Effects of sodium nitroprusside and potassium silicate on the growth and flowering of Gazania rigens (L.)
محورهای موضوعی : Plant PhysiologyZahra Nasiri 1 , Elham Danaee 2
1 - Department of Horticulture, Garmsar Branch, Islamic Azad University, Garmsar, Iran
2 - Department of Horticulture, Islamic Azad University, Garmsar Branch, Garmsar, Iran
کلید واژه: Sodium nitroprusside, Potassium silicate, Gazania, Flower longevity, carotenoid,
چکیده مقاله :
Gazania, belongs to the family Asteraceae, is widely grown in gardens and other environments. The purpose of this study was to evaluated the effects of sodium nitroprusside and potassium silicate treatments on the growth and flowering of gazania. For these purposes, a completely randomized design was used, with three levels of sodium nitroprusside (SNP) (25, 50 and 100 μM/l), potassium silicate (PS) at the concentration of 25, 50 and 100 mg/l and control. Some important traits such as fresh and dry weight of shoot and root, number of flowers, root volume, longest root length, plant height, cell membrane stability index, petiole carotenoid, leaf chlorophyll, protein, superoxide dismutase (SOD) and peroxidase (POD) enzyme activity and flower longevity. It was observed that plan that shoot fresh/dry weight, flower number, root length, plant height, carotenoid, leaf chlorophyll was increased under 100 mg/l PS treatment. The results suggest that the application of 50 μM/l SNP has favorable effects on the raise root fresh/dry weight, root volume, cell membrane stability index, protein, SOD and POD activity. Over the growth stage, 50 mg/l PS was found to be the best treatment to maintain flower longevity with 7.2 days.
Gazania, belongs to the family Asteraceae, is widely grown in gardens and other environments. The purpose of this study was to evaluated the effects of sodium nitroprusside and potassium silicate treatments on the growth and flowering of gazania. For these purposes, a completely randomized design was used, with three levels of sodium nitroprusside (SNP) (25, 50 and 100 μM/l), potassium silicate (PS) at the concentration of 25, 50 and 100 mg/l and control. Some important traits such as fresh and dry weight of shoot and root, number of flowers, root volume, longest root length, plant height, cell membrane stability index, petiole carotenoid, leaf chlorophyll, protein, superoxide dismutase (SOD) and peroxidase (POD) enzyme activity and flower longevity. It was observed that plan that shoot fresh/dry weight, flower number, root length, plant height, carotenoid, leaf chlorophyll was increased under 100 mg/l PS treatment. The results suggest that the application of 50 μM/l SNP has favorable effects on the raise root fresh/dry weight, root volume, cell membrane stability index, protein, SOD and POD activity. Over the growth stage, 50 mg/l PS was found to be the best treatment to maintain flower longevity with 7.2 days.
Ahmad, P., A.A. Abdel Latef, E.F. Abd_Allah, A. Hashem, M. Sarwat, N.A. Anjum and S. Guce. 2016. Calcium and potassium supplementation enhanced growth, osmolyte secondary metabolite production, and enzymatic antioxidant machinery in cadmium-exposed chickpea (Cicer arietinum L.). Front Plant Science, 7: 513.
Ahmad, P., M.A. AAhanger, P. Alam, M.N. Alyemeni, L. Wijaya, S. Ali and M. Ashraf. 2019. Silicon (Si) supplementation alleviates NaCl toxicity in mung bean [Vigna radiata (L.) Wilczek] through the modifications of physio-biochemical attributes and key antioxidant enzymes. Journal of Plant Growth Regulator, 38: 70–82.
Barros, T.C., R. De Mello Prado, C. Garcia Roque, G. Ribeiro Barzotto and C. Roberto Wassolowski. 2018. Silicon and salicylic acid promote different responses in legume plants. Journal of Plant Nutrition, 41: 2116–2125.
Bradford M.M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Analytical Biochemistry, 72: 248-254.
Chen Y.X., L. Zou, P. Penttinen, Q. Chen, Q.Q. Li, C.Q. Wang and K.W Xu. 2018. Faba bean (Vicia faba L.) nodulating rhizobia in panxi, china, are diverse at species, plant growth promoting ability, and symbiosis related gene levels. Front. Microbiology. 9: 1338.
Chen D. 2016. Silicon-moderated K-deficiency-induced leaf chlorosis by decreasing putrescine accumulation in sorghum. Annual Botany. 118: 305–315.
Chen D. 2016. Silicon moderated the K deficiency by improving the plant-water status in sorghum. Science Reports. 6: 1–14.
Danaee, E. and V. Abdossi. 2020. Effects of silicon and nano-silicon on some morpho-physiological and phytochemical traits of peppermint (Mentha piperita L.) under salinity stress. Iranian Journal of Medicinal and Aromatic Plants Research. 37: 98-112(in Persian)
Danaee, E. and V. Abdossi. 2020. The effects of drought stress and sodium nitroprusside on growth indices and enzymatic activity of Satureja hortensis. Plant Research Journal (Iranian Biology Journal), 35: (in Persian)
Dallagnola, L.J., F.A. Rodriguesb, F.A. O. Tanakaa, L. Amorima, L.E.A and H. Camargo. 2012. Effect of potassium silicate on epidemic components of powdery mildew on melon. Plant Pathology, 61: 323–330.
Denton, M.D., Pearce D.J, Peoples M.B. 2012. Nitrogen contributions from faba bean (Vicia faba L.) reliant on soil rhizobia or inoculation. Plants Soil, 365: 363–374.
de Souza Junior, JP. 2021. Effect of different foliar silicon sources on cotton plants. Journal of Soil Science Plant Nutriation, 21: 95–103.
Doncheva, SN. 2009. Silicon amelioration of manganese toxicity in Mn-sensitive and Mn-tolerant maize varieties. Environmental Experiment Botany, 65: 189–197.
dos Santos Sarah, M.M. 2021. Silicon supplied via roots or leaves relieves potassium deficiency in maize plants. Silicon, 13: 1–10.
Ezhilmathi, K., V. Singh, P. Arora and R.K. Sairam. 2007. Effect of 5-sulfocalicylic acid on antioxidant in relation to vase life of gladiolus cut flower. Plant Growth Regulation. 51: 99-108.
Giannopolitis, C.N. and S.K., Ries. 1997. Superoxide Dismutases II. Purification and quantitative relationship with water-soluble protein in seedlings. Plant Physiology, 59: 315–318.
Gomaa, M.A., E.E. Kandil, A.A.M.Z. El-Dein, M.E.M. Abou-Donia, H.M. Ali and Abdelsalam N.R. 2021. Increase maize productivity and water use efficiency through application of potassium silicate under water stress. Science Reports, 11: 224
Habermann. E. 2021. How does leaf physiological acclimation impact forage production and quality of a warmed managed pasture of Stylosanthes capitata under different conditions of soil water availability? Science Total Environment. 759: 238–244.
Hafez, E.M., H.S. Osman., S. M. Gowayed., S.A. Okasha, A.E.D, Omara, R. Sami, Abd A. M. El-Monem and U. A. Abd El-Razek. 2021. Minimizing the adversely impacts of water deficit and soil salinity on maize growth and productivity in response to the application of plant growth-promoting rhizobacteria and silica nanoparticles. Agronomy. 11: 676.
Hasanuzzaman, M., M.H.M.B. Bhuyan, K. Nahar, S. Hossain, J. Al Mahmud, S. Hossen, A.A.C. Masud, M. Moumita and M. Fujita. 2018. Potassium: A vital regulator of plant responses and tolerance to abiotic stresses. Agronomy. 8, 31.
Hosseinzadeh Rostam Kalaei, M., V. Abdossi and E. Danaee. 2022. Evaluation of foliar application of selenium and fowering stages on selected properties of Iranian Borage as a medicinal plan. Scientifc Reports. 12: 1-10.
Kamenidou, S., T.J. Cavins and S. Marek. 2008. Silicon supplements affect horticultural traits of greenhouse-produced ornamental sunflowers. Horticultural Science. 43:236–239.
Kamenidou, S., T.J. Cavins and S. Marek. 2009. Evaluation of silicon as a nutritional supplement for greenhouse zinnia production. Scientia Horticultrae. 119:297–301.
Khalil, M.M.N. 2019. Effect of mineral fertilizers and biofertilization on some soil properties and faba bean productivity under saline soil conditions. Journal of Soil Science and Agricultural Engineering. 10: 889–897.
Liang, Y., Q. Chen, Q. Liu, W. Zhang and R. Ding. 2003. Exogenous silicon (Si) increases antioxidant enzyme activity and reduces lipid peroxidation in roots of salt-stressed barley (Hordeum vulgare L.). Journal of Plant Physiology, 160: 1157–1164.
Lichtenthaler H.K. 1987. Plant cell membranes. Methods in Enzymology. 148: 48036–48041
Ma, J.F. 2004. Role of silicon in enhancing the resistance of plants to biotic and abiotic stresses. Soil Science Plant Nutrition, 50:11–18.
Machado, R.M. and R.P. Serralheiro. 2017. Soil salinity: Effect on vegetable crop growth. Management practices to prevent and mitigate soil salinization. Horticulturae. 3, 30.
Maghsoudi, K., Y. Emam and M. Pessarakli. 2016. Effect of silicon on photosynthetic gas exchange, photosynthetic pigments, cell membrane stability and relative water content of different wheat cultivars under drought stress conditions. Journal of Plant Nutrition. 39: 1001–1015.
Miao B.H., X. G. Han and W.H. Zhang. 2010. The ameliorative effect of silicon on soybean seedlings grown in potassium-deficient medium. Annual Botany. 2010. 105: 967–973.
Mostofi Y. and F. Najafi. 2005. Analytical laboratory methods in horticultural sciences. University of Tehran Press. 136 p
Nabi, R.B.S., R. Tayade R, A. Hussain, K.P. Kulkarni, Q.M. Imran, B.G. Mun, B.W. Yun. 2019. Nitric oxide regulates plant responses to drought, salinity, and heavy metal stress. Environmental Experience in Botany. 161: 120–133.
Nadeem, M., J. Li, M. Yahya., M. Wang, A. Ali, A. Cheng, X. Wang and C. Ma. 2019. Grain legumes and fear of salt stress: Focus on mechanisms and management strategies. International Journal of Molecular Science. 20: 799.
Naing, A.H., K. Lee, M. Arun, K.B. Lim and C.K. Kim. 2017. Characterization of the role of sodium nitroprusside (SNP) involved in long vase life of different carnation cultivars. BMC Plant Biology. 17:149.
Neil, S., L. Mattson and W. Roland Leatherwood. 2010. Potassium Silicate Drenches Increase Leaf Silicon Content and Affect Morphological Traits of Several Floriculture Crops Grown in Peat-based Substrate. Horticultural Science. 45:43–47.
Pagnussat G. C., M. L. Lanteri, M. C. Lombardo and L Lamattina. 2004. Nitric oxide mediates the indole acetic acid induction activation of a mitogen-activated protein kinase cascade involved in adventitious root development. Plant Physiol. 135:279–286
Pessarakli, M. and I. Szabolcs. 2010. Soil Salinity and Sodicity as Particular Plant/Crop Stress Factors. In Handbook of Plant and Crop Stress, 3rd ed.; CRC Press: Boca Raton, FL, USA. pp. 3–21
Polle, A., T. Otter and F. Seifert. 1994. Apoplastic peroxidases and lignification in needles of Norway spruce (Picea abies L.). Plant Physiology, 106: 53-60
Qadir, M., A.S. Qureshi and S. A. M. Cheraghi. 2008. Extent and characterisation of salt-affected soils in Iran and strategies for their amelioration and management. Land Degradation & Development. 19: 214–227.
Rodrigues, F.A., H.S.S. Duarte, G.P. Domiciano, C.A. Souza, G.H. Korndörfer and L. Zambolim. 2009. Foliar application of potassium silicate reduces the intensity of soybean rust. Australas. Plant Pathology. 38: 366–372.
Singh, A., J. Kumar and P. Kumar. 2008. Effect of plant growth regulators and sucrose on post-harvest physiology, membrane stability and vase life of cut spikes of Gladiolus, Journal of Plant Growth Regulator. 55: 221-229
Soroori, S. and E. Danaee. 2023. Effects of Foliar Application of Citric Acid on Morphological and Phytochemical Traits of Calendula officinalis L. under Drought Stress Conditions. International Journal of Horticultural Science and Technology. 10: 361-374
Yaghubi, K., N. Ghaderi, Y. Vafaee and T. Javadi. 2016. Potassium silicate alleviates deleterious effects of salinity on two strawberry cultivars grown under soilless pot culture. Scientia Horticulture. 2213: 87–95.
Youssef Moustafa, A.M., A. Ismail Khodair and F.M. Hammouda. 2007. Phytochemical investigation and α-cellulose content determination of Gazania splendens Moore. Research Journal of Phytochemistry. 1: 21-32.
1405
Zahra Nasiri and Elham Danaee*
Department of Horticulture, Islamic Azad University, Garmsar Branch, Garmsar, Iran
________________________________________________________________________________
Abstract
Gazania, belonging to the family Asteraceae, is widely grown in gardens and other environments. The purpose of this study was to evaluated the effects of sodium nitroprusside and potassium silicate treatments on the growth and flowering of gazania. For this purpose, a completely randomized design was used with three levels of sodium nitroprusside (SNP) (25, 50, and 100 μM/l) and three levels of potassium silicate (PS) (25, 50, and 100 mg/l) and control. Traits under investigation included fresh and dry weight of shoot and root, number of flowers, root volume, longest root length, plant height, cell membrane stability index, petiole carotenoid, leaf chlorophyll, protein, superoxide dismutase (SOD) and peroxidase (POD) enzyme activity, and flower longevity. It was observed that shoot fresh/dry weight, flower number, root length, plant height, carotenoid, and leaf chlorophyll increased under 100 mg/l PS treatment. The results suggest that the application of 50 μM/l SNP has favorable effects on root fresh/dry weights, root volume, cell membrane stability index, protein, SOD and POD activity. Over the growth stage, 50 mg/l PS was found to be the best treatment to maintain flower longevity with 7.2 days.
Keywords: sodium nitroprusside, potassium silicate, Gazania, flower longevity, carotenoid
Nasiri, Z., E. Danaee. 2023. 'Effects of sodium nitroprusside and potassium silicate on the growth and flowering of Gazania rigens (L.)'. Iranian Journal of Plant Physiology 14 (1), 4833-4841.
|
_____________________________________ * Corresponding Author E-mail Address: dr.edanaee@yahoo.com Received: June, 2023 Accepted: December, 2023
|
Salinity is a major problem affecting crop production all over the world. In fact, 20% of cultivated land in the world and 33% of irrigated land are salt-affected and degraded (Machado and Serralheiro, 2017). In arid and semi-arid regions, several interrelated factors could restrain sustainable agricultural development, including a lack of fresh irrigation water, soil salinity, and an increase in evapotranspiration (Qadir et al., 2008). The salt content in the soil adversely impacts soil productivity which limits the growth and ruined plant performance (Pessarakli and Szabolcs, 2010). According to Machado and Serralheiro (2017), increment levels of soil salinity are attributed to the irrigation of crops with saline water.
Foliar spraying on plants to promote growth and lessen the negative effects of salt stress is a useful advancement towards a replacement technique in agriculture (Gomaa et al., 2021). Along with serving as a source of potassium (K) and more soluble silicon (Si) than other fertilizers, potassium silicate (K2 SiO3) is used in plants (Rodrigues et al., 2009). Silicate can develop root structure, plant improvement, leaf firmness, photosynthesis, and water contents. It also can be regarded as one of the most remarkable factors in plant productivity, principally in reducing the adverse effects of salt and oxidative stress (Liang et al., 2003). Potassium (K) is a primary macronutrient for overall plant growth, yield potential, product quality, and stress resistance of plants (Hasanuzzaman et al., 2018). It can be applied to decrease the adverse impact of salt tension in plants. Potassium silicate (PS) could develop yield-linked properties and quality and element (N, P, K) uptake (Gomaa et al. 2021). Hafez et al., (2021) indicated that the use of K2 SiO3 under the saline water irrigation treatment had the capability to reduce the levels of exchangeable sodium percentage (ESP) in the soil.
Nitric oxide (NO) is an endogenous signaling molecule that plays an important role in plant ontogenesis and responses to different stresses (Doncheva et al., 2009). Utilizing exogenous chemical donors such as sodium nitroprusside (SNP) is one of the most popular ways to examine the effects of nitric oxide on plants (Denton et al., 2012). Nitric oxide also impacts lignification and sodium nitroprusside was shown to ameliorate the vase life of different flowers, including Rosa sp., Gladiolus communis, and Dianthus caryophyllus by decreasing ethylene synthesis and senescence-related genes and by increasing antioxidant activity (Naing et al., 2017). Also, it has beneficial effect in terms of recovery from salinity, drought etc. Accordingly, the exogenous application of NO may result in an enhanced crop yield under adverse conditions owing to its role in regulating mechanisms related to increased tolerance to abiotic stress (Nabi et al., 2019). Mirakhorli et al (2021) observed that NO fertilization may operate particular signaling cascades, therewith boosting the growth, efficiency, and immunity system of plants. Besides, they indicated that the foliar application technique was more useful than the soil solution.
Since source and concentration have an impact on the rate at which this element polymerizes in solution, they both affect the optimum foliar uptake of K. and the plant reaction. In fact, there are concerns about the best K source and dosage for foliar spraying in garden and bedding plants. Previous studies on container-grown floriculture crops have either focused on a small number of species or have been conducted in hydroponics with purified water. However, there has only been limited research on plants grown in soil media. The use of Si, K, and NO in commercial gazania culture has not been tested, and as a result, there has been a very slow pace of research. Therefore, the aim of this study was to investigate if foliar application of potassium silicate and sodium nitroprusside will change the enzyme activity or affect the morphological and physiological characteristics of gazania.
Materials and Methods
Plant material and treatment
This study was performed in a commercial greenhouse under 22-23 ℃, relative humidity of 50-60%, and light intensity of 60-70 µM/m2/sec. Seeds with suitable germination qualities were supplied from the seed bank of the Institute of Medicinal Plants. Six plants were kept in each pot after thinning out from each cultivation of twenty seeds. During the growth season, other activities were regularly carried out. The experiment was arranged in a completely randomized design with 6 treatments and 3 replications (CRD). The treatments consisted of SNP at three levels of 25, 50, and 100 Μm, PS at three concentrations of 25, 50, and 100 mg/l and control (plants sprayed with water). For foliar application, treatments were applied after emerging flower bud, as a fine mist on the upper surface of the leaves followed by four times spraying during growth season with 3-day intervals (Dallagnol et al., 2012).
Evaluation of traits was performed about 10 days after the last foliar application. Samples were placed in nylon bags and sent to the lab. Evaluated characteristics included plant height, number of flowers, fresh and dry weight of shoots and roots, cell membrane stability index, petiole carotenoid content, total leaf chlorophyll, protein content, SOD and POD activity, and flower longevity.
Quality attributes
Fresh weight of fresh plant was recorded, using a digital scale with an accuracy of 0.01. Weight loss was estimated in each replication and was noted initially and after 15, 30, and 45 days during storage. The longest root length and plant height were measured with a ruler. Samples of both roots and shoots were weighed by a digital scale with an accuracy of 0.01 after being dried for 72 hours around 60 ℃ (Hosseinzadeh Rostam Kalaei et al., 2022). The root volume of each plant was recorded by a calibrated stone after washing the roots. Also, the number of flowers in each pot was counted. Flower longevity on the plant from the time of flower opening and the appearance of color to wilting, paleness, and shedding of flowers was calculated and expressed as the day (Ezhilmathi, 2007).
Nitro blue Tetrazolium (NBT) approach was used to test the SOD activity. Liquid nitrogen was used to grind the 200 mg samples, which were then homogenized using phosphate buffer (pH 7.0) and 0.5 mM EDTA. It was then centrifuged in a rotor for 15 minutes at 4 ℃ at 18,000 rpm. To evaluate the SOD activity, 1500 ml of phosphate buffer (50 mM), 300 ml of sodium carbonate (50 mM), 300 ml of methionine (12 mM), 300 ml of nitro blue tetrazolium chloride (75 mM), 300 l of riboflavin (1 mM), and 300 l of the enzyme extract were utilized. The sample's absorbance at 560 nm was measured using a spectrophotometer. The decrease of NBT is 50% inhibited by one unit of SOD enzyme activity (Giannopolitis and Ries, 1997). POD was assayed following the procedure outlined by Polle et al. (1994). The carotenoid content was obtained using fruit ground with 5% of 80% acetone. The extract was then poured into a falcon and refrigerated for 4 hours at 4 ℃. The absorption was noted by the spectrophotometer at 480 and 510 nm (Mostofi and Najafi, 2005).
The amount of protein was determined by Bradford (1976) method by extracting a protein extract of 0.05 g from plant dry matter and adding 4 ml of tris hydrochloric acid buffer to it. The samples were mixed with a vortex shaker for 20 min. After that, they received a 30 min centrifugation at a speed of 5000 rpm and the upper phase containing the total protein was separated. Then, 5 ml of Bradford solution was added to 0.1 ml of protein extract from each sample and then vortexed for 20 min and the adsorption was recorded at 595 nm.
The chlorophyll content was estimated according method of Soroori and Danaee (2023). Total chlorophyll content was measured by the spectrophotometer at wavelengths of 663 and 645 nm, and was expressed as mg g-1 FW leaves.
For determination of electrolytic conductivity, the samples were placed at a water bath in 30 ℃ for 60 min; then, the EC1 level was recorded by an EC meter. The falcons were then transferred to an autoclave at 120 ℃ for 20 min at 1.2 atm. After cooling, the EC2 was recorded. Finally, cell membrane stability index was expressed as percentage (Singh et al., 2008).
Statistical Analysis
SPSS software was used for the statistical analysis of the data. Data values were compared using LSD test at 1% and 5% probability levels.
Results
PS and SNP affected shoot fresh and dry weights, root fresh weight, cell membrane stability index, plant height, carotenoid, anthocyanin content, chlorophyll, SOD, POD, and flower longevity (P≥0.05). In this experiment, protein, root dry weight, and root length of plants sprayed with PS and SNP were significantly (P≥0.01) different from control (Table 1).
Analysis of variance of application of sodium nitroprusside coupled with potassium silicate on the growth and flowering traits of Gazania rigens (L.)
ns, *, and ** indicate non-significant and significant at P≤0.05 and P≤0.01, respectively.
Effect of application of sodium nitroprusside coupled with potassium silicate on the growth and flowering traits of Gazania rigens (L.)
Data are means ± standard error (n=3); the means followed by the same letter are not different according to the LSD test. Potassium Silicate: PS; Sodium nitroprusside (SNP)
|
Discussion
Potassium silicate reduces water consumption, improves drought tolerance, and enhances the productivity under deficit irrigation (Ma et al., 2004). In our study, PS treatment reduced foliar transpiration and increased shoot and root fresh weight. This is because of the regulation of a silica gel layer that attaches cellulose to epidermal cells, decreasing water loss, and subsequently the increment activity of aquaporin, a protein linked to the gained water transportation in plants (Chen, 2016). The advantages of Si in raising the performance of water utilization in a K-deprived plant are significance. This is because climate change has induced prolonged droughts in crops, restricting water availability and harming the physiological aspects of the crop (Habermann 2021). A same effect of enhanced dry matter in K-deficient plants treated with silicon through nutrient solution was reported in some species including Glycine max and Sorghum bicolor (Ma et al., 2004; Miao et al., 2021). The incremented dry weight effects on Bracteantha bracteatum, Lobelia spp., and Verbena officinalis with silicon nutrient are considerable and require further research (Neil et al., 2010). Potassium has promoted root length, vegetative growth, and osmoregulation (Hasanuzzaman et al., 2018).
The plants treated with 100 ppm PS showed maximum height (24.41 cm) compared to control. Substrate-incorporated PS supplement led to maximum stem height of Zinnia elegans although weekly application of high concentration of PS delayed anthesis and decreased shoot length in zinnia and Helianthus annuus and was coupled with disordered flowers (Neil et al., 2010). These results agreed with Danaee and Abdossi (2020) who indicated that different levels of silicon and nano-silicon improved the plan growth.
Significant difference was found in cell membrane index for 50 ppm PS which was still higher after growth period. This is in line with Miao et al. (2010) studying Glycine max plants that took silicon through nutrient supplement. The efficacy of silicon in decreasing electrolyte leakage is because of its ability to induce greater plasma membrane protection.
SOD activity was affected by 50 µM SNP since this treatment resulted in 46.76 Unit enzyme/g FW during growth time. Moreover, 50 ppm PS with 132.57 Unit enzyme/g FW reinforced POD activity. Ahmad et al. (2016) showed that potassium improved ionic equivalency and antioxidant enzyme activity. PS has a positive impact on plant growth, productivity, and performance (Hafez et al., 2021). Consequently, increasing the functioning of enzyme-mediated antioxidants along with salt content tension sustains plasma-membrane activity, e.g., through regulating the penetrance, which is associated with maximum root activities, improving the root's ability to accumulate vital nutrients (Ahmad et al., 2019). NO, a form of reactive nitrogen species (RNS), can limit the negative effects of reactive oxygen species (ROS) by acting as a network splitter and by increasing the gene synthesis of antioxidant enzymes (Nadeem et al., 2019). The research strongly supports the idea that NO, which is a medium for enhancing plant resistance to abiotic stress, is linked to a significant ROS detoxification by defense mechanisms. NO plays a role in expanding the antioxidant chain in plants. Additionally, NO has been shown to possess antioxidant properties, playing a role in the reactive oxygen species detoxifying process and therefore helping to prevent lipid peroxidation and oxidative damage to proteins (Chen et al., 2018). In spite of the fact that the role of NO is relatively well-understood in drought conditions, salinity, and heavy metal contamination (Khalil, 2019), its collaboration in herbicide-induced phytotoxicity, such as glyphosate, remains inexpertly investigated.
Carotenoid content was significantly greater in 100 ppm PS than the other treatments (0.894 mg/g FW). Chlorophyll level of gazania leaves significantly increased to 9.543 mg/g FW under 50 ppm PS treatment. Treatment of 50 ppm PS with 3.89 µg/mg FW, demonstrated maximum protein content. Silicon increases the plant prospective by decreasing sodium ion uptake and enhancing potassium ion absorption in the leaves (Yaghubi et al., 2016). Potassium has been presented to boost physiological activities including chlorophyll pigments, stomata movement, and water condition (Hasanuzzaman et al., 2018). Si reduces oxidative damage to cells and enhance a certain amount of chlorophyll, and free of enzymes antioxidants component like carotenoids. These silicon properties boost levels of activity in photosynthesis (Chen, 2016), decrement transpiration and raising water usage performance, and consequently potassium-deficient plants produce less dry matter (Ma, 2004; Mia et al., 2010; Chen, 2016; dos Santos Sarah, 2021). Barros et al. (2018) found the same result in Phaseolus vulgaris L. after foliar applying of Si. Accumulation of silicon in hydroponically-grown bean crops sprayed with silicon barricaded pigment destruction. This shows the impact of silicon on leaf epidermis, which defends the photosynthetic tissues. Souza Junior et al. (2021) evaluated the principal efficacy of controlling silicate sources similar to the one used in the present study compared to the PS, and reported enhancement in accumulation of silicon, the percentage of chlorophyll, photosystem II performance, and therefore the dry matter efficiency of Gossypium herbaceum L. This development in pigments boosted by silicon improves the rate of photosynthesis via expanding electrons transportation and activating the genes connected with photosynthesis as well as Rubisco enzyme (Maghsoudi et al., 2016). Carotenoid acts as a non-enzymatic antioxidant that eliminates singlet oxygen (O-2), a primarily harmful ROS, which causes lipid peroxidation, destruction of electrolytes inside of cells, and resistance of the lipid bilayer membrane. Additionally, since silicon functions as an attachment in light absorption for photosynthesis and protects the amount of chlorophyll from photooxidation in the reaction focus, the rise in carotenoids affected by its treatment is crucial for the stabilization in the photosynthetic system (Lichtenthaler, 1987). Improved enzymatic activity in plants treated with different levels of sodium nitroprusside as found in the present study agrees with the findings of Danaee and Abdossi (2020).
The maximum flower number was observed under 50 µM SNP treatment. Also, 50 ppm PS with 7.2 days resulted in the flowers with the longest life while control treatment with 3.8 days lasted the for the shortest time. SNP is one of the most extensively studied NO donors. In the present study, we found that SNP enhanced number of flowers. Our results are in line with Pagnussat et al. (2004), who found that NO is involved in the auxin response throughout the adventitious rooting procedure in Cucumis sativus via activating protein kinase cascades in response to certain mitogens. The favorable morphological effects of silicon are similar to the findings reported by other researchers e.g., Kamenidou et al. (2008, 2009), who reported that silicon content and form have a major impact on plants’ morphology.
Conclusion
In sum, foliar spraying of PS enhanced the total chlorophyll and the amount of antioxidant carotenoid compounds while decreasing the amount of electrolyte leakage, all of which favored the rate of photosynthesis. Therefore, form and concentration of applied silicon significantly impacts on flower longevity life. On the other hand, SNP increased flower number, and gazania plants can all benefit from PS and SNP supplementation.
References
Ahmad, P., A.A. Abdel Latef, E.F. Abd_Allah, A. Hashem, M. Sarwat, N.A. Anjum and S. Guce. 2016. Calcium and potassium supplementation enhanced growth, osmolyte secondary metabolite production, and enzymatic antioxidant machinery in cadmium-exposed chickpea (Cicer arietinum L.). Front Plant Science, 7: 513.
Ahmad, P., M.A. AAhanger, P. Alam, M.N. Alyemeni, L. Wijaya, S. Ali and M. Ashraf. 2019. Silicon (Si) supplementation alleviates NaCl toxicity in mung bean [Vigna radiata (L.) Wilczek] through the modifications of physio-biochemical attributes and key antioxidant enzymes. Journal of Plant Growth Regulator, 38: 70–82.
Barros, T.C., R. De Mello Prado, C. Garcia Roque, G. Ribeiro Barzotto and C. Roberto Wassolowski. 2018. Silicon and salicylic acid promote different responses in legume plants. Journal of Plant Nutrition, 41: 2116–2125.
Bradford M.M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Analytical Biochemistry, 72: 248-254.
Chen Y.X., L. Zou, P. Penttinen, Q. Chen, Q.Q. Li, C.Q. Wang and K.W Xu. 2018. Faba bean (Vicia faba L.) nodulating rhizobia in panxi, china, are diverse at species, plant growth promoting ability, and symbiosis related gene levels. Front. Microbiology. 9: 1338.
Chen D. 2016. Silicon-moderated K-deficiency-induced leaf chlorosis by decreasing putrescine accumulation in sorghum. Annual Botany. 118: 305–315.
Chen D. 2016. Silicon moderated the K deficiency by improving the plant-water status in sorghum. Science Reports. 6: 1–14.
Danaee, E. and V. Abdossi. 2020. Effects of silicon and nano-silicon on some morpho-physiological and phytochemical traits of peppermint (Mentha piperita L.) under salinity stress. Iranian Journal of Medicinal and Aromatic Plants Research. 37: 98-112(in Persian)
Danaee, E. and V. Abdossi. 2020. The effects of drought stress and sodium nitroprusside on growth indices and enzymatic activity of Satureja hortensis. Plant Research Journal (Iranian Biology Journal), 35: (in Persian)
Dallagnola, L.J., F.A. Rodriguesb, F.A. O. Tanakaa, L. Amorima, L.E.A and H. Camargo. 2012. Effect of potassium silicate on epidemic components of powdery mildew on melon. Plant Pathology, 61: 323–330.
Denton, M.D., Pearce D.J, Peoples M.B. 2012. Nitrogen contributions from faba bean (Vicia faba L.) reliant on soil rhizobia or inoculation. Plants Soil, 365: 363–374.
de Souza Junior, JP. 2021. Effect of different foliar silicon sources on cotton plants. Journal of Soil Science Plant Nutriation, 21: 95–103.
Doncheva, SN. 2009. Silicon amelioration of manganese toxicity in Mn-sensitive and Mn-tolerant maize varieties. Environmental Experiment Botany, 65: 189–197.
dos Santos Sarah, M.M. 2021. Silicon supplied via roots or leaves relieves potassium deficiency in maize plants. Silicon, 13: 1–10.
Ezhilmathi, K., V. Singh, P. Arora and R.K. Sairam. 2007. Effect of 5-sulfocalicylic acid on antioxidant in relation to vase life of gladiolus cut flower. Plant Growth Regulation. 51: 99-108.
Giannopolitis, C.N. and S.K., Ries. 1997. Superoxide Dismutases II. Purification and quantitative relationship with water-soluble protein in seedlings. Plant Physiology, 59: 315–318.
Gomaa, M.A., E.E. Kandil, A.A.M.Z. El-Dein, M.E.M. Abou-Donia, H.M. Ali and Abdelsalam N.R. 2021. Increase maize productivity and water use efficiency through application of potassium silicate under water stress. Science Reports, 11: 224
Habermann. E. 2021. How does leaf physiological acclimation impact forage production and quality of a warmed managed pasture of Stylosanthes capitata under different conditions of soil water availability? Science Total Environment. 759: 238–244.
Hafez, E.M., H.S. Osman., S. M. Gowayed., S.A. Okasha, A.E.D, Omara, R. Sami, Abd A. M. El-Monem and U. A. Abd El-Razek. 2021. Minimizing the adversely impacts of water deficit and soil salinity on maize growth and productivity in response to the application of plant growth-promoting rhizobacteria and silica nanoparticles. Agronomy. 11: 676.
Hasanuzzaman, M., M.H.M.B. Bhuyan, K. Nahar, S. Hossain, J. Al Mahmud, S. Hossen, A.A.C. Masud, M. Moumita and M. Fujita. 2018. Potassium: A vital regulator of plant responses and tolerance to abiotic stresses. Agronomy. 8, 31.
Hosseinzadeh Rostam Kalaei, M., V. Abdossi and E. Danaee. 2022. Evaluation of foliar application of selenium and fowering stages on selected properties of Iranian Borage as a medicinal plan. Scientifc Reports. 12: 1-10.
Kamenidou, S., T.J. Cavins and S. Marek. 2008. Silicon supplements affect horticultural traits of greenhouse-produced ornamental sunflowers. Horticultural Science. 43:236–239.
Kamenidou, S., T.J. Cavins and S. Marek. 2009. Evaluation of silicon as a nutritional supplement for greenhouse zinnia production. Scientia Horticultrae. 119:297–301.
Khalil, M.M.N. 2019. Effect of mineral fertilizers and biofertilization on some soil properties and faba bean productivity under saline soil conditions. Journal of Soil Science and Agricultural Engineering. 10: 889–897.
Liang, Y., Q. Chen, Q. Liu, W. Zhang and R. Ding. 2003. Exogenous silicon (Si) increases antioxidant enzyme activity and reduces lipid peroxidation in roots of salt-stressed barley (Hordeum vulgare L.). Journal of Plant Physiology, 160: 1157–1164.
Lichtenthaler H.K. 1987. Plant cell membranes. Methods in Enzymology. 148: 48036–48041
Ma, J.F. 2004. Role of silicon in enhancing the resistance of plants to biotic and abiotic stresses. Soil Science Plant Nutrition, 50:11–18.
Machado, R.M. and R.P. Serralheiro. 2017. Soil salinity: Effect on vegetable crop growth. Management practices to prevent and mitigate soil salinization. Horticulturae. 3, 30.
Maghsoudi, K., Y. Emam and M. Pessarakli. 2016. Effect of silicon on photosynthetic gas exchange, photosynthetic pigments, cell membrane stability and relative water content of different wheat cultivars under drought stress conditions. Journal of Plant Nutrition. 39: 1001–1015.
Miao B.H., X. G. Han and W.H. Zhang. 2010. The ameliorative effect of silicon on soybean seedlings grown in potassium-deficient medium. Annual Botany. 2010. 105: 967–973.
Mostofi Y. and F. Najafi. 2005. Analytical laboratory methods in horticultural sciences. University of Tehran Press. 136 p
Nabi, R.B.S., R. Tayade R, A. Hussain, K.P. Kulkarni, Q.M. Imran, B.G. Mun, B.W. Yun. 2019. Nitric oxide regulates plant responses to drought, salinity, and heavy metal stress. Environmental Experience in Botany. 161: 120–133.
Nadeem, M., J. Li, M. Yahya., M. Wang, A. Ali, A. Cheng, X. Wang and C. Ma. 2019. Grain legumes and fear of salt stress: Focus on mechanisms and management strategies. International Journal of Molecular Science. 20: 799.
Naing, A.H., K. Lee, M. Arun, K.B. Lim and C.K. Kim. 2017. Characterization of the role of sodium nitroprusside (SNP) involved in long vase life of different carnation cultivars. BMC Plant Biology. 17:149.
Neil, S., L. Mattson and W. Roland Leatherwood. 2010. Potassium Silicate Drenches Increase Leaf Silicon Content and Affect Morphological Traits of Several Floriculture Crops Grown in Peat-based Substrate. Horticultural Science. 45:43–47.
Pagnussat G. C., M. L. Lanteri, M. C. Lombardo and L Lamattina. 2004. Nitric oxide mediates the indole acetic acid induction activation of a mitogen-activated protein kinase cascade involved in adventitious root development. Plant Physiol. 135:279–286
Pessarakli, M. and I. Szabolcs. 2010. Soil Salinity and Sodicity as Particular Plant/Crop Stress Factors. In Handbook of Plant and Crop Stress, 3rd ed.; CRC Press: Boca Raton, FL, USA. pp. 3–21
Polle, A., T. Otter and F. Seifert. 1994. Apoplastic peroxidases and lignification in needles of Norway spruce (Picea abies L.). Plant Physiology, 106: 53-60
Qadir, M., A.S. Qureshi and S. A. M. Cheraghi. 2008. Extent and characterisation of salt-affected soils in Iran and strategies for their amelioration and management. Land Degradation & Development. 19: 214–227.
Rodrigues, F.A., H.S.S. Duarte, G.P. Domiciano, C.A. Souza, G.H. Korndörfer and L. Zambolim. 2009. Foliar application of potassium silicate reduces the intensity of soybean rust. Australas. Plant Pathology. 38: 366–372.
Singh, A., J. Kumar and P. Kumar. 2008. Effect of plant growth regulators and sucrose on post-harvest physiology, membrane stability and vase life of cut spikes of Gladiolus, Journal of Plant Growth Regulator. 55: 221-229
Soroori, S. and E. Danaee. 2023. Effects of Foliar Application of Citric Acid on Morphological and Phytochemical Traits of Calendula officinalis L. under Drought Stress Conditions. International Journal of Horticultural Science and Technology. 10: 361-374
Yaghubi, K., N. Ghaderi, Y. Vafaee and T. Javadi. 2016. Potassium silicate alleviates deleterious effects of salinity on two strawberry cultivars grown under soilless pot culture. Scientia Horticulture. 2213: 87–95.
Youssef Moustafa, A.M., A. Ismail Khodair and F.M. Hammouda. 2007. Phytochemical investigation and α-cellulose content determination of Gazania splendens Moore. Research Journal of Phytochemistry. 1: 21-32.