Different LED light spectra’s and nano-chelated potassium affect the quality traits of Dolce Vita cut roses in soilless culture condition

Roses are classified as neutral day plants, but high light and cool temperatures produce high quality flowers in roses. As light quantity, the light quality and its special spectra can affect the flower yield and quality. This research aimed to study of the effect of LED light (control (sunlight), blue and red spectra’s) and nano-chelated potassium at three levels (0, 1.5 and 3 g/l) on some morphophysiological and biochemical traits of Rosa hybrida cv. Dolce Vita. Light and nano-chelated potassium treatments have a significant effect on most traits measured in the present study. According to the results, the use of red light and nano-chelated potassium in rose cultivation improved the quality characteristics and increased vase life. The highest fresh and dry weight of flowering branch and plant height was observed in red light treatment and the concentration of 3 g/l nano-chelated potassium. Biochemical parameters such as phenolic compounds, leaf and petal flavonoids, petal anthocyanin content, antioxidant capacity and vase life were also significantly increased under red light and with the concentration of 3 g/l nano-chelated potassium compared to the control. In general, it can be said that the use of red light and a concentration of 3 g/l nano-chelated potassium, can be effective in improving the quality of rose flowers, especially in low light condition.


Materials and methods
Plant material and experimental design. This research was conducted in the greenhouse unit and research laboratories of the horticulture department of Urmia University, Urmia, Iran. Newly grafted rose seedlings of Dolce Vita cultivar were purchased from a local commercial nursery and each seedling was planted in a 10 L plastic pot containing peat moss and perlite in a ratio of 75 to 25 percent. The pots were transferred under drip irrigation system and plants fertigated with a modified commercial rose fertilizing recipe using a pulse irrigation strategy five times a day. The potassium content of used recipe reduced to half strength and final nutrient solution contained 150 mg/l N, 45 mg/l P, 125 mg/l K, 120 mg/l Ca, 40 mg/l Mg and also trace elements. More details showed in Table 1.
Experimental treatments included foliar application with nano-chelated potassium 27% at three levels (0, 1.5 and 3 g/l) and light at three levels (control (sunlight), blue and red spectra's) as supplementary light that was performed as factorial in a completely randomized design with six replications. The nano-chelated potassium prepared by the method described by Nido et al. 17 . For this, a four step process ran including the preparation of potassium alginate solution, pre-gelation, stabilization and equilibration. For the preparation of potassium alginate solution (K-ALG), 117.5 ml of alginate stock solution (6 mM sodium alginate, pH 4.9) was mixed with KCl (as potassium source) and sonicated in Elmasonic P 120 H sonicator for 20 min. To form pre-gel, 36 mM calcium chloride solution (pH 7) was added drop by drop to K-ALG while sonicating at 25 °C. On stabilization step, 25 ml of chitosan stock solution (CHI), prepared by dissolving 0.10 mg/ml low molecular weight chitosan in 1% acetic acid, was added dropwise to K-ALG-CHI mixture while stirring for 30 min. For chemical reaction completion, the prepared mixture was kept for 24 h at room temperature and finally, the solution was ovendried at 75 °C for 1 h to obtain solid fertilizer. The potassium content assayed by Jenway PFP7 flame photometer. Chemical materials used in this method, were purchased from Sigma-Aldrich chemicals Company. The application of nano-chelated potassium and lighting treatments started just one week after first stem bending and when the new shoots reached to 3-4 cm height. Nano-chelated potassium used once a week as foliar application. The using of red and blue light as supplementary light started simultaneously with the application of nano-chelated potassium. Supplementary LED lighting as red and blue light used with the intensity of 95 µmol m −2 s −1 (Fig. 1). Total light intensity was about 530 µmol m −2 s −1 at the growing point of plants. Day/night temperature was adjusted to 27/22 °C during growing period and the relative humidity maintained at 55%. Plant samples were taken to evaluate the morphophysiological and biochemical characteristics. Petal anthocyanin. The anthocyanin content of petals in all extracts was measured by spectrophotometer and pH-differential method 19 using two buffer systems, potassium chloride buffer (0.025 M, pH = 1) and sodium acetate buffer (0.4 M, pH = 4.5). The results were expressed in milligrams per liter equivalent to cyanidin-3-glycoside in the extract based on the following formula: The density of monomeric anthocyanin pigment in the extract in mg/l is equal to (Ɛ × 1) (A × MW × DF × 1000), in which DF, MW, Ɛ and A refer to sample dilution factor, Molecular weight of cyanidin, Molar coefficient of cyanidin, and the amount of adsorption, respectively. The amount of absorption is calculated as follows: The A 510 and A 700 represent absorbance of 510 nm and 700 nm, respectively. Chlorophyll content. Photosynthetic pigments measurement was done using Gross 20 method and the absorbance was read at 645 and 663 nm using a spectrophotometer (UV/Visible Lambda 25 Perkin Elmer). The amount of chlorophylls a, b and total were calculated from the following equations and reported in mg/g fresh weight.
In the above relations, OD 663 and OD 645 are the absorption rates at 663 and 645 nm, respectively. Antioxidant capacity. DPPH method was used to measure antioxidant capacity. To measure the ability of extracts to inhibit free radicals (DPPH), first 100 μl of methanolic extract was mixed with 1900 μl of DPPH and then the samples were placed in the dark at room temperature for 30 min. Then, the absorbance of the samples was read by spectrophotometer at 517 nm and expressed by the percentage of inhibition 21 . Ac = control absorption. As = sample absorption.
Inhibition percentage = (Ac − As)/Ac * 100%  Petal phenolics. Total phenolic content was measured using Folin-Ciocalteu reagent method described by Marinova et al. 22 with some minor modifications in weight of plant sample and dilution factor. The absorbance of the samples was read at 750 nm. The standard curve of Gallic acid was used to calculate the amount of total phenol content and the amount of phenol was calculated based on the standard curve of Gallic acid using the following equation in milligrams of Gallic acid per gram of fresh weight. Y = a number read on a spectrophotometer. X = amount of phenol in mg/g fresh weight.
Flavonoids content of leaves and petals. Aluminum chloride colorimetric method 23 was used to measure flavonoids content in leaves and petals. The absorbance of the samples was read at 415 nm. The total flavonoids content of the samples was expressed in mg equivalent to quercetin per gram of plant dry weight.
Petal H 2 O 2 content. The amount of H 2 O 2 measured using a method described by Velikova et al. 24 . The sample absorbance was read at 390 nm and a standard curve was used to calculate the hydrogen peroxide concentration and the results were presented in micromoles per gram of fresh weight.
Leaf protein content. Bradford method 25 was used to determine the amount of soluble proteins. The reading was performed with a spectrophotometer at 585 nm. The amount of protein was calculated after drawing the protein standard curve and was expressed in milligrams per gram of fresh weight using the following equation.
y is the value read in the spectrophotometer and x is the value to be calculated.
Carbohydrate content. 0.5 g of leaf tissue was used to measure dissolved sugars according to Irigoyen et al. 26 method. To drawing the glucose standard curve, solutions of glucose with concentrations of 0 to 120 mg/l were prepared and all experimental steps were performed on them, and finally the absorbance was read at 625 nm.
Ethical approval. Authors confirm that all methods used in this study were performed in accordance with the relevant international and/or institutional guidelines and regulations.

Results
Flower stem height. Based on ANOVA the interaction effect of light and nano-chelated potassium was significant on flower stem height ( Table 2). As shown in Fig. 2a, the highest flower stem height (100 cm) was observed in the red light treatment and a concentration of 3 g/l nano-chelated potassium.
Flower stem FW and DW. The interaction of light and nano-chelated potassium treatments caused an increase in the fresh weight of the flower stem. The highest fresh weight of flower stem (120.31 g) was observed in red light treatment and concentration of 3 g/l nano-chelated potassium, which significantly increased in compared to the control (80.48 g) (Fig. 2b). Light treatment increased the dry weight of flower stem that red light treatment had a greater effect (32.32 g) on increasing dry weight of flower stem. The lowest dry weight of flower www.nature.com/scientificreports/ stem (23.01 g) was observed in the control (Fig. 2c). According to Fig. 2d, it was found that nano-chelated potassium treatment increased the dry weight of flower stems. The concentration of 3 g/l nano-chelated potassium had the greatest effect on increasing the dry weight of flower stems.
Stomata width. Based on our findings, light treatment increased the stomata width and as shown in Fig. 2e, the treatment of red and blue light on the stomata width was not statistically significant, but they had a signifi- www.nature.com/scientificreports/ cant difference with the control (29.44 µm). Increasing the concentration of nano-chelated potassium increased the stomata width so that the concentration of 3 g/l caused the highest stomata width (40 µm) which increased in compared to the control (Fig. 2f).
Leaf area. According to the results from the ANOVA, it was found that the interaction of light treatment and nano-chelated potassium caused an increasing trend in leaf area. According to Fig. 2g, the highest leaf area (13,240.5 mm 2 ) was observed in red light in combination with the concentration of 3 g/l nano-chelated potassium that resulted in a 1.68 times increase in leaf area compared to the control.
Leaf thickness. The results showed that the combination of light and nano-chelated potassium treatments reduced leaf thickness in treated plants. As shown in Fig. 2h, the highest leaf thickness (0.440 mm) was observed in the control treatment and the lowest leaf thickness (0.196 mm) was observed in red light treatment with 3 g/l nano-chelated potassium.
Stomatal conductance. The interactions of light and nano-chelated potassium has a significant effect on stomatal conductance at 1% probability level ( Table 2). Results showed that light and nano-chelated potassium treatment increased the stomatal conductance so that the highest stomatal conductance (316.53 mmol CO 2 m −2 s −1 ) was observed in red light treatment and concentration of 3 g/l nano-chelated potassium, Although there was no statistically significant difference between red light treatments with concentration of 1.5 g/l and blue light treatments with concentration of 3 g/l thousand nano-chelated potassium. The lowest stomatal conductance was observed in the control treatment. As Fig. 3a shows, the treatment of red light and nano-chelated potassium resulted in an increase in stomatal conductance compared to the control.
Total chlorophyll content. Total chlorophyll content significantly was affected by the interaction of light and nano-chelated potassium treatments. Light and nano-chelated potassium treatment increased the total chlorophyll content. According to Fig. 3b, it was found that the application of 3 g/l nano-chelated potassium in presence of blue light resulted in highest total chlorophyll content (3.95 mg/g FW). Although there was no statistically significant difference between recent treatment and concentration of 1.5 g/l nano-chelated potassium combined with red light. The lowest amount of total chlorophyll content (1 mg/g FW) was observed in the control.
Photosynthesis rate. The findings of this research showed that both red and blue light combined with nano-chelated potassium leads to an increase in photosynthesis rate. Blue and red light treatments and concentrations of 1.5 and 3 g/l nano-chelated potassium caused an increase in photosynthesis rate up to 8.44 µmol CO 2 m −2 s −1 , which shows a notable increase in compared to the control (2.05 µmol CO 2 m −2 s −1 ) (Fig. 3c).
Leaf protein content. It was found that the combined treatment of light and nano-chelated potassium led to an increase in total protein content. As shown in Fig. 3d, increasing the concentration of nano-chelated potassium and light treatment caused an increasing trend in total protein content. Red light treatment and concentration of 3 g/l nano-chelated potassium gave the highest amount of total protein content (9.72 mg/g FW). The lowest amount of protein (3.4 mg/g FW) was observed in the control. According to Fig. 3d, it was found that the red light treatment and a concentration of 3 g/l nano-chelated potassium resulted in an almost threefold increase in total protein compared to the control.
Carbohydrate content. Comparison of data means showed that red light treatment increased the amount of soluble carbohydrates and the plants exposed to red light treatment had the highest amount of soluble carbohydrates (686.22 mg/g FW). The lowest amount of soluble carbohydrates (485.77 mg/g FW) was observed in blue light treatment (Fig. 3e). According to Fig. 3f, it was found that nano-chelated potassium treatment increased the amount of soluble carbohydrates. Concentration of 3 g/l nano-chelated potassium had the greatest effect on increasing the amount of soluble carbohydrates, compared to the control.
Petal anthocyanin content. The results of ANOVA showed that petal anthocyanin content was affected significantly by the interaction of light and nano-chelated potassium treatments (Table 2). Combined application of light and nano-chelated potassium led to an increase in petal anthocyanin content. The highest amount of petal anthocyanin content (18.60 mg/g FW) was earned with application of 3 g/l nano-chelated potassium in the presence of red light. The lowest amount of petal anthocyanin (9.93 mg/g FW) was observed in the control treatment (Fig. 3g).
Petal phenolic content. Based on our findings, red light in combination with 3 g/l nano-chelated potassium had the greatest effect on the petal phenolic content increasing that was 140.92 mg gallic acid/g FW, which shows an increase in petal total phenolics compared to the control ( Table 3).

Flavonoids of leaves and petals.
Results showed that the interaction of light and nano-chelated potassium treatments led to an increase in leaf and petals flavonoids. As shown in Table 3, the highest amount of leaf and petals flavonoids was gained in presence of red light and the concentration of 3 g/l nano-chelated potassium and the lowest amount was observed in the control treatment.  (Table 3).

Scientific Reports
Petal H 2 O 2 content. According to the results of ANOVA, the effect of light treatment on hydrogen peroxide content of petals was significant at the probability level of 1% ( Table 2). Comparison of the means showed

Flower vase life.
Our findings showed that the combined use of light treatment and nano-chelated potassium led to an increase in flower vase life. As Table 3 shows, the highest vase life (26 days) was observed in the treatment of red light in combination with the concentration of 3 g/l nano-chelated potassium. The lowest vase life (13.66 days) was observed in the control treatment.

Discussion
Biomass & morphophysiological traits. Based on our findings, as seen in Fig. 2a-d, the use of nanochelated potassium and red light led to an increase in the height of the flower stem, as well as an increase in its fresh and dry weight and the leaf area. In confirmation of the present research, in the study conducted by Poudel et al. 27 , the length of stem and internode and the number of leaves of grape seedlings grown in red LED light were higher compared to those grown at blue LED 28 .
In the present study, as seen in Fig. 3a, red light treatment led to an increase in stomatal conductance. Zeaxanthin is one of the components of the xanthophyll cycle in chloroplast, increases in the light, and decreases in the dark. On the other hand, red and blue light reduces the acidity of the lumen and therefore increases the content of zeaxanthin 29 ; that is, it stimulates stomatal opening, resulting in more stomatal conductance, while darkness and green light prevents stomatal opening 29,30 . Potassium plays a crucial role in turgor regulation within the guard cells during stomatal movement 31 . As a rapid transport of K + from the guard cells into the leaf apoplast resulted in stomatal closure, it is reasonable to think that K-deficient condition may disturb stomata opening. The inductive effect of K + deficiency on stomatal closure and inhibited photosynthesis has been reported in several crop plants 32,33 .
Height increase due to the presence of blue light in some plants such as chrysanthemum (Chrysanthemum morifolium) 34 , parsley (Petroselinum crispum) 35 , petunia (Petunia × hybrida) 36 , and height reduction in plants such as Arabidopsis 37 , and poinsettia (Euphorbia pulcherrima) 38 has been reported which shows different plants react differently to the blue light spectra. Blue light affects the expression and function of some genes responsible for gibberellin metabolism (such as GA20ox), and in some plant species, it leads to the creation of a signal by cryptochrome pigments and the reduction of gibberellin production, resulting in the reduction of stem height. While in some other species, the increase in the production of gibberellin and the increase in height occur in this process 39,40 . It has been reported that there is a close relationship between potassium and the growth of meristem tissues, and the strengthening effect of this element on plant growth regulators biosynthesis such as gibberellin and auxin which leads to the increased cell length and therefore, longitudinal growth of plant organs 41 . In a similar study, AM El-Naggar and B El-Nasharty 42 reported that the use of foliar spraying of 2% potassium along with the soil application of 100% potassium had the most significant effects in plant height, number of leaves per plant, fresh and dry weight of leaves, number of flowers per spike, floret diameter, spike length, fresh and dry weight of florets, new corm diameter, fresh weight, and number of corms per plant in gladiolus.
During various studies, it has been reported that the wavelength range of 640-670 nm (red light) was effective in promoting photosynthetic activity, plant biomass and leaf growth. It also plays a substantial role in the development of the photosynthetic apparatus, the net rate of photosynthesis and primary metabolism 43,44 .
Opening of stomata occurs in response to low concentrations of internal carbon dioxide, high light intensity and high humidity 45 . In low availability of potassium, plants are more susceptible to wilting, and mild potassium deficiency affects photosynthesis rate by reducing stomatal conductance and photosynthetic biochemical reactions 46 . The application of 2.5 g/l nanopotassium fertilizer led to an increase in the stomatal conductance and stem diameter in pumpkin plants (Cucurbita pepo) 47 . In another study, using of potassium sulfate led to an increase in the fresh and dry weight, plant height, root length and leaf area of the Indian mustard (Brassica juncea L.) 48 . www.nature.com/scientificreports/ Potassium is a macro-nutrient, which plays a crucial role in many plant physiological processes such as in cell turgidity and expansion, osmoregulation, stomatal opening and closure, and also works as an activator for several enzymes 49 . It seems that in this way, it has led to an increase in stomatal conductance in the present study. Similar to the present study, in a research, red LED light increased fresh and dry weight of aerial parts, number of stems, leaves and stem height in lemon balm (Melissa officinalis) seedlings compared to blue LED 50 .
Our findings are in confirmation with the results of Ouzounis et al. 51 reported that the total biomass and height of roses was increased with a higher ratio of red to blue light. Findings show that the reaction of plants to specific light spectra's or their different ratios is dependent on species or cultivars. The improving effects of blue and red lights in increasing the growth of plants such as lettuce (Lactuca sativa), radish (Raphanus sativus) and spinach (Spinacia oleracea) 52,53 , petunia 54 and Norway spruce (Picea abies) 55 has been reported. A group of researchers believe that the presence of low intensities of blue light can enhance the activity of pigments such as phototropins and as a result increasing the growrth of plants, but on the other hand, due to the different effects of blue light on other photoreceptors such as cryptochrome and phytochromes, it is possible that the response and reaction of different plant species to growth may different from each other 56,57 . Red light is received by phytochrome and affects the productive biomass and elongation of plants 58 . Blue light also affects photomorphological responses (such as adjusting leaf area and appearance) through phototropins and cryptochromes that act independently or synergistically with phytochrome 59,60 .
Biochemical & photosynthetic traits. The presence of carbohydrates is necessary for flowers development and opening. Carbohydrates causes more water absorption, which increases the cell turgor and the freshness of petals, and therefore, the increase in flowers diameter is expectable 61 . In the present study, the interaction of light and nano-chelated potassium treatment led to an increase in content of photosynthetic pigments (Fig. 3c), and carbohydrates accumulation. Considering the role of carbohydrates in increasing water absorption, it can be expected that the fresh weight of the flower stems will increase.
Chlorophyll and carotenoids, by participation in the light trapping complex, plays a very important role in the efficiency of photosynthesis, light absorption and electron transfer 62 . According to the research conducted by Massa et al. 63 and Niakan et al. 64 , the improving effect of light on growth and chlorophyll content has been emphasized. Red and white lights affects the production of chlorophyll precursors, and increased chlorophyll biosynthesis. Red light irradiation alone was unsuccessful for chlorophyll biosynthesis, while the combination of blue and red light irradiation was necessary for this process and improved chlorophyll biosynthesis and thus photosynthesis rate 65 . The red light of the visible spectrum is needed for the growth of the photosynthetic apparatus and photosynthesis, while the blue light is needed for the synthesis of chlorophyll, chloroplast, stomata opening, and photomorphogenesis 66 . Increasing the amount of photosynthesis in the present study due to red light treatment is likely related to the development of the photosynthetic apparatus. Red light in combination with blue light are best for photosynthesis 10 . Blue light affects stomata width and stomatal conductivity, plant height, and chlorophyll biosynthesis 67 . In confirmation of the results of the present study, Chung et al. 68 reported an increase in the content of chlorophyll in the orchid (Oncidium 'Gower Ramsey) plants exposed to combined red and blue light.
In this study, the use of nano-chelated potassium led to an increase in photosynthetic pigments. Potassium does not have a direct effect on the activity of rubisco carboxylase enzyme, but by increasing the synthesis of carboxylation enzymes such as phosphoenolpyruvate carboxylase (PEP Case), it stimulates the stabilization of carbon dioxide and increases photosynthesis rate 69 . It has been reported that the use of different concentrations of nano-chelated potassium can lead to a significant increase in the amount of chlorophyll a and b, the amount of soluble sugars and protein content in the leaves of plants 70 . In confirmation of the results of the present study, AM El-Naggar and B El-Nasharty 42 reported an increase in the content of chlorophyll a and b in the leaves of the gladiolus plant in response to potassium application. Fig. 3e-f, red light and nano-chelated potassium treatment increased the amount of soluble carbohydrates. Also the amount of total protein and anthocyanin of flowers were affected by the interaction of light and nano-chelated potassium (Fig. 3d,g). Light through the activation of some genes (CHS, CHI & F3H) involved in anthocyanin biosynthesis, causes the accumulation of anthocyanin in green tissues and cultured cells 71 . Researches shows that along with monospectral red light, the combination of blue and red LED spectrum also causes the accumulation of primary metabolites www.nature.com/scientificreports/ as well as the increase of anthocyanins, polyphenols and flavonoids 72,73 . However, red LEDs have a greater effect on anthocyanin accumulation than blue LEDs. This issue may was attributed to the increased expression of anthocyanin biosynthesis genes (for example, MdMYB10 and MdUFGT) due to red light treatment 74 . It has been demonstrated that potassium increases the production of starch and carbohydrates 75 .Chalcone isomerase, one of the key enzymes of anthocyanin biosynthesis can activated by a signal from soluble carbohydrates, so the accumulation of carbohydrates can enhance the production of anthocyanins 76 . Results from a research on Prunus × yedoensis 'Somei-yoshino' petals coloring, showed that a combination of blue and red light causes more anthocyanin production than monochromatic blue light, which indicates the correlation between blue and red light receptors 77 . Findings shown that potassium plays an essential role in the construction of polymer compounds in plants. In plants that suffer from potassium deficiency, simple sugars, soluble nitrogen compounds and amino acids are accumulated and the amount of starch and leaf protein is reduced 78 . Potassium participates in the last stage of the protein production process. K + is an activator of dozens of important enzymes, and contributes in protein synthesis, sugar transport, N and C metabolism, and photosynthesis. It plays an important role in crop yield and quality improvement 31,[79][80][81][82][83] . Therefore, it can be assumed that the using of nano-chelated potassium may be a reason for the increase in the protein content.

Anthocyanin, protein, phenolics & flavonoids. According to
In the present study, the application of red light and nano-chelated potassium led to an increase in the antioxidant capacity and the amount of phenolic compounds and flavonoids of petals. A direct relationship has been reported between the antioxidant properties and the amount of phenolic compounds and anthocyanin content in bayberry (Myrica pensylvanica) 84 and blueberries (Vaccinium corymbosum) 85 . Light quality has a significant effect on the accumulation of different metabolites in plants 86 . Flavonoids are involved in many aspects of plant growth and development, including resistance to pathogens, pigment production, protection against UV rays, pollen development, and seed coat development 87 . The increase in the amount of total phenolic compounds due to potassium treatment can be attributed to the increase in the expression of genes involved in the biosynthesis of phenylpropanoids, and especially the increase in the expression of the gene responsible for the biosynthesis of the enzyme phenyl-alanine-ammonialyase (PAL), which is the first enzyme in the phenolic compound's synthesis pathway 88 . Fig. 3h, the interaction of light and nano-chelated potassium led to a twotime increase in the vase life of cut roses. Aging in plants is an oxidative process and includes biochemical, physiological, hormonal and structural changes, which causes the destruction of large molecules such as protein, nucleic acids and lipids 89 . One of the reasons for senescence in plant tissues is the involvement of reactive oxygen species (ROS) including hydrogen peroxide and hydroxyl, which cause the production of free radicals and the destruction of proteins, lipids and nucleic acid, and finally flower senescence 90,91 . Red light increases the total phenol content as well as radical scavenging capacity 92 that slows down the flower aging. Potassium is an essential macronutrient that contributes in many physiological aspects related to osmotic adjustment, maintaining turgor pressure, cell expansion, plasma membrane electric potential balancing, and homeostatic regulation of pH 49 . In the present study, the application of red light and nano-chelated potassium led to the improving of some indices related to flower quality and vase life such as photosynthetic pigments content, antioxidant capacity and phenolic compounds, so it can be expected that the vase life of rose flowers will increase due to the treatment of red light and nano-chelated potassium.

Conclusion
Using of LED lighting and nano-chelated potassium improved morphological and biochemical traits of 'Dolce Vita' rose flower. Red light in combination with nano-chelated potassium increased the photosynthesis rate and biomass of rose plants (Fig. 4). The biochemical traits such as protein content, antioxidant content, total phenolics and flavonoids, also was affected by red light and nano-chelated potassium that led to color enhancement in petals edge and higher marketability values. In addition, the flower vase life was increased notably. In general, it can be concluded that the use of red light and nano-chelated potassium, can be effective in improving the quality of the produced flowers, especially in seasons that plants is experiencing a decrease in light intensity and duration. www.nature.com/scientificreports/