Red anemone guild flowers as focal places for mating and feeding by Levant glaphyrid beetles

Several species of glaphyrid (Scarabaeoidea: Glaphyridae) beetles forage and mate on Mediterranean red bowl‐shaped flowers. In red anemones and poppies in Israel, female beetles occupy only a subset of the flowers, do not aggregate, and are hidden below the petals. This raises the question of how males find their mates. In the present study, we investigated the hypothesis that males and females orient to similar plant‐generated cues, thereby increasing their mate encounter prospects. Previous studies have demonstrated that beetle attraction to red models increases with display area. Choice tests with flowers and with models indicate that both male and female beetles prefer large displays. In anemones, beetles rest, feed, and mate mainly on male‐phase flowers, which are larger than female‐phase flowers. Poppies that contain beetles are larger than the population average. These findings support the hypothesis that males and females meet by orienting to large red displays. Corolla size correlates with pollen reward in both plant species, suggesting that visits to large flowers also yield foraging benefits. Male beetles often jump rapidly among adjacent flowers. By contrast to the preference for large flowers by stationary individuals, these jump sequences are random with respect to flower sex‐phase (in anemone) and size (in poppy). They may enable males to detect females at close range. We hypothesize that males employ a mixed mate‐searching strategy, combining orientation to floral signals and to female‐produced cues. The glaphyrids' preference for large flowers may have selected for extraordinarily large displays within the ‘red anemone’ pollination guild of the Levant. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 99 , 808–817.     

C3 plants enhance rates of photosynthesis by reassimilating photorespired and respired CO2

Photosynthetic carbon gain in plants using the C₃ photosynthetic pathway is substantially inhibited by photorespiration in warm environments, particularly in atmospheres with low CO₂ concentrations. Unlike C₄ plants, C₃ 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 C₃ plants rice and wheat employ a specific mechanism to trap and reassimilate photorespired CO₂. 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 CO₂ exiting the cell. This facilitates the capture and reassimilation of photorespired CO₂ in the chloroplast stroma. In both species, 24–38% of photorespired and respired CO₂ were reassimilated within the cell, thereby boosting photosynthesis by 8–11% at ambient atmospheric CO₂ concentration and 17–33% at a CO₂ concentration of 200 µmol mol^?1. Widespread use of this mechanism in tropical and subtropical C₃ plants could explain why the diversity of the world's C₃ flora, and dominance of terrestrial net primary productivity, was maintained during the Pleistocene, when atmospheric CO₂ concentrations fell below 200 µmol mol^?1.     

Temperature response of in vivo Rubisco kinetics and mesophyll conductance in Arabidopsis thaliana: comparisons to Nicotiana tabacum

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 g_m have only been determined in the warm‐adapted Nicotiana tabacum. Here, we measured the temperature response of Rubisco kinetics and g_m in N. tabacum and the cold‐adapted Arabidopsis thaliana using gas exchange and ¹³CO₂ 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, g_m 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 g_m when modelling the temperature response of photosynthesis.     

The acclimation of photosynthesis and respiration to temperature in the C3–C4 intermediate Salsola divaricata: induction of high respiratory CO2 release under low temperature

Photosynthesis in C₃–C₄ intermediates reduces carbon loss by photorespiration through refixing photorespired CO₂ within bundle sheath cells. This is beneficial under warm temperatures where rates of photorespiration are high; however, it is unknown how photosynthesis in C₃–C₄ plants acclimates to growth under cold conditions. Therefore, the cold tolerance of the C₃–C₄ Salsola divaricata was tested to determine whether it reverts to C₃ 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 C₃–C₄ features acclimate to these growth conditions. The CO₂ compensation point and net rates of CO₂ assimilation in cold‐grown plants changed dramatically when measured in response to temperature. However, this was not due to the loss of C₃–C₄ 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.     

The efficiency of C4 photosynthesis under low light conditions in Zea mays,Miscanthus x giganteus and Flaveria bidentis

The efficiency of C₄ photosynthesis in Zea mays, Miscanthus x giganteus and Flaveria bidentis in response to light was determined using measurements of gas exchange, ¹³CO₂ photosynthetic discrimination, metabolite pools and spectroscopic assays, with models of C₄ photosynthesis and leaf ¹³CO₂ discrimination. Spectroscopic and metabolite assays suggested constant energy partitioning between the C₄ and C₃ cycles across photosynthetically active radiation (PAR). Leakiness (φ), modelled using C₄ 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 [CO₂] 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 C₄ cycle and low bundle‐sheath cells CO₂ conductance (g_bs). While F. bidentis had larger g_bs but lower respiration rates and M. giganteus had less C₄ cycle capacity but low g_bs, which resulted in similar φ. This demonstrates that low g_bs is important for efficient C₄ photosynthesis but it is not the only factor determining φ. Additionally, these C₄ species are able to optimize photosynthesis and minimize φ over a range of PARs, including low light.