Handleiding Paprika model “Cultivista” - Project Topmodel4all / 2010-2011

Abstract NL Deze handleiding is bedoeld voor telers die aan de slag willen met het paprika model “Cultivista”. Er wordt uitgelegd hoe met het interactieve paprika model “Cultivista” kan worden gewerkt. De installatie van het model en de verschillende in te voeren gegevens (inputs) van het model worden besproken. Vervolgens worden de werking van het model en de onderdelen van de interface besproken. Tevens worden de voorwaarden voor mogelijke automatisering van de inputs en het oplossen van de meest voorkomende problemen besproken. Abstract UK This manual is meant for growers who would like to work with the sweet pepper growth model “Cultivista”. This manual explains how the model works, how to install the model and which inputs are used. Furthermore, the different parts of the interface are explained. Finally, the conditions for automation of the inputs and troubleshooting of the most common problems are discussed

Het Nieuwe Telen voor groente-opkweek

Het Nieuwe Telen (HNT) is als systeem ontwikkeld voor de primaire productie bedrijven. Voor de opkweekbedrijven, die in korte teelten het basis uitgangsmateriaal maken is dit systeem niet één op één toepasbaar. Om de in Kas als Energiebron opgedane kennis te laten landen bij plantenkwekerijen moet een analyse en een vertaalslag gemaakt worden. In het project ‘Het Nieuwe Telen voor groente-opkweek’ is door middel van gesprekken met 10 opkweekbedrijven, een workshop en literatuurstudie in kaart gebracht waar de kansen en knelpunten liggen

Predicting light-induced stomatal movements based on the redox state of plastoquinone: theory and validation.

Prediction of stomatal conductance is a key element to relate and scale up leaf-level gas exchange processes to canopy, ecosystem and land surface models. The empirical models that are typically employed for this purpose are simple and elegant formulations which relate stomatal conductance on a leaf area basis to the net rate of CO2 assimilation, humidity and CO2 concentration. Although light intensity is not directly modelled as a stomatal opening cue, it is well-known that stomata respond strongly to light. One response mode depends specifically on the blue-light part of the light spectrum, whereas the quantitative or 'red' light response is less spectrally defined and relies more on the quantity of incident light. Here, we present a modification of an empirical stomatal conductance model which explicitly accounts for the stomatal red-light response, based on a mesophyll-derived signal putatively initiated by the chloroplastic plastoquinone redox state. The modified model showed similar prediction accuracy compared to models using a relationship between stomatal conductance and net assimilation rate. However, fitted parameter values with the modified model varied much less across different measurement conditions, lessening the need for frequent re-parameterization to different conditions required of the current model. We also present a simple and easy to parameterize extension to the widely used Farquhar-Von Caemmerer-Berry photosynthesis model to facilitate coupling with the modified stomatal conductance model, which should enable use of the new stomatal conductance model to simulate ecosystem water vapour exchange in terrestrial biosphere models

Drivers of Natural Variation in Water-Use Efficiency Under Fluctuating Light Are Promising Targets for Improvement in Sorghum.

Improving leaf intrinsic water-use efficiency (iWUE), the ratio of photosynthetic CO2 assimilation to stomatal conductance, could decrease crop freshwater consumption. iWUE has primarily been studied under steady-state light, but light in crop stands rapidly fluctuates. Leaf responses to these fluctuations substantially affect overall plant performance. Notably, photosynthesis responds faster than stomata to decreases in light intensity: this desynchronization results in substantial loss of iWUE. Traits that could improve iWUE under fluctuating light, such as faster stomatal movement to better synchronize stomata with photosynthesis, show significant natural diversity in C3 species. However, C4 crops have been less closely investigated. Additionally, while modification of photosynthetic or stomatal traits independent of one another will theoretically have a proportionate effect on iWUE, in reality these traits are inter-dependent. It is unclear how interactions between photosynthesis and stomata affect natural diversity in iWUE, and whether some traits are more tractable drivers to improve iWUE. Here, measurements of photosynthesis, stomatal conductance and iWUE under steady-state and fluctuating light, along with stomatal patterning, were obtained in 18 field-grown accessions of the C4 crop sorghum. These traits showed significant natural diversity but were highly correlated, with important implications for improvement of iWUE. Some features, such as gradual responses of photosynthesis to decreases in light, appeared promising for improvement of iWUE. Other traits showed tradeoffs that negated benefits to iWUE, e.g., accessions with faster stomatal responses to decreases in light, expected to benefit iWUE, also displayed more abrupt losses in photosynthesis, resulting in overall lower iWUE. Genetic engineering might be needed to break these natural tradeoffs and achieve optimal trait combinations, e.g., leaves with fewer, smaller stomata, more sensitive to changes in photosynthesis. Traits describing iWUE at steady-state, and the change in iWUE following decreases in light, were important contributors to overall iWUE under fluctuating light

Improving C4 photosynthesis to increase productivity under optimal and suboptimal conditions.

Although improving photosynthetic efficiency is widely recognized as an underutilized strategy to increase crop yields, research in this area is strongly biased towards species with C3 photosynthesis relative to C4 species. Here, we outline potential strategies for improving C4 photosynthesis to increase yields in crops by reviewing the major bottlenecks limiting the C4 NADP-malic enzyme pathway under optimal and suboptimal conditions. Recent experimental results demonstrate that steady-state C4 photosynthesis under non-stressed conditions can be enhanced by increasing Rubisco content or electron transport capacity, both of which may also stimulate CO2 assimilation at supraoptimal temperatures. Several additional putative bottlenecks for photosynthetic performance under drought, heat, or chilling stress or during photosynthetic induction await further experimental verification. Based on source-sink interactions in maize, sugarcane, and sorghum, alleviating these photosynthetic bottlenecks during establishment and growth of the harvestable parts are likely to improve yield. The expected benefits are also shown to be augmented by the increasing trend in planting density, which increases the impact of photosynthetic source limitation on crop yields

Here comes the sun: How optimization of photosynthetic light reactions can boost crop yields.

Photosynthesis started to evolve some 3.5 billion years ago CO2 is the substrate for photosynthesis and in the past 200-250 years, atmospheric levels have approximately doubled due to human industrial activities. However, this time span is not sufficient for adaptation mechanisms of photosynthesis to be evolutionarily manifested. Steep increases in human population, shortage of arable land and food, and climate change call for actions, now. Thanks to substantial research efforts and advances in the last century, basic knowledge of photosynthetic and primary metabolic processes can now be translated into strategies to optimize photosynthesis to its full potential in order to improve crop yields and food supply for the future. Many different approaches have been proposed in recent years, some of which have already proven successful in different crop species. Here, we summarize recent advances on modifications of the complex network of photosynthetic light reactions. These are the starting point of all biomass production and supply the energy equivalents necessary for downstream processes as well as the oxygen we breathe

Safety conscious or living dangerously: what is the ‘right’ level of plant photoprotection for fitness and productivity?

Due to their sessile nature, plants could be perceived to be relatively slow and rather un-reactive. However, a plant scientist will tell you that the inability to run away (tropism notwithstanding) actually demands a highly sophisticated physiological response to the environment. Light presents an extreme case: cloud cover and wind-induced motion can lead to irradiance changes of several orders of magnitude over timescales of seconds and minutes. Being autotrophic organisms and having evolved to harvest light, plants need to dynamically regulate their biochemistry so that it operates efficiently during these fluxes, maintaining plant fitness but minimising the risk of damage. Photosynthesis is driven at a rate that depends on the amount of available light, as shown by the schematic photosynthesis-light response curves of C3 species (Fig. 1). In nature, CO2 assimilation can go from being light-limited to being light-saturated within a very short period of time. To maximise CO2 uptake, photosynthesis should ‘track’ light levels accurately inducing and removing photoprotective processes accurately. Being able to measure photoprotection precisely in naturally fluctuating settings is difficult; however, a paper in this volume of Plant, Cell and Environment proposes a significant advance (Tietz et al. 2017)

Improving photosynthesis and crop productivity by accelerating recovery from photoprotection

Crop leaves in full sunlight dissipate damaging excess absorbed light energy as heat. When sunlit leaves are shaded by clouds or other leaves, this protective dissipation continues for many minutes and reduces photosynthesis. Calculations have shown that this could cost field crops up to 20% of their potential yield. Here, we describe the bioengineering of an accelerated response to natural shading events in Nicotiana (tobacco), resulting in increased leaf carbon dioxide uptake and plant dry matter productivity by about 15% in fluctuating light. Because the photoprotective mechanism that has been altered is common to all flowering plants and crops, the findings provide proof of concept for a route to obtaining a sustainable increase in productivity for food crops and a much-needed yield jump