118 research outputs found
Resource use efficiency of indoor lettuce (Lactuca sativa L.) cultivation as affected by red:blue ratio provided by LED lighting
LED lighting in indoor farming systems allows to modulate the spectrum to fit plant needs. Red (R) and blue (B) lights are often used, being highly active for photosynthesis. The effect of R and B spectral components on lettuce plant physiology and biochemistry and resource use efficiency were studied. Five red:blue (RB) ratios (0.5-1-2-3-4) supplied by LED and a fluorescent control (RB = 1) were tested in six experiments in controlled conditions (PPFD = 215 μmol m-2 s-1, daylength 16 h). LED lighting increased yield (1.6 folds) and energy use efficiency (2.8 folds) as compared with fluorescent lamps. Adoption of RB = 3 maximised yield (by 2 folds as compared with RB = 0.5), also increasing leaf chlorophyll and flavonoids concentrations and the uptake of nitrogen, phosphorus, potassium and magnesium. As the red portion of the spectrum increased, photosystem II quantum efficiency decreased but transpiration decreased more rapidly, resulting in increased water use efficiency up to RB = 3 (75 g FW L-1 H2O). The transpiration decrease was accompanied by lower stomatal conductance, which was associated to lower stomatal density, despite an increased stomatal size. Both energy and land surface use efficiency were highest at RB ≥ 3. We hereby suggest a RB ratio of 3 for sustainable indoor lettuce cultivation
Data from: Energy savings in greenhouses by transition from high-pressure sodium to LED lighting
These simulations describe the dynamic changes (5 minute intervals) of the indoor climate (temperature, humidity, CO2 concentration) and energy consumption (lighting and heating) of a simulated greenhouse season in a typical meteorological year (350 days starting September 27). A modern, Venlo type, 4 hectare greenhouse with a tomato crop is simulated, with either HPS or LED lamps. 15 different weather scenarios from around the world are included, as well as various settings for design and climate control. The GreenLight model, https://github.com/davkat1/GreenLight, was used for this purpose
Differential effect of transpiration and Ca supply on growth and Ca concentration of tomato plants
To determine the extent to which transpiration and Ca concentration in the nutrient solution affect the regulation of growth, two independent experiments with young tomato plants were carried out under fully controlled climate conditions and grown hydroponically. The first experiment consisted of the regulation of transpiration by three levels of relative air humidity (RH): 50%, 70% (control) and 95% (corresponding to 1.32, 0.79 and 0.13 kPa, respectively) during 7 days. The second experiment involved four periods of 1, 3, 7 or 14 days of low-calcium (0.5 meq L¿1) compared with the nutrient standard solution (9 meq L¿1). The results show that plant growth was affected more by RH than by the reduction of Ca in the nutrient solution. High humidity reduced the total plant dry matter and total leaf area, increasing the dry matter partitioning into the stems and reducing it into the leaves. However, the low-Ca supply did not affect those parameters. Plant Ca concentration was significantly reduced by low-Ca supply as well as by high RH, but to a much greater extent by the Ca supply than by high RH. Ca concentrations in leaves, stem, and roots were quickly reduced already after 1 day of low-Ca. After 14 days, Ca concentration in all plant organs (leaves, stems and roots) was reduced by approximately 70% compared to control plants. Our data show that calcium supply, and consequently Ca concentration in the tomato plant can be reduced drastically for short-term periods during the vegetative growth stage without any adverse effect on growth whilst higher humidity reduce both growth and Ca concentration in young vegetative tomato plants. Consequently, reduced Ca uptake at high air humidity is not the cause for the reduction in growth. Keywords: Calcium; Transpiration; Dry matter partitioning; Leaf expansion; Lycopersicon esculentum Mill
Vertical Farming: Moving from Genetic to Environmental Modification
Vertical farming (VF) is a novel plant production system that allows local production of high-quality fruits and vegetables for rapidly growing cities. VF offers a myriad of opportunities to move from genetic to environmental modification and to produce crops of guaranteed quality and quantity independent of weather, soil conditions, or climate chang
Far-red radiation increases flower and fruit abortion in sweet pepper (Capsicum annuum L.)
Fruit set is a crucial plant developmental process, determining yield in many crops. Pepper (Capsicum annuum L.) is a crop with poor fruit set as typically about two-thirds of all flowers abort. A higher light integral improves fruit set. However, the role of light spectrum has hardly been investigated. Opportunities for detailed investigation of light spectrum effects on fruit set have strongly increased with the introduction of narrow-band LED lighting. To investigate whether additional far-red light (FR) influences the fruit set of sweet pepper, a climate chamber experiment was conducted. Four light treatments were applied to pepper plants grown under 130 µmol m−2 s−1 of red/white LED light. Treatments consisted of different intensities of FR (0, 50, 100 µmol m−2 s−1) applied throughout the day or applied at the end of day (EOD, 30 min, 30 µmol m−2 s−1). Treatments resulted in phytochrome photostationary state (PSS) values of 0.88, 0.77. 0.70 and EOD 0.16, respectively. Fruit set was determined 3 weeks after the last anthesis of the studied flowers. Additional FR light reduced fruit set in sweet pepper, regardless of whether FR light was provided during the whole day or only at the end of the day. Meanwhile, FR led to more stem elongation, more upright branches, and more dry mass partitioning to stems. Additional FR during the daytime increased total shoot dry weight but not when FR was applied at the end of day. Possible reasons for stimulated flower and fruit abortion by additional FR are discussed
Unraveling the role of red:Blue LED lights on resource use efficiency and nutritional properties of indoor grown sweet basil
Indoor plant cultivation can result in significantly improved resource use efficiency (surface, water, and nutrients) as compared to traditional growing systems, but illumination costs are still high. LEDs (light emitting diodes) are gaining attention for indoor cultivation because of their ability to provide light of different spectra. In the light spectrum, red and blue regions are often considered the major plants’ energy sources for photosynthetic CO 2 assimilation. This study aims at identifying the role played by red:blue (R:B) ratio on the resource use efficiency of indoor basil cultivation, linking the physiological response to light to changes in yield and nutritional properties. Basil plants were cultivated in growth chambers under five LED light regimens characterized by different R:B ratios ranging from 0.5 to 4 (respectively, RB 0.5 , RB 1 , RB 2 , RB 3 , and RB 4 ), using fluorescent lamps as control (CK 1 ). A photosynthetic photon flux density of 215 µmol m −2 s −1 was provided for 16 h per day. The greatest biomass production was associated with LED lighting as compared with fluorescent lamp. Despite a reduction in both stomatal conductance and PSII quantum efficiency, adoption of RB 3 resulted in higher yield and chlorophyll content, leading to improved use efficiency for water and energy. Antioxidant activity followed a spectral-response function, with optimum associated with RB 3 . A low RB ratio (0.5) reduced the relative content of several volatiles, as compared to CK 1 and RB ≥ 2. Moreover, mineral leaf concentration (g g −1 DW) and total content in plant (g plant −1 ) were influences by light quality, resulting in greater N, P, K, Ca, Mg, and Fe accumulation in plants cultivated with RB 3 . Contrarily, nutrient use efficiency was increased in RB ≤ 1. From this study it can be concluded that a RB ratio of 3 provides optimal growing conditions for indoor cultivation of basil, fostering improved performances in terms of growth, physiological and metabolic functions, and resources use efficiency. </p
Functional—structural plant modeling of plants and crops
Crop models have been instrumental in predicting yields in wide ranges of current and future environmental conditions. However, they encounter problems in representing spatial heterogeneity of a plant stand and the associated plant responses to local conditions, as well as in simulating the effects of specific plant traits, management choices that influence plant architecture and lighting regimes such as those in greenhouses. For such purposes, functional–structural plant (FSP) models have been developed, which simulate individual plants that interact with each other in 3D, with the changes in plant architecture feeding back on the distribution of environmental drivers that make them grow and develop (light, water, nutrients). In this chapter, the authors outline the purposes of FSP models, the components they need to have in order to serve the purposes mentioned above and give an account of recent applications of such models
Green light reduces elongation when partially replacing sole blue light independently from cryptochrome 1a
Although green light is sometimes neglected, it can have several effects on plant growth and development. Green light is probably sensed by cryptochromes (crys), one of the blue light photoreceptor families. The aim of this study is to investigate the possible interaction between green and blue light and the involvement of crys in the green light response of plant photomorphogenesis. We hypothesize that green light effects on morphology only occur when crys are activated by the presence of blue light. Wild‐type Moneymaker (MM), cry1a mutant (cry1a), and two CRY2 overexpressing transgenic lines (CRY2‐OX3 and CRY2‐OX8) of tomato (Solanum lycopersicum) were grown in a climate chamber without or with green light (30 μmol m(−2) s(−1)) on backgrounds of sole red, sole blue and red/blue mixture, with all treatments having the same photosynthetic photon flux density of 150 μmol m(−2) s(−1). Green light showed no significant effects on biomass accumulation, nor on leaf characteristics such as leaf area, specific leaf area, and chlorophyll content. However, in all genotypes, green light significantly decreased stem length on a sole blue background, whereas green light hardly affected stem length on sole red and red/blue mixture background. MM, cry1a, and CRY2‐OX3/8 plants all exhibited similar responses of stem elongation to green light, indicating that cry1a, and probably cry2, is not involved in this green light effect. We conclude that partially replacing blue light by green light reduces elongation and that this is independent of cry1a
Non-structural carbohydrate dynamics and growth in tomato plants grown at fluctuating light and temperature
Fluctuations in light intensity and temperature lead to periods of asynchrony between carbon (C) supply by photosynthesis and C demand by the plant organs. Storage and remobilization of non-structural carbohydrates (NSC) are important processes that allow plants to buffer these fluctuations. We aimed to test the hypothesis that C storage and remobilization can buffer the effects of temperature and light fluctuations on growth of tomato plants. Tomato plants were grown at temperature amplitudes of 3 or 10°C (deviation around the mean of 22°C) combined with integration periods (IP) of 2 or 10 days. Temperature and light were applied in Phase (high temperature simultaneously with high light intensity, (400 μmol m(–2) s(–1)), low temperature simultaneously with low light intensity (200 μmol m(–2) s(–1)) or in Antiphase (high temperature with low light intensity, low temperature with high light intensity). A control treatment with constant temperature (22°C) and a constant light intensity (300 μmol m(–2) s(–1)) was also applied. After 20 days all treatments had received the same temperature and light integral. Differences in final structural dry weight were relatively small, while NSC concentrations were highly dynamic and followed changes of light and temperature (a positive correlation with decreasing temperature and increasing light intensity). High temperature and low light intensity lead to depletion of the NSC pool, but NSC level never dropped below 8% of the plant weight and this fraction was not mobilizable. Our results suggest that growing plants under fluctuating conditions do not necessarily have detrimental effects on plant growth and may improve biomass production in plants. These findings highlight the importance in the NSC pool dynamics to buffer fluctuations of light and temperature on plant structural growth
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