大「逆」不道—局部逆境下植物體內傳訊與物質分配機制
When a leaf of a plant encounters stress, how does the plant convey the stress signal to other tissues and manage nutrient distribution? This field of study has been largely unexplored. However, the unique interconnected frond structure of Lemna trisulca, along with the use of a divided Petri dish, is very suitable for handling localized stress and investigating the mechanisms of intracellular signaling and nutrient distribution. Research has shown that when the mother leaf experiences localized stress, it releases healthy daughter leaves to minimize collateral damage to the daughter leaves. Conversely, when the daughter leaves face localized stress, the mother leaf chooses to retain them and continues supplying them with nutrients to support their survival. In-depth studies revealed that stressed daughter leaves accumulate Reactive Oxygen Species (ROS), triggering nutrient distribution by sending a distress signal to the mother leaf. This prompts the mother leaf to use Ca2+ as a signaling molecule to deliver nutrients to the daughter leaves. Selective detachment is regulated and triggered by the interaction between Ca2+ and ROS within the mother leaf. When the mother leaf undergoes stress, Ca2+ acts upstream to induce ROS accumulation at the nodes, sending a unidirectional detachment signal to the daughter leaves. This causes ROS accumulation at the daughter leaf nodes, inducing detachment and thereby reducing the collateral damage the daughter leaf could experience due to the mother leaves.
Let There Be (Optimal) Light
On average, the agricultural sector uses 70% of water withdrawals worldwide to produce crops1 and contributes to the eutrophication of lakes by using nutrients that are leached from the soils into lakes and reservoirs2. Vertical farming has great potential to remedy some of these issues. By growing plants vertically in controlled environments with artificial light and reusing the water, vertical farms use op to 99% less water3 and can produce up to 10 times the yield per square meter4 compared to traditional greenhouses. This improved efficiency comes at a cost; on average, vertical farms use more than 600% more energy per kilogramme of crop compared to traditional greenhouses5. 55% of this energy use is due to the use of artificial lighting6. Even though a lot of research is conducted on yield optimisation of crops in vertical farming, few research articles focus on the growth efficiency of crops to reduce the energy use in vertical farms. Only a few previous studies have tested photoperiods under 10 h·d-1. This study focuses on reducing the energy costs of light use in vertical farms by finding the photoperiod with highest energy use efficiency for the leafy vegetable arugula (eruca sativa). Energy use efficiency is defined as fresh mass per unit of electricity input (measured in kWh). In this study, arugula plants were exposed to LED growth light, with photoperiods ranging from 0 h·d-1 to 24 h·d-1 (0 h·d-1, 4 h·d-1, 7 h·d-1, 9 h·d-1, 12 h·d-1, 14 h·d-1, 16 h·d-1 and 24 h·d-1) and a PPFD of 800 μmol·m-2·s-1. The photoperiod 7 h·d-1 had the highest energy use efficiency of all photoperiods and, if used in vertical farms, this could account for approximately a 10 percent decrease in energy per kilogramme used in vertical farms (a 4 kWh decrease), with the planting density of 1400 plants per m2. This could amount to a yearly energy saving of 4,000,000 kWh per vertical farm (based on the yearly harvest of the vertical farm Nordic Harvest). This could help make vertical farming a more sustainable plant production for the future and in turn, help farming protect our water resources instead of consuming and polluting.
大「逆」不道—局部逆境下植物體內傳訊與物質分配機制
When a leaf of a plant encounters stress, how does the plant convey the stress signal to other tissues and manage nutrient distribution? This field of study has been largely unexplored. However, the unique interconnected frond structure of Lemna trisulca, along with the use of a divided Petri dish, is very suitable for handling localized stress and investigating the mechanisms of intracellular signaling and nutrient distribution. Research has shown that when the mother leaf experiences localized stress, it releases healthy daughter leaves to minimize collateral damage to the daughter leaves. Conversely, when the daughter leaves face localized stress, the mother leaf chooses to retain them and continues supplying them with nutrients to support their survival. In-depth studies revealed that stressed daughter leaves accumulate Reactive Oxygen Species (ROS), triggering nutrient distribution by sending a distress signal to the mother leaf. This prompts the mother leaf to use Ca2+ as a signaling molecule to deliver nutrients to the daughter leaves. Selective detachment is regulated and triggered by the interaction between Ca2+ and ROS within the mother leaf. When the mother leaf undergoes stress, Ca2+ acts upstream to induce ROS accumulation at the nodes, sending a unidirectional detachment signal to the daughter leaves. This causes ROS accumulation at the daughter leaf nodes, inducing detachment and thereby reducing the collateral damage the daughter leaf could experience due to the mother leaves.