Plants can detect the presence of their neighbours and modify their growth behaviour accordingly. But the extent to which this neighbour detection is mediated by abiotic stressors is not well known. In this study we tested the acclimation response of Zea mays L. seedlings through belowground interactions to the presence of their siblings exposed to brief mechano stimuli. Maize seedling simultaneously shared the growth solution of touched plants or they were transferred to the growth solution of previously touched plants. We tested the growth preferences of newly germinated seedlings toward the growth solution of touched (T_solution) or untouched plants (C_solution). The primary root of the newly germinated seedlings grew significantly less towards T_solution than to C_solution. Plants transferred to T_solution allocated more biomass to shoots and less to roots. While plants that simultaneously shared their growth solution with the touched plants produced more biomass. Results show that plant responses to neighbours can be modified by aboveground abiotic stress to those neighbours and suggest that these modifications are mediated by belowground interactions.
Plants are well known for their deceptive ways, orchids being the worst of the bunch
The non-photosynthesizing orchid species Gastrodia pubilabiata mimics rotting mushrooms or fermented fruit, and is pollinated by fruit flies who mistakenly lay their eggs in its flowers. If there are rotting mushrooms near the orchid, its pollination rate increases. As well as using mushrooms to attract insect pollinators, G. pubilabiata survives by absorbing nutrients from the fungal hyphae of mushrooms. This is the first time a plant has been discovered to depend on mushrooms both above and below ground. more…
Mimosa leaves, pea tendrils, Venus flytraps and sundew traps all lost both their autonomous and touch-induced movements after exposure to anaesthetics. In Venus flytrap, this was shown to be due to the loss of action potentials under diethyl ether anaesthesia. The same concentration of diethyl ether immobilized pea tendrils. Anaesthetics also impeded seed germination and chlorophyll accumulation in cress seedlings. Endocytic vesicle recycling and reactive oxygen species (ROS) balance, as observed in intact Arabidopsis root apex cells, were also affected by all anaesthetics tested.
Allelopathy is the release of organic chemicals that help or harm plants growing nearby by a plant. What is really interesting is that these allelochemicals are not used by the plant except to influence other plants.
One of the best known cases of this happens with walnut trees. Walnut trees produce hydojuglone. When hydrojuglone is exposed to oxygen it causes anything from wilting to death in plants near the walnut tree.
While digging around the net learning about allelopathy I started to wonder just how smart plants might be and stumbled upon: Aspects of Plant Intelligence a paper published in the Annals of Botany in 2003
The more we learn about plants and the chemical signaling inside and sent out from the plant, the less like vegetables they appear to be.
The paper is very readable, you won’t need a science degree to dig through it and worth a read. You’ll not look at your plants the same way again.
The tip of the leaf of a plant senses blue light and signals the plant to grow in the direction of the blue light.
The red glow of a sunset is what signals the plant when it is time to bloom. A plant kept in a dark closet can be signaled to flower with just a short flash of red light.
Plants use both blue and red light to feed themselves but slightly favor red.
Plants appear mostly green because they are reflecting most of the green light that hits them, it doesn’t get used by the plant.
If your plant is not growing well, try adding more blue light. If you’re not getting flowers try more red light.
Plants release hundreds of volatile chemicals ( scents ) to both attract and repel insects.
Cabbage butterflies lay their eggs in cabbage. In response the cabbage plants release a scent that attracts two species of moths that feed on cabbage butterflies.
When insects lay eggs in the plant they damage the plant, this damage triggers the plant to release chemicals to protect it from the insects about to hatch and feed on the plant. Some chemicals kill the plant tissue around the egg causing the egg to fall off the plant. Other chemicals attract predators of the insect eggs.
Cabbage family plants make glucosinolate from sugar giving them their well known bitter flavor. This is what acts to fight cancer in people who eat these plants.
Plants containing glucosinolate can be used keep pests away from other crops.Some insects have adapted to be able to deflect the toxins and use these plants for feeding and egg laying.
In short: Plants measure the amount of red and blue light reaching their leaves. When that light falls to too low of a level the plant releases hormones which allow it to shoot up past the plants around it so it may get more light.
Plants grow in dense vegetations at the risk of being out-competed by neighbors. To increase their competitive power, plants display adaptive responses, such as rapid shoot elongation (shade avoidance) to consolidate light capture.
These responses are induced upon detection of proximate neighbors through perception of the reduced ratio between red (R) and far-red (FR) light that is typical for dense vegetations. The plant hormone auxin is a central regulator of plant development and plasticity, but until now it has been unknown how auxin transport is controlled to regulate shade-avoidance responses.
Here, we show that low R:FR detection changes the cellular location of the PIN-FORMED 3 (PIN3) protein, a regulator of auxin efflux, in Arabidopsis seedlings. As a result, auxin levels in the elongating hypocotyls are increased under low R:FR. Seedlings of the pin3-3 mutant lack this low R:FR-induced increase of endogenous auxin in the hypocotyl and, accordingly, have no elongation response to low R:FR.
We hypothesize that low R:FR-induced stimulation of auxin biosynthesis drives the regulation of PIN3, thus allowing shade avoidance to occur. The adaptive significance of PIN3-mediated control of shade-avoidance is shown in plant competition studies. It was found that pin3 mutants are outcompeted by wild-type neighbors who suppress fitness of pin3-3 by 40%. We conclude that low R:FR modulates the auxin distribution by a change in the cellular location of PIN3, and that this control can be of great importance for plants growing in dense vegetations. paper