Dr. Lynette Morgan
Dr. Lynette Morgan holds a B. Hort. Tech. degree and a PhD in hydroponic greenhouse production from Massey University, New Zealand. Lynette is a partner with SUNTEC International Hydroponic Consultants and has authored five hydroponic technical books.
High-tech Propagation
The basic principles of plant propagation have been used for centuries, but these days, we have a whole host of new technology and knowledge to make the process faster and more reliable, and it’s only getting even more high-tech…
Ever since the dawn of agriculture, plant propagation techniques have been under intensive study. Without reliable methods of plant multiplication we would have no crops to harvest and no way of creating future generations of improved genetic stock. While the basic principles of plant propagation have been understood and used for centuries, these days we have a whole host of new technology, equipment, products and knowledge that have made vast improvements in the reliability and speed of this process. Furthermore, researchers are still delving into many aspects of plant multiplication and uncovering new information to further improve the process of propagation of a wide range of species.
As indoor gardeners we have a major advantage when it comes to propagation. With precise control over the environment, heat, humidity, light, oxygenation, CO2 and other factors, propagation becomes a more reliable process. Couple this with advances in hydroponic equipment and products specifically designed for the nurturing of new plants, seed production and treatment technology, and knowledge of root formation compounds, hydroponic growers have all the tools required for successful propagation.
While high-tech equipment provides some valuable assistance with propagation, growers still need some basic knowledge about the best methods to use for different species. Ideally, even beginner growers should be able to multiply plants via seeds and cuttings and clones as well as know which method is best for each crop. In the early days of gardening this was relatively simple. Growers would sow seeds or take cuttings and clones from plants, poke them into the soil someplace warm and hope for the best.Often the results were not great and a certain failure rate was to be expected. Nowadays we have come to expect a high success rate with propagation due to advances in technology, the indoor gardening environment and a great deal more information.
Clones or seedlings?
The two main methods of propagation used by indoor gardeners are via seed and via cuttings and clones. There is actually a large number of techniques used on different species for propagation, such as bulbs, rhizomes, corms, air layering, root layering, division, offsets and plantlets produced on stolons and others. However, the majority of vegetable and herb species we grow hydroponically are produced via seeds and cuttings.
The advantage of cuttings is that the resulting new plant will be genetically identical to the mother plant the material was taken from. This means all the good characteristics of the plant are retained and we know exactly what to expect in terms of growth and yields from the propagated plantlets. The disadvantage is that pests, diseases and viruses carried on the mother plant can be transferred to the daughter plants. Cuttings also require a mother or stock plant to be maintained in a healthy state for cuttings to be taken from, so genetic material can’t be stored for extended periods of time in the way that seeds can. Cutting material, depending on species, can take anywhere from a few days to many months to form new roots, although most of the species we grown indoors are relatively quick to do so. Cuttings are often a preferred way of multiplying plants that are very slow or unreliable from seed. For example, a stem cutting of mint will form roots in water in a few days, whereas the tiny seeds take many weeks to produce a seedling large enough to plant out.
Seeds have the advantage of being small, portable and easy to store for a relatively long period of time. Most vegetable and herb seed germinates quickly, within a few days for most, and commercially produced seed usually has a very high percentage germination rate. Hybrid seed will have uniform genetics and has been bred for adventurous characteristics. However, open pollinated seed will not produce new plants identical to the parents. As you can see, genetics can be fairly random when hybrid seed is not used.
Cuttings or clones?The technology
Some softwood species will easily root quickly, often in a jar of water; however, most species we want to clone benefit from some assistance, care and attention. After carefully selecting and preparing the cutting material from a healthy stock plant, a root promotion product should be applied. Back in the old days, there were just basic powders or solutions of an auxin hormone used by commercial propagators, these days we have a wide range of highly advanced and effective rooting compounds and bio stimulants formulated into easy to use gels, powders and solutions. Based on extensive research into root promotion compounds, rooting gels now contain not just IBA or NAA, which are auxin plant growth regulators, but also other stimulants and bioactive compounds shown to be beneficial for this process.
Auxin (IBA and NAA) are plant growth regulators which stimulate root development by inducing root initials that differentiate from cells of the young secondary phloem, cambium and pith tissue of the cutting material. IBA is most commonly used in these products as it is relatively stable and doesn’t break down due to enzymes within the plant. It’s well proven that use of a product containing an auxin such as IBA increases the percentage of rooted cuttings, the number of roots and the speed of root formation. However, advances in plant research over the last few decades and even quite recently have also discovered other root formation substances which are synergistic with IBA.
Since the 1950s it’s been known that boron (B) is essential for the development of adventitious roots on stem cuttings. Many researchers have found that whereas roots are initiated in response to auxin, boron was essential for the subsequent growth of roots. Thiamine (vitamin B1) is another root promotion substance in cuttings of many species. Studies have shown thiamine assists with promotion of rooting in terms of speed and number of roots formed. Many highly effective hydroponic rooting gels and other products contain boron, thiamine, humic or fulvic acids and a host of other vitamins, minerals and bioactive compounds that might be beneficial to root formation on cuttings.
More recently we have seen a range of microbial products being developed specifically to help promote root formation on cuttings and young seedlings. These microbial products are not new –the beneficial effect of mycorrhizal fungi on rooting of woody plant cuttings was reported in the 1970s; however, its only more recently that shelf-life stable and effective products have been available for smaller growers to purchase. These plant growth promoting rhizobacteria are thought to enhance root development either directly by producing phytohormones, or indirectly by inhibiting disease pathogens.
Along with increasingly effective rooting promotion gel products and bio stimulates, advances in propagation substrates and systems have seen sometimes miraculous improvements in percentage germination and cutting take rates. Root formation and germination are highly reliant on the correct environment as well as freedom from certain pathogens such as pythium and other root rot diseases. Sterile, highly aerated propagation media such as oasis, rockwool, foam substrates, coconut fibre, vermiculite and many new types of starter cubes are a vast improvement on trays of sand and peat historically used for propagation. Many of these new mediums have been created with specific air to water ratios to boost oxygen around the newly forming root initials or germinating seed.
Other new propagation products are highly specific to hydroponics and include a wide range of different sized propagation systems–often termed `cloning machines’that mist highly aerated water and nutrients inside a chamber, maintaining the optimum environment for root formation. These types of systems are particularly useful for harder wood cuttings and difficult on root species as they speed up the rate of root formation.
Seeds: the technology
Just as with cuttings, seed germination has also seen some advances in technology and specialised materials. Most hydroponic gardeners these days raise seedlings in specially designed propagation mediums. These can be sterile foams, rockwool, oasis or any of wide range of synthetic materials or more organically based mixes of coconut fibre, composts and propagation cubes made from a bound matrix of these materials. As with cuttings, there are a range of bio stimulant products for seed germination and seedlings, including those based on humic and fulvic acids, vitamin and minerals and microbial inoculants. Along with a suitable germination medium, growers can utilize a range of propagation equipment from the easy to use heating pad to an enclosed germination chamber which maintains the right degree of heat, humidity and light once the seedlings emerge.
Seed technology itself has also improved in modern times. Many small and difficult to handle seeds such as lettuce can be purchased in pelleted form. For species such as lettuce, thermo pelleting assists the seed to germinate in a wider range of temperature conditions, while other seeds can be coated in growth promotants or fungicides to help control pre- and post-germination rot pathogens. Other seeds might be primed to promote rapid germination and most are viability tested before they are sold.
Tissue culture: small-scale technology
A newer technology as far as home gardeners goes has been the introduction of home tissue culture kits and equipment. Tissue culture is a way of rapidly bulking up huge numbers of plants from a small amount of material and has largely been in the realm of commercial propagators for decades due to the requirement for aseptic conditions under which to carry this process out. Recent technology has seen the use of scaled down tissue culture equipment being used by small growers and indoor gardeners, although a certain degree of skill is still required to carry this process out correctly.
There are a number of different tissue culture methods; however, the most commonly used is called adventitious shoot formation, where a small piece of plant is taken (like a root, leaf, bulb, scale or similar) then induced to produce many small shoots through application of plant growth hormone contained in the tissue culture gel medium. Normally, such plant parts would not produce new shoots, let alone masses of them, but the conditions inside the tissue culture flask and the application of the plant growth regulator causes this growth to occur. These shoots, once sufficiently developed, are divided up into individual clumps and grown on in another flask where they are induced to form tiny roots by application of another plant growth hormone in the agar gel substrate. Then the plantlets are grown until they are large enough to leave the protected environment of the flask, be potted up and grown on as normal plantlets. This procedure can be used for a wide range of plants; however, beginners often start learning tissue culture methods using an easy species such as African violet.
Current technologies used to increase the speed and reliability of plant propagation are a major boost for keen indoor gardeners. From simple seed germination to advanced tissue culture, we have access to specific equipment and products to make this a fun and productive process. No doubt in the future we will see further advancements in propagation technology and tools as research into these plant processes is continually ongoing.
References and sources of information
R G Linderman and C A Call, (1977). “Enhanced rooting of woody plant cuttings by Mycorrhizal fungi”. J. Amer. Soc. Hort. Sci 102(5): 629-632.
E Benizri, E Baudoin and A Guckert, (2001). “Root Colonization by inoculated plant growth promoting Rhizobacteria.” Biocontrol Science and technolog Vol 11(5): 557-754.
W Middleton, B C Jarvis and A Booth, (1978). “The boron requirement for root development in stem cuttings of Phaseolus Aureus Roxb.” New Phytologist Vol 81(2): 287-297.
Furry Frustrations
In spite all our modern technology and information, hydroponic disease outbreaks still can get the better of us. So, here’s a primer on how to identify, get rid of and prevent molds and mildews in your growroom.
Despite all our modern technology, information sources and even some considerable experience with hydroponics, plant plagues and pestilence can still get the better of us. Although some problems are relatively easy to identify and cure, others can besiege us for weeks or, even worse, some pathogens just keep coming back year after year.
Newer growers are often confused with disease symptoms that look very much alike (and even some that don’t look so similar) and those don’t live up to their names—downy mildew, for example, often first shows as round yellow spots on the upper leaf surface. On the other hand, powdery mildew appears just as the name suggests: a sprinkling of white spores over the upper leaf surfaces. Nonetheless, it is sometimes confused with downy mildew, which is a completely separate disease with different control methods and conditions under which it develops. To complicate matters further, furry spores from a number of pathogens can be various shades of grey, cream, brown and black, making identification from furry growths alone a hit and miss process. And it’s easy to miss the sporulation when it occurs on the undersides of leaves.
Luckily, in the controlled environment of a well-run indoor garden, fungal and bacterial disease attack is less common than in outdoor or field crops, which are exposed to the elements and (in particular) the drenching effects of rain. Wet leaves and high humidity—which can’t be controlled outdoors—create a high disease pressure, as most fungal and bacterial pathogens need moisture to infect plant tissue. By modifying the environment effectively, we can significantly reduce the likelihood of any opportunistic disease spores being able to attack plants. While prevention of disease with correct climate control goes a long way towards a healthy crop, it unfortunately doesn’t always guarantee a problem will never occur; so, regular inspection of all plants in an indoor garden needs to be carried out. Most disease issues can be fairly easily controlled if found and dealt with early before any major damage is done.
Powdery mildew
Powdery mildew is perhaps the most common and frustrating of all the diseases encountered in an indoor garden, especially since commercial growers have noticed that powdery mildew—which was once relatively easy to eradicate with a few quick sprays—has become much more resilient to chemical control options and outbreaks can reoccur in rapid succession. Indoor gardeners might already be noticing the same problem.
Powdery mildew is easily recognized, although the first signs of a new infection might go unnoticed as they often occur inside dense leaf canopies. Powdery mildew creates the development of fine, whitish powdery deposits that look almost like a sprinkling of talcum powder over the upper leaf surface. As the disease progresses, entire leaves can be completely covered in this white mycelium growth—at which point the leaf will begin to yellow; dry, dead brown spots develop; and, eventually, the leaf will abscise from the plant. Stems and fruit can also become infected in severe cases.
The term powdery mildew is not just one disease, however; the name applies to the symptoms that develop. There are a number of different fungi genera that cause this powdery problem. Some powdery mildew fungi are specific to certain plants, while others have a much wider host range. Under protected cultivation in greenhouses and with indoor gardens, the most common species of fungi that cause powdery mildew symptoms are erysiphe, leveillula, microsphaera, podosphaera, odium and sphaerotheca, and possibly a few others. Erysiphe is common on lettuce and other salad green plants, and often the leaves show characteristic yellow patches after the appearance of the white mycelium growth. Leveillua occurs mostly on tomatoes and peppers, and might also produce fungal spores on the lower leaf surfaces and stems, as well as the upper surface. Leveillua on tomatoes is a little different from other powdery mildew species as it grows unseen within the leaf tissue for a latency period of up to three weeks from first infection.
Conditions for development of powdery mildew vary depending on the species of fungi. Most of the common powdery mildew species need high humidity (greater than 90%) for infection to occur, while leveillula infection on tomatoes and peppers can occur across a wide range of relatively humidity levels. Generally moderate to warm temperatures (68 to 86°F) favor infection. While high humidity does favor the development of many powdery mildew species, the greatest rate of infection and spread within a growing area occurs when humidity levels climb at night (thus allowing the spores to germinate and infect leaves) and then the less humid daytime air allows the newly produced spores to dry and be released into the air for further spread. So, control of humidity, particularly nighttime relative humidity levels (which are more difficult to deal with), is seen as one of the best tools for prevention of powdery mildew. Increasing air movement up, under and through the canopy often gives a good degree of mildew control, as does preventing of overcrowding and selective pruning to let air flow through the crop.
As with many diseases, genetic resistance is also one of the best forms of powdery mildew prevention; however, few crops have a wide selection of resistant cultivars to choose from. Many cucurbit plants (such as cucumbers and melons) have hybrid cultivars with a high degree of powdery mildew resistance and these should be selected wherever possible, as mildew is a very common and devastating disease on these crops. Some tomato cultivars have resistance to oidium species of mildew, but not to other forms, and certain ornamentals, such as zinnia, might also have resistant cultivars.
Since powdery mildew has its fungal hyphae and spores exposed on the leaf surface, it should—in theory—be easy to control with sprays (provided there is good and thorough leaf coverage). There are a few natural remedies, including spraying the foliage with milk and other weakly alkaline compounds to change the pH of the leaf surface, making it less desirable for the fungal spores to germinate. While these have been proven to have only a short-term and limited range of effect, sodium and potassium bicarbonates have been scientifically proven to be more effective for prevention of a number of common mildew-causing fungi species. Potassium bicarbonate has proven to be more effective than sodium bicarbonate and does not compound the problem with unwanted sodium runoff. Sodium and potassium bicarbonate do need to be used with care though, as overdosing plants with baking soda will burn the foliage severely. So, the general recommendation of 0.72 oz. per gallon or less should be followed.
Another highly effective compound is sulfur, either applied as a protectant fungicide (micronized sulfur) product or in a sulfur vaporizer. Sulfur works by a process of selective toxicity—that is, the sulfur is more toxic to the disease than to the host. However, sulfur needs to used with care. If applied when temperatures are too warm, it can cause considerable plant injury. Foliar sprays of silica, salicylic acid or chitosan also might help provide protection by providing a barrier to infection or by inducing the plant’s natural defense response to attack by powdery mildew.
There are also some biological fungicides, including those using suppressive beneficial fungi like Bacillus subtilis (serenade); however, results with these can vary somewhat depending on the environmental conditions, which need to be just right for the beneficials to grow and multiply before they can start suppressing the pathogen. Some growers have found that light sprays of horticultural oils or neem oil have assisted with powdery mildew control, but many research studies have found these are not very effective.
Many chemical fungicides are still highly effective if used correctly and rotated so that disease resistance does not build up. The effectiveness of different fungicides can vary significantly with the particular powdery mildew species and the crop being grown, so if one product does not appear to be working, another should be tried. Keep in mind that eradication fungicides need to be used as soon as the first powdery signs are seen as early control is critical. It is also important to check the label of spray products; many are only registered for use on ornamental crops and should not be applied to food-producing plants, and others may have withholding periods which must be waited out before the plants can be harvested and consumed
As with most disease, successful control of powdery mildew doesn’t just involve one quick fix spray. To get complete control, the environment, plant density, humidity levels, air movement, genetic resistance, natural, biological and chemical control compounds all have something to offer—and often more than one approach will be needed to get the mildew monsters under control.
Downy mildew
Downy mildew is a completely different disease from powdery mildew, although the two are often mistaken. It can be a major issue, particularly on lettuce and some annuals and flowering ornamentals under certain conditions. Downy mildew produces fine greyish-white powdery patches on the underside of the lowest leaves (it will then progress up the plant if the disease remains uncontrolled). Nonetheless, the first symptom of a downy mildew outbreak is the appearance of light green to yellow spots bordered by the leaf veins on the older foliage. Often, the appearance of these yellow spots is not linked to a downy mildew infection until the furry spore-producing bodies pop up on the undersides of the leaf. Downy mildew is common in greenhouses in winter, as periods of cool temperatures and high humidity (where leaves remain damp) encourage the mildew to attack. The spread of downy mildew spores is maximized when night temperatures are between 41 and 50°F, with day temperatures of 54 to 68°F). Under these favorable conditions, the disease can progress from infection to sporulation (and spread via spores) in less than five days.
Control of downy mildew involves selecting genetically resistant cultivars wherever possible, modification of the growing environment and the use of fungicide rotational spray programs (downy mildew, just like powdery mildew, is capable of developing fungicide resistance). The main environmental control option that is usually successful in controlling downy mildew is to increase air temperature (above 77°F) and reduce humidity levels at night while also avoiding getting the foliage wet and increasing ventilation. For those who don’t wish to spray fungicides in their indoor gardens, any plant that shows symptoms of downy mildew should be removed from the growing area and destroyed to prevent spores spreading to other plants and creating an epidemic. Good hygiene practices, including wiping and washing all surfaces with a strong disinfectant and removing all plant debris, will also help prevent any carry-over of disease from one crop to the next.
Grey mold (botrytis)
Another common fungal disease that also develops greyish furry patches on stems, leaves and fruit—and is sometimes mistaken by new growers for downy mildew or other rot pathogens—is grey mold (Botrytis cinerea). It has a wide host range, from lettuce, tomatoes and peppers to a wide range of annuals and ornamentals, herbs and strawberries (pretty much any plant we could choose to grow). Botrytis can infect plants right from the early seedling stage and might cause damping off through all stages of the plants development, and it can even cause rots in harvested produce during storage.
Botrytis spreads by air-borne conidia—spores that germinate on leaf surfaces when conditions are wet or humid. The conidia germinate and rapidly penetrate the leaf surface cells, especially where damage might have occurred through leaf trimming or other wounds. Botrytis can also infect any rotting or dying older tissue present on the plant. After infection, the first visible signs of this disease appear as brown water-soaked areas, from which the grey or brown mycellial growth (which sometimes resembles fine ash) forms. Conditions that favor botrytis development are high humidity (above 95%) and cooler temperatures, and the disease becomes much more severe where damp stagnant air forms and where there is insufficient air movement and ventilation.
Botrytis is a disease that has, over the years, developed multiple resistances to a wide range of chemical fungicides, making many sprays ineffective for control. The first form of defense should be modifications to the growing environment, increasing air flow, venting out moist air rapidly, particularly at night when condensation would otherwise form. Taking care with plant density is also important, as overcrowding often leads to botrytis problems, and any leaves that show the first signs of grey mold infection should be removed before the spores have a chance to mature, become air-borne and infect surrounding plants. Preventing overfeeding with nitrogen, which creates soft succulent growth prone to fungal infection, and maintaining good levels of foliar calcium are important to produce plant tissue strong enough to prevent opportunistic infection. Some beneficial fungi have been formulated into products that can be sprayed onto plants to act as antagonists to botrytis, including formulations containing Trichoderma harzianum spores. Using silica, salicyclic acid and other plant strengthening agents as both foliar sprays and in the nutrient solution might also offer some production against botrytis and other fungal pathogens by inducing the plant’s natural defense mechanisms.
Furry sporulating diseases might seem like a formidable foe; however, many outbreaks are due to a combination of problems with environmental control (humidity and stagnation of the air flow) and a source of active infection from other plant material, crop debris or spores left over from a previous outbreak. So, cleanliness, attention to growing environment, preventing overcrowding and knowing what the early signs of an outbreak look like are all vitally important for controlling these furry plant invaders.
Riding the Shortwave
Light—we all know it’s what powers photosynthesis and growth; however, a plant’s response to different parts of the light spectrum is wide and varied and much more complex than photosynthesis alone.
Light provides a source of external information to plants, which have a series of photo receptors that sensing parameters such as intensity, direction, photoperiod, spectrum and wavelength. Different parts of the light spectrum can cause different physiological and morphogenetic responses, many of which vary from species to species. This allows growers to use high-tech lighting to tailor the light spectrum towards desirable plant characteristics (while the exact details of the potential of customised wavelength lighting are still being researched and understood, this concept is already well accepted by many indoor gardeners).
Ultraviolet wavelengths
While we are aware of the wavelengths that power photosynthesis (blue—450 to 495 nm—and red—629 to 750 nm—light), other wavelengths are sensed by different receptors in plants and might help control normal plant growth and function. Of particular interest these days is ultraviolet (UV) shortwave light. Also known as electromagnetic radiation, this light has a wavelength that is shorter than that of visible light but longer than that of X-rays. It is the range 10 to 400nm. Within this range, UV is divided into a number of band spectrums, including UV-C (below 280 nm), UV-B (280 to 320 nm) and UV-A (320 to 400nm). UV is a natural part of sunlight and while humans can’t see UV light, some insects and birds can.
When we think of UV light most of us are reminded of sun burn, skin damage, genetic mutation and other negative affects; however, small doses of UV are also beneficial for humans as it is responsible for vitamin D synthesis. When it comes to plants, UV has been known for some time to have harmful effects plants, but in certain plant species, it seems that small doses can have some very beneficial effects (most of which we are only just starting to understand). For example, it’s only recently that it was discovered that plant roots can sense UV-B and use it as a signal between cells, which helps young plants with seedling morphogenesis and normal growth patterns (as with all plants, too much UV light can be toxic, and only small doses are required to activate receptors in plant tissue). Still, this of particular interest for both greenhouse and indoor gardeners—both who have more control of light intensity and wavelength than ever before as they are able to pick and choose from different lamp types and greenhouse films in order to provide varying degrees of UV shortwave light.
UV and protected cultivation
When exposed to UV, plants can produce a range of defence proteins that are similar to those activated when a plant is physically damaged. Shortwave light in the UV bands acts as a stress factor on plant growth and is therefore able to induce a wide range of plant growth and developmental characteristics. For example, UV-B light has been shown in a number of studies to reduce plant height and cause the development of smaller, thicker and shorter leaves (a typical stress response in plants). While this type of growth effect may be useful in a number of crops where a short, compact plant form is desirable, such as with potted flowering ornamentals, it might not be an advantage for others. Also, plants can increase their production of these defence proteins as the level of UV light increases up to a point where cell damage starts to become severe.
In greenhouse horticulture, there has been the development of a range of cladding films that have incorporated into the polythene material specific spectral filters designed to block or allow through certain wavebands. This finding has an obvious and significant benefit to growers of all crops as a reduction in the use of plant protection chemicals and compounds is a major advantage in commercial production. In contrast, some studies have found certain greenhouse pests (such as whitefly) to be significantly reduced under UV-blocking film claddings. However, at the same time, filtering out all UV might have negative effects on certain aspects of plant growth. Most commercial greenhouse production is still carried out under standard horticultural-grade plastic or glass claddings that block some of the UV wavelengths, allowing other short wavelengths through. In the future, we can expect to see the development of different greenhouse films for different crops and purposes based on their UV penetration category.
One of the most interesting and commercially important findings regarding UV light is the effect on the production of anthocyanin, which gives the deep red pigmentation in red lettuce cultivars and similar coloured plants. It has been found that red lettuce (Lollo rosso) grown under greenhouse films that transmit UV light (transparent above 280nm) had eight times more anthocyanin content, and hence a significantly deeper red colour than those grown under UV-blocking greenhouse films. It was also found that total red pigmentation was highest in lettuce when both UV-A and UV-B wavelengths were provided together rather than when just UV-A was provided on its own. Anthocyanin production in many plants has also been found to be stimulated and increased when UV light was supplemented with use of lamps producing short wavelengths in the UV region. Some studies have reported that other compounds such as beta carotene, which gives the orange colour in fruits and vegetables, is also stimulated by UV light. Plants produce these antioxidants to protect themselves from the negative effects of shortwave light exposure. For producers of red lettuce and other salad plants where a strong pigmentation is essential for marketability, this is an important finding as the penetration of UV (both as UV-A and UV-B) light down to the crop is likely to be just as essential as the initial selection of highly coloured cultivars to maintain anthocyanin levels.
As well as increased anthocyanin and plant colouration, exposure to shortwave UV light has been found to have a range of other benefits. In many species, UV light is an important contributor to flavour and aromatic compounds. Overall higher levels of secondary metabolites are produced under UV and it is thought that when both UV-A and UV-B wavelengths are present, plants accumulate secondary products that protect them from damage to the photosynthetic systems. These secondary metabolites are thought to include UV-protecting or -absorbing compounds that prevent some of the damage to cells and DNA caused by UV radiation reaching the photosynthetic apparatus. This means that the photosynthesis systems are not as damaged as we would expect with exposure to UV radiation. However, in some studies it has been found that damage can still occur to photosystem II in particular under UV wavelengths. In certain species, this causes a reduction in growth; so, it is possible that under UV wavelengths, the plant might divert some of its photosynthetic energy into producing compounds to protect it, thus reducing overall growth slightly. In yet other studies, no significant effect on growth reduction was seen when UV light was provided, so it’s likely any negative effects are species and environment dependant.
These protective secondary metabolites are likely to include flavonoid and phenolic compounds, many of which are also of interest for human health benefits. Anthocyanins, flavonoids and phenolics provide the anti-oxidant activity in fruits and vegetables, which are linked to a range of health promoting effects and prevention of degenerative diseases. More recently, the possibility of producing commercial crops with increased beneficial compounds under greenhouse films that transmit sufficient UV has been under investigation.
What does this mean for indoor gardeners?
While plants will grow and yield perfectly well under the tried and true red and blue spectrums of photosynthetically active radiation (PAR), there does exist the potential to provide specific supplementary short wavelengths where they provide benefits to certain species. Enhancing the deep red colouration in those plants that require high levels of anthocyanin production—such as red lettuce, ornamentals with highly coloured leaves and others grown indoors—would be one such use. Another might be to promote short, stocky, compact plant growth, an advantage in the confined space of an indoor garden where height restriction is a bonus. Increased resistance to pest and disease attack with harder, tougher plants and an activation of the plants’ natural immune response by UV wavelengths could be seen as another major benefit of including some shortwave radiation in the plants’ smorgasbord of light.
Many full-spectrum bulbs, fluorescents and other commonly used lamps still provide some UV output, although it pays to check the spectral output to ensure this is in the correct wavelengths of UV-A and UV-B. Despite the potential benefits, the use of UV wavelengths must be considered with some caution: while plants can generate secondary metabolites to protect themselves against low levels of UV, people can’t do the same thing. UV is still an issue with damaging sensitive human skin, so sunscreen protection might be required when working under UV for prolonged periods of time. Also, we need to remember that research studies have shown that both UV-A and UV-B wavelengths should be used together as they have a synergistic effect on plant response. Supplying just some UV-A might give no response and no benefit, while UV-A and UV-B together produce a much greater accumulation of flavonoids and other beneficial compounds. So, while shortwave UV won’t necessarily increase growth, it seems to have certain advantages that can’t be ignored when we consider how complex the interaction of plants and wavelengths actually is.