stomatal densities (SDada ), stomatal ratio (SR), mesophyll surface area exposed to IAS (Smes ) and leaf thickness. However, gm was not related to abaxial stomatal densities (SDaba ) and mesophyll cell wall thickness (TCW ). Our study suggests that greater SDada and SR increased gm by increasing Smes and creating additional parallel pathways for CO2 diffusion inside mesophyll cells. Thus, SDada , SR and Smes are important determinants of C4 -gm and could be the target traits selected or modified for achieving greater gm and TEi in C4 species.

The internal CO2 gradient imposed by mesophyll conductance (gm ) reduces substrate availability for C3 photosynthesis. With several assumptions, estimates of gm can be made from coupled leaf gas exchange with isoflux analysis of carbon ∆13 C-gm and oxygen in CO2 , coupled with transpired water (H2 O) ∆18 O-gm to partition gm into its biochemical and anatomical components. However, these assumptions require validation under changing leaf temperatures. To test these assumptions, we measured and modeled the temperature response (15-40°C) of ∆13 C-gm and ∆18 O-gm along with leaf biochemistry in the C3 grass Panicum bisulcatum, which has naturally low carbonic anhydrase activity. Our study suggests that assumptions regarding the extent of isotopic equilibrium (θ) between CO2 and H2 O at the site of exchange, and that the isotopic composition of the H2 O at the sites of evaporation ( δ w - e 18 ) and at the site of exchange ( δ w - ce 18 ) are similar, may lead to errors in estimating the ∆18 O-gm temperature response. The input parameters for ∆13 C-gm appear to be less sensitive to temperature. However, this needs to be tested in species with diverse carbonic anhydrase activity. Additional information on the temperature dependency of cytosolic and chloroplastic pH may clarify uncertainties used for ∆18 O-gm under changing leaf temperatures.

In C4 photosynthesis, pyruvate orthophosphate dikinase (PPDK) catalyzes the regeneration of phosphoenolpyruvate in the carbon shuttle pathway. Although the biochemical function of PPDK in maize is well characterized, a genetic analysis of PPDK has not been reported. In this study, we use the maize transposable elements Mutator and Ds to generate multiple mutant alleles of PPDK. Loss-of-function mutants are seedling lethal, even when plants were grown under 2% CO2 , and they show very low capacity for CO2 assimilation, indicating C4 photosynthesis is essential in maize. Using RNA-seq and GC-MS technologies, we examined the transcriptional and metabolic responses to a deficiency in PPDK activity. These results indicate loss of PPDK results in downregulation of gene expression of enzymes of the C4 cycle, the Calvin cycle, and components of photochemistry. Furthermore, the loss of PPDK did not change Kranz anatomy, indicating that this metabolic defect in the C4 cycle did not impinge on the morphological differentiation of C4 characters. However, sugar metabolism and nitrogen utilization were altered in the mutants. An interaction between light intensity and genotype was also detected from transcriptome profiling, suggesting altered transcriptional and metabolic responses to environmental and endogenous signals in the PPDK mutants.

Diffusion of CO2 from the leaf intercellular air space to the site of carboxylation (gm ) is a potential trait for increasing net rates of CO2 assimilation (Anet ), photosynthetic efficiency, and crop productivity. Leaf anatomy plays a key role in this process; however, there are few investigations into how cell wall properties impact gm and Anet . Online carbon isotope discrimination was used to determine gm and Anet in Oryza sativa wild-type (WT) plants and mutants with disruptions in cell wall mixed-linkage glucan (MLG) production (CslF6 knockouts) under high- and low-light growth conditions. Cell wall thickness (Tcw ), surface area of chloroplast exposed to intercellular air spaces (Sc ), leaf dry mass per area (LMA), effective porosity, and other leaf anatomical traits were also analyzed. The gm of CslF6 mutants decreased by 83% relative to the WT, with c. 28% of the reduction in gm explained by Sc . Although Anet /LMA and Anet /Chl partially explained differences in Anet between genotypes, the change in cell wall properties influenced the diffusivity and availability of CO2 . The data presented here indicate that the loss of MLG in CslF6 plants had an impact on gm and demonstrate the importance of cell wall effective porosity and liquid path length on gm .

Mesophyll conductance (gm ) describes the movement of CO2 from the intercellular air spaces below the stomata to the site of initial carboxylation in the mesophyll. In contrast with C3 -gm , little is currently known about the intraspecific variation in C4 -gm or its responsiveness to environmental stimuli. To address these questions, gm was measured on five maize (Zea mays) lines in response to CO2 , employing three different estimates of gm . Each of the methods indicated a significant response of gm to CO2 . Estimates of gm were similar between methods at ambient and higher CO2 , but diverged significantly at low partial pressures of CO2 . These differences are probably driven by incomplete chemical and isotopic equilibrium between CO2 and bicarbonate under these conditions. Carbonic anhydrase and phosphoenolpyruvate carboxylase in vitro activity varied significantly despite similar values of gm and leaf anatomical traits. These results provide strong support for a CO2 response of gm in Z. mays, and indicate that gm in maize is probably driven by anatomical constraints rather than by biochemical limitations. The CO2 response of gm indicates a potential role for facilitated diffusion in C4 -gm . These results also suggest that water-use efficiency could be enhanced in C4 species by targeting gm .

Summary The group of homoiochlorophyllous resurrection plants evolved the unique capability to survive severe drought stress without dismantling the photosynthetic machinery. This implies that they developed efficient strategies to protect the leaves from reactive oxygen species (ROS) generated by photosynthetic side reactions. These strategies, however, are poorly understood. Here, we performed a detailed study of the photosynthetic machinery in the homoiochlorophyllous resurrection plant Craterostigma pumilum during dehydration and upon recovery from desiccation. During dehydration and rehydration, C. pumilum deactivates and activates partial components of the photosynthetic machinery in a specific order, allowing for coordinated shutdown and subsequent reinstatement of photosynthesis. Early responses to dehydration are the closure of stomata and activation of electron transfer to oxygen accompanied by inactivation of the cytochrome b6f complex leading to attenuation of the photosynthetic linear electron flux (LEF). The decline in LEF is paralleled by a gradual increase in cyclic electron transport to maintain ATP production. At low water contents, inactivation and supramolecular reorganization of photosystem II becomes apparent, accompanied by functional detachment of light-harvesting complexes and interrupted access to plastoquinone. This well-ordered sequence of alterations in the photosynthetic thylakoid membranes helps prepare the plant for the desiccated state and minimize ROS production.

Photosynthesis in C(3) -C(4) intermediates reduces carbon loss by photorespiration through refixing photorespired CO(2) within bundle sheath cells. This is beneficial under warm temperatures where rates of photorespiration are high; however, it is unknown how photosynthesis in C(3) -C(4) plants acclimates to growth under cold conditions. Therefore, the cold tolerance of the C(3) -C(4) Salsola divaricata was tested to determine whether it reverts to C(3) photosynthesis when grown under low temperatures. Plants were grown under cold (15/10 °C), moderate (25/18 °C) or hot (35/25 °C) day/night temperatures and analysed to determine how photosynthesis, respiration and C(3) -C(4) features acclimate to these growth conditions. The CO(2) compensation point and net rates of CO(2) assimilation in cold-grown plants changed dramatically when measured in response to temperature. However, this was not due to the loss of C(3) -C(4) intermediacy, but rather to a large increase in mitochondrial respiration supported primarily by the non-phosphorylating alternative oxidative pathway (AOP) and, to a lesser degree, the cytochrome oxidative pathway (COP). The increase in respiration and AOP capacity in cold-grown plants likely protects against reactive oxygen species (ROS) in mitochondria and photodamage in chloroplasts by consuming excess reductant via the alternative mitochondrial respiratory electron transport chain.

Traditionally, it was believed that C(4) photosynthesis required two types of chlorenchyma cells to concentrate CO(2) within the leaf. However, several species have been identified that perform C(4) photosynthesis using dimorphic chloroplasts within an individual cell. The goal of this research was to determine how growth under limited light affects leaf structure, biochemistry and efficiency of the single-cell CO(2) -concentrating mechanism in Bienertia sinuspersici. Measurements of rates of CO(2) assimilation and CO(2) isotope exchange in response to light intensity and O(2) were used to determine the efficiency of the CO(2) -concentrating mechanism in plants grown under moderate and low light. In addition, enzyme assays, chlorophyll content and light microscopy of leaves were used to characterize acclimation to light-limited growth conditions. There was acclimation to growth under low light with a decrease in capacity for photosynthesis when exposed to high light. This was associated with a decreased investment in biochemistry for carbon assimilation with only subtle changes in leaf structure and anatomy. The capture and assimilation of CO(2) delivered by the C(4) cycle was lower in low-light-grown plants. Low-light-grown plants were able to acclimate to maintain structural and functional features for the performance of efficient single-cell C(4) photosynthesis.

Biochemical models are used to predict and understand the response of photosynthesis to rising temperatures and CO2 partial pressures. These models require the temperature dependency of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) kinetics and mesophyll conductance to CO2 (g(m)). However, it is not known how the temperature response of Rubisco kinetics differs between species, and comprehensive in vivo Rubisco kinetics that include gm have only been determined in the warm-adapted Nicotiana tabacum. Here, we measured the temperature response of Rubisco kinetics and gm in N. tabacum and the cold-adapted Arabidopsis thaliana using gas exchange and (13)CO2 isotopic discrimination on plants with genetically reduced levels of Rubisco. While the individual Rubisco kinetic parameters in N. tabacum and A. thaliana were similar across temperatures, they collectively resulted in significantly different modelled rates of photosynthesis. Additionally, gm increased with temperature in N. tabacum but not in A. thaliana. These findings highlight the importance of considering species-dependent differences in Rubisco kinetics and gm when modelling the temperature response of photosynthesis.

The efficiency of C(4) photosynthesis in Zea mays, Miscanthus x giganteus and Flaveria bidentis in response to light was determined using measurements of gas exchange, (13) CO(2) photosynthetic discrimination, metabolite pools and spectroscopic assays, with models of C(4) photosynthesis and leaf (13) CO(2) discrimination. Spectroscopic and metabolite assays suggested constant energy partitioning between the C(4) and C(3) cycles across photosynthetically active radiation (PAR). Leakiness (φ), modelled using C(4) light-limited photosynthesis equations (φ(mod)), matched values from the isotope method without simplifications (φ(is)) and increased slightly from high to low PAR in all species. However, simplifications of bundle-sheath [CO(2)] and respiratory fractionation lead to large overestimations of φ at low PAR with the isotope method. These species used different strategies to maintain similar φ. For example, Z. mays had large rates of the C(4) cycle and low bundle-sheath cells CO(2 ) conductance (g(bs)). While F. bidentis had larger g(bs) but lower respiration rates and M. giganteus had less C(4) cycle capacity but low g(bs), which resulted in similar φ. This demonstrates that low g(bs) is important for efficient C(4) photosynthesis but it is not the only factor determining φ. Additionally, these C(4) species are able to optimize photosynthesis and minimize φ over a range of PARs, including low light.

Photosynthetic carbon gain in plants using the C(3) photosynthetic pathway is substantially inhibited by photorespiration in warm environments, particularly in atmospheres with low CO(2) concentrations. Unlike C(4) plants, C(3) plants are thought to lack any mechanism to compensate for the loss of photosynthetic productivity caused by photorespiration. Here, for the first time, we demonstrate that the C(3) plants rice and wheat employ a specific mechanism to trap and reassimilate photorespired CO(2) . A continuous layer of chloroplasts covering the portion of the mesophyll cell periphery that is exposed to the intercellular air space creates a diffusion barrier for CO(2) exiting the cell. This facilitates the capture and reassimilation of photorespired CO(2) in the chloroplast stroma. In both species, 24-38% of photorespired and respired CO(2) were reassimilated within the cell, thereby boosting photosynthesis by 8-11% at ambient atmospheric CO(2) concentration and 17-33% at a CO(2) concentration of 200 µmol mol(-1) . Widespread use of this mechanism in tropical and subtropical C(3) plants could explain why the diversity of the world's C(3) flora, and dominance of terrestrial net primary productivity, was maintained during the Pleistocene, when atmospheric CO(2) concentrations fell below 200 µmol mol(-1) .

The CO2 concentration in Earth's atmosphere may double during this century. Plant responses to such an increase depend strongly on their nitrogen status, but the reasons have been uncertain. Here, we assessed shoot nitrate assimilation into amino acids via the shift in shoot CO2 and O2 fluxes when plants received nitrate instead of ammonium as a nitrogen source (deltaAQ). Shoot nitrate assimilation became negligible with increasing CO2 in a taxonomically diverse group of eight C3 plant species, was relatively insensitive to CO2 in three C4 species, and showed an intermediate sensitivity in two C3-C4 intermediate species. We then examined the influence of CO2 level and ammonium vs. nitrate nutrition on growth, assessed in terms of changes in fresh mass, of several C3 species and a Crassulacean acid metabolism (CAM) species. Elevated CO2 (720 micromol CO2/mol of all gases present) stimulated growth or had no effect in the five C3 species tested when they received ammonium as a nitrogen source but inhibited growth or had no effect if they received nitrate. Under nitrate, two C3 species grew faster at sub-ambient (approximately 310 micromol/mol) than elevated CO2. A CAM species grew faster at ambient than elevated or sub-ambient CO2 under either ammonium or nitrate nutrition. This study establishes that CO2 enrichment inhibits shoot nitrate assimilation in a wide variety of C3 plants and that this phenomenon can have a profound effect on their growth. This indicates that shoot nitrate assimilation provides an important contribution to the nitrate assimilation of an entire C3 plant. Thus, rising CO2 and its effects on shoot nitrate assimilation may influence the distribution of C3 plant species.

Differences in light quality penetration within a leaf and absorption by the photosystems alter rates of CO2 assimilation in C3 plants. It is also expected that light quality will have a profound impact on C4 photosynthesis due to disrupted coordination of the C4 and C3 cycles. To test this hypothesis, we measured leaf gas exchange, 13CO2 discrimination (Δ13C), photosynthetic metabolite pools and Rubisco activation state in Zea mays and Miscanthus × giganteus under steady-state red, green, blue and white light. Photosynthetic rates, quantum yield of CO2 assimilation, and maximum phosphoenolpyruvate carboxylase activity were significantly lower under blue light than white, red and green light in both species. However, similar leakiness under all light treatments suggests the C4 and C3 cycles were coordinated to maintain the photosynthetic efficiency. Measurements of photosynthetic metabolite pools also suggest coordination of C4 and C3 cycles across light treatments. The energy limitation under blue light affected both C4 and C3 cycles, as we observed a reduction in C4 pumping of CO2 into bundle-sheath cells and a limitation in the conversion of C3 metabolite phosphoglycerate to triose phosphate. Overall, light quality affects rates of CO2 assimilation, but not the efficiency of CO2 concentrating mechanism.

The photosynthetic efficiency of the CO(2)-concentrating mechanism in two forms of single-cell C(4) photosynthesis in the family Chenopodiaceae was characterized. The Bienertioid-type single-cell C(4) uses peripheral and central cytoplasmic compartments (Bienertia sinuspersici), while the Borszczowioid single-cell C(4) uses distal and proximal compartments of the cell (Suaeda aralocaspica). C(4) photosynthesis within a single-cell raises questions about the efficiency of this type of CO(2) -concentrating mechanism compared with the Kranz-type. We used measurements of leaf CO(2) isotope exchange (Δ(13) C) to compare the efficiency of the single-cell and Kranz-type forms of C(4) photosynthesis under various temperature and light conditions. Comparisons were made between the single-cell C(4) and a sister Kranz form, S. eltonica[NAD malic enzyme (NAD ME) type], and with Flaveria bidentis[NADP malic enzyme (NADP-ME) type with Kranz Atriplicoid anatomy]. There were similar levels of Δ(13) C discrimination and CO(2) leakiness (Φ) in the single-cell species compared with the Kranz-type. Increasing leaf temperature (25 to 30 °C) and light intensity caused a decrease in Δ(13) C and Φ across all C(4) types. Notably, B. sinuspersici had higher Δ(13) C and Φ than S. aralocaspica under lower light. These results demonstrate that rates of photosynthesis and efficiency of the CO(2) -concentrating mechanisms in single-cell C(4) plants are similar to those in Kranz-type.

Carbon and oxygen isotope discrimination of CO(2) during photosynthesis (Δ(13)C(obs) and Δ(18)O(obs)) were measured along a monocot leaf, triticale (Triticum × Secale). Both Δ(13)C(obs) and Δ(18)O(obs) increased towards the leaf tip. While this was expected for Δ(18)O(obs) , because of progressive enrichment of leaf water associated with the Peclet effect, the result was surprising for Δ(13) C(obs). To explore parameters determining this pattern, we measured activities of key photosynthetic enzymes [ribulose bis-phosphate carboxylase-oxygenase (Rubisco), phosphoenolpyruvate carboxylase (PEPC) and carbonic anhydrase) as well as maximum carboxylation and electron transport rates (V(cmax) and J(max)) along the leaf. Patterns in leaf internal anatomy along the leaf were also quantified. Mesophyll conductance (g(m)) is known to have a strong influence on Δ(13)C(obs) , so we used three commonly used estimation methods to quantify variation in g(m) along the leaf. Variation in Δ(13)C(obs) was correlated with g(m) and chloroplast surface area facing the intercellular air space, but unrelated to photosynthetic enzyme activity. The observed variation could cause errors at higher scales if the appropriate portion of a leaf is not chosen for leaf-level measurements and model parameterization. Our study shows that one-third of the way from the base of the leaf represents the most appropriate portion to enclose in the leaf chamber.

Measurements of net fluxes of CO2 and O2 from leaves and chlorophyll a fluorescence were used to determine the role of mitochondrial respiration during nitrate (NO3–) assimilation in both a C3 (wheat) and a C4 (maize) plant. Changes in the assimilatory quotient (net CO2 consumed over net O2 evolved) when the nitrogen source was shifted from NO3– to NH4+ (ΔAQ) provided a measure of shoot NO3– assimilation. According to this measure, elevated CO2 inhibited NO3– assimilation in wheat but not maize. Net O2 exchange under ambient CO2 concentrations increased in wheat plants receiving NO3– instead of NH4+, but gross O2 evolution from the photosynthetic apparatus (JO2) was insensitive to nitrogen source. Therefore, O2 consumption within wheat photosynthetic tissue (ΔΟ2), the difference between JO2 and net O2 exchange, decreased during NO3– assimilation. In maize, NO3– assimilation was insensitive to changes in intercellular CO2 concentration (Ci); nonetheless, ΔΟ2 at low Ci values was significantly higher in NO3–-fed than in NH4+-fed plants. Changes in O2 consumption during NO3– assimilation may involve one or more of the following processes: (a) Mehler ascorbate peroxidase (MAP) reactions; (b) photorespiration; or (c) mitochondrial respiration. The data presented here indicates that in wheat, the last process, mitochondrial respiration, is decreased during NO3– assimilation. In maize, NO3– assimilation appears to stimulate mitochondrial respiration when photosynthetic rates are limiting.

Measurements of CO 2 and O 2 gas exchange and chlorophyll a fluorescence were used to test the hypothesis that elevated atmospheric CO 2 inhibits nitrate (NO 3 ‐ ) photo-assimilation in the C 4 plant, maize ( Zea mays L.). The assimilatory quotient ( AQ ), the ratio of net CO 2 assimilation to net O 2 evolution, decreases as NO 3 ‐ photo-assimilation increases so that the difference in AQ between the ammonium- and nitrate-fed plants ( D D D AQ ) provided an in planta estimate of NO 3 ‐ photo-assimilation. In fully expanded maize leaves, NO 3 ‐ photo-assimilation was detectable only under high light and was not affected by CO 2 treatments. Furthermore, CO 2 assimilation and O 2 evolution were higher under NO 3 ‐ than ammonia (NH 4 + + + ) regardless of CO 2 levels. In conclusion, NO 3 ‐ photo-assimilation in maize primarily occurred at high light when reducing equivalents were presumably not limiting. Nitrate photo-assimilation enhanced C 4 photosynthesis, and in contrast to C 3 plants, elevated CO 2 did not inhibit foliar NO 3 ‐ photo-assimilation.

The present study was carried out to test the hypothesis that elevated atmospheric CO 2 (Ca) will alleviate over-excitation of the C 4 photosynthetic apparatus and decrease non-photochemical quenching (NPQ) during periods of limited water availability. Chlorophyll a fluorescence was monitored in Sorghum bicolor plants grown under a freeair carbon-dioxide enrichment (FACE) by water-stress (Dry) experiment. Under Dry conditions elevated Ca increased the quantum yield of photosystem II ( f PSII) throughout the day through increases in both photochemical quenching coefficient ( q p ) and the efficiency with which absorbed quanta are transferred to open PSII reaction centres ( F v ¢¢¢ ¢ / F m ¢¢ ). However, in the well-watered plants (Wets) FACE enhanced f PSII only at midday and was entirely attributed to changes in F v ¢¢¢ ¢ / F m ¢¢ . Under field conditions, decreases in f f f PSII under Dry treatments and ambient Ca corresponded to increases in NPQ but the de-epoxidation state of the xanthophyll pool (DPS) showed no effects. Water-stress did not lead to long-term damage to the photosynthetic apparatus as indicated by f PSII and carbon assimilation measured after removal of stress conditions. We conclude that elevated Ca enhances photochemical light energy usage in C 4 photosynthesis during drought and/ or midday conditions. Additionally, NPQ protects against photo-inhibition and photodamage. However, NPQ and the xanthophyll cycle were affected differently by elevated Ca and water-stress.

○ The interactive effects of atmospheric CO 2 concentration and soil-water content on grain sorghum (Sorghum bicolor) are reported here. ○ Sorghum plants were exposed to ambient (control) and free-air CO 2 enrichment (FACE; ambient + 200 μmol mol -1 ), under ample (wet, 100% replacement of evapotranspiration) and reduced (dry, postplanting and mid-season irrigations) water supply over two growing seasons. ○ FACE reduced seasonal average stomatal conductance (g s ) by 0.17 mol (H 2 O) m -2 s -1 (32% and 37% for dry and wet, respectively) compared with control; this was similar to the difference between dry and wet treatments. FACE increased net assimilation rate (A) by 4.77 μmol (CO 2 ) m -2 s -1 (23% and 9% for dry and wet, respectively), whereas dry decreased A by 10.50 μmol (CO 2 ) m -2 s -1 (26%) compared with wet. Total plant water potential (ψ w ) was 0.16 MPa (9%) and 0.04 MPa (3%) less negative in FACE than in the control treatment for dry and wet, respectively. Under dry, FACE stimulated final shoot biomass by 15%. ○ By ameliorating the adverse effects of drought, elevated atmospheric CO 2 improved plant water status, which indirectly caused an increase in carbon gain.

Summary • Sorghum (Sorghum bicolor) was grown for two consecutive seasons at Maricopa, AZ, USA, using the free-air CO2 enrichment (FACE) approach to investigate evapotranspiration of this C4 plant at ample and limited water supplies. • Crop evapotranspiration (ET) was measured using two CO2 concentrations (control, c. 370 µmol mol−1; FACE, ambient +200 µmol mol−1) and two irrigation treatments (well watered and water-limited). Volumetric soil water content was measured before and after each irrigation using neutron scattering techniques. • Averaged over both years, elevated CO2 reduced cumulative ET by 10% when plants were given ample water and by 4% under severe drought stress. Water-use efficiency based on grain yield (WUE-G) increased, due to CO2 enrichment, by 9% and 19% in wet and dry plots, respectively; based on total biomass, water-use efficiency (WUE-B) increased by 16% and 17% in wet and dry plots, respectively. • These data suggest that in the future high-CO2 environment, water requirements for irrigated sorghum will be lower than at present, while dry-land productivity will increase, provided global warming is minimal.

Summary • To determine the response of C4 plants to elevated CO2 it is necessary to establish whether young leaves have a fully developed C4 photosynthetic apparatus, and whether photosynthesis in these leaves is responsive to elevated CO2. • The effect of free-air CO2 enrichment (FACE) on the photosynthetic development of the C4 crop Sorghum bicolor was monitored. Simultaneous measurements of chlorophyll a fluorescence and carbon assimilation were made to determine energy utilization, quantum yields of carbon fixation (φCO2) and photosystem II (φPSII), as well as photorespiration. • Assimilation in the second leaf of FACE plants was 37% higher than in control plants and lower apparent rates of photorespiration at growth CO2 concentrations were exhibited. In these leaves, φPSII : φCO2 was high at low atmospheric CO2 concentration (Ca) due to overcycling of the C4 pump and increased leakiness. As Ca increased, φPSII : φCO2 decreased as a greater proportion of energy derived from linear electron transfer was used by the C3 cycle. • The stimulation of C4 photosynthesis at elevated Ca in young leaves was partially due to suppressed photorespiration. Additionally, elevated Ca enhanced energy-use efficiency in young leaves, possibly by decreasing CO2 leakage from bundle sheath cells, and by decreasing overcycling of the C4 pump.

In many bioartificial liver systems currently being designed and evaluated for use in fulminant hepatic failure, direct contact is required between the patient's blood and the liver cells in the device. The efficacy of such devices will be influenced by the interaction of fulminant hepatic failure (FHF) patient serum with the cells. We have found that FHF serum inhibits the growth rate and the synthesis of DNA, RNA, and protein; disturbs glutathione homeostasis; and induces morphological changes in cultured human Hep G2 cells. These interactions should influence the design of bioartificial liver devices based on proliferating cell lines and indicate the requirement to pretreat FHF patient plasma to reduce the toxin load.

There has been increasing interest in the development of a hepatocyte bioreactor for the treatment of acute hepatic failure; however, little is known about the effect of hepatocyte byproducts on the viability of the cells in the bioreactor environment. We investigated the effects of increasing concentrations of bile on the growth and viability of the human hepatoma cell line Hep G2 and on the cytochrome P-450 content and dependent mixed function oxidase (MFO) activities, reduced glutathione (GSH) content, and glutathione S-transferase (GST) activity of primary cultures of rat hepatocytes. Our purpose was to determine whether or not it would be necessary to pretreat the plasma from patients with acute liver failure to remove elevated bile concentrations which might be toxic to the hepatocytes in an artificial liver device. Bile was found to inhibit Hep G2 cell growth at concentrations as low as 0.1% and to decrease viability at concentrations above 0.5%. The cytochrome P-450 and GSH contents and the activities of the MFO system and of GST were decreased in the primary cultures of hepatocytes following 24 h treatment with concentrations of bile at and above 0.5%. The MFO activities associated with different cytochrome P-450 isoenzymes decreased to different extents in the presence of bile with the O-dealkylation of pentoxyresorufin being more labile than that of ethoxyresorufin. Our data indicate that elevated bile concentrations are cytotoxic to liver cells, and it may be necessary to pretreat patient plasma to decrease its bile content to protect the cells during the clinical operation of a hepatocyte bioreactor device.

Much effort has been directed toward the development of serum-free, hormonally defined culture conditions for the maintenance of differentiated functions in many cell types, including hepatocytes. However, in the development of a hepatocyte bioreactor for artificial liver support, many designs propose the maintenance of cells in plasma as opposed to defined culture medium. There is very little reported literature on the growth and function of cells cultured in plasma or serum; therefore, the effect of increasing serum concentrations was investigated using the human hepatoma, Hep G2, as a model cell line. It was found that Hep G2 can survive and grow in 100% serum if the serum is supplemented with L-glutamic acid, glycine, and L-cysteine.

Features characteristic of hypertext are no longer the providence of specialized hypertext systems. Interfaces exhibiting the “power of linking” can be found in software ranging from document preparation programs to operating systems, providing users with many new ap proaches to individual and group information management. To take advantage of the new opportunities afforded by this migration, it is important to understand hypertext at representation levels beneath the more superficial aspects of the human-computer interface. Three abstract models for hypertext-representative members of a spectrum of popular formalisms-are presented to provide insight into the meaning and potential of hypertext. Each model represents a different level in the design-decision process necessary for effective hypertext development, and each model plays an important role in development and use of information management software exhibiting hypertext features. Hypertext provides new methods for organizing and presenting information. The technology has been employed to facilitate personal information management, improve use of large information resources, and coordinate complex planning tasks. Support for hypertexts and related systems is motivated by a belief that hypertext can provide more efficient and personalized access to text by complementing the global search techniques of traditional information retrieval systems with focal navigation based on meaningful inter- and intradocument connections or “links” identified by other means. Informally, hypertext is simply a collection of modular text elements and a set of inter- and intraelement relationships that can be ordered in many ways and used to satisfy a broad range of personalized information needs. More formally, hypertext is: (1) a database of text; (2) a semantic net which connects text components; and (3) tools for creating and manipulating this combination of text and semantic net (Conklin, 1987; Rada & Lunin, 1989; Schnase, Leggett, Kacmar, & Boyle, 1988). Hypermedia is hypertext with nontextual elements. Software is said to possess “hypertext func

Examined the factor structure, construct validity, and reliability of the SONG and the PIL in a sample of 248 introductory psychology students. Ten interpretable independent dimensions of satisfaction with life were extracted, with 6 factors that loaded on the PIL and 4 that loaded on the SONG. These data support Crumbaugh's (1977) assertion that the SONG is a complementary scale to the PIL contributing factors that deal with the strength of motivation to find meaning and purpose in life. In addition, the SONG and the PIL were shown to be highly reliable and valid instruments. Further research that uses SONG-PIL factor scores and profile analysis is recommended.