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Article

Exogenous Gibberellic Acid or Dilute Bee Honey Boosts Drought Stress Tolerance in Vicia faba by Rebalancing Osmoprotectants, Antioxidants, Nutrients, and Phytohormones

by
Mostafa M. Rady
1,*,
Sara H. K. Boriek
1,
Taia A. Abd El-Mageed
2,
Mohamed A. Seif El-Yazal
1,
Esmat F. Ali
3,
Fahmy A. S. Hassan
3 and
Abdelsattar Abdelkhalik
4,*
1
Botany Department, Faculty of Agriculture, Fayoum University, Fayoum 63514, Egypt
2
Soil and Water Science Department, Faculty of Agriculture, Fayoum University, Fayoum 63514, Egypt
3
Department of Biology, College of Science, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia
4
Horticulture Department, Faculty of Agriculture, Fayoum University, Fayoum 63514, Egypt
*
Authors to whom correspondence should be addressed.
Plants 2021, 10(4), 748; https://doi.org/10.3390/plants10040748
Submission received: 20 March 2021 / Revised: 6 April 2021 / Accepted: 8 April 2021 / Published: 11 April 2021
(This article belongs to the Special Issue Abiotic Stress Tolerance in Crop and Medical Plants)
Versions Notes

Abstract

:
The use of growth regulators such as gibberellic acid (GA3) and biostimulants, including diluted bee honey (Db-H) can improve drought tolerance in many crops, including the faba bean (Vicia faba L.). Db-H contains high values of osmoprotectants, mineral nutrients, vitamins, and many antioxidants making it an effective growth regulator against environmental stress effects. Therefore, the present study was planned to investigate the potential improvement in the faba bean plant performance (growth and productivity) under full watering (100% of crop evapotranspiration (ETc)) and drought stress (60% of ETc) by foliar application of GA3 (20 mg L−1) or Db-H (20 g L−1). The ameliorative impacts of these growth regulators on growth, productivity, physio-biochemical attributes, nutrient status, antioxidant defense system, and phytohormones were evaluated. GA3 or Db-H attenuated the negative influences of drought stress on cell membrane stability, ion leakage, relative water content, nutrient status, leaf pigments related to photosynthesis (chlorophylls and carotenoids), and efficiency of the photosystem II (PSII in terms of Fv/Fm and performance index), thus improving faba bean growth, green pod yield, and water use efficiency. Drought stress caused an abnormal state of nutrients and photosynthetic machinery due to increased indicators of oxidative stress (malondialdehyde (MDA), hydrogen peroxide (H2O2) and superoxide (O2•−)), associated with increased osmoprotectants (proline, glycine betaine, soluble sugars, and soluble protein), non-enzymatic antioxidants (ascorbic acid, glutathione, and α-tocopherol), and enzymatic antioxidant activities (superoxide dismutase, catalase, glutathione reductase, and ascorbate peroxidase). However, foliar-applied GA3 or Db-H mediated further increases in osmoprotectants, antioxidant capacity, GA3, indole-3-acetic acid, and cytokinins, along with decreased levels of MDA and abscisic acid. These results suggest the use of GA3 or Db-H at the tested concentrations to mitigate drought-induced damage in bean plants to obtain satisfactory growth and productivity under a water deficit of up to 40%.

1. Introduction

Among the most important legume crops, the faba bean (Vicia faba L.) is widely cultivated around the world. Fresh pods and dry seeds are consumed worldwide for humans due to their nutritional value, which is considered among vegetables [1]. Faba bean is rich in protein (up to 35% of dry matter) [2], carbohydrates (51–68% of dry matter) [1], and mineral nutrients such as potassium (K), iron (Fe), calcium (Ca), magnesium (Mg), and zinc (Zn) [2,3].
Limited irrigation water is one of the biggest limiting factors for crop production [4,5], given that irrigated agriculture is the largest user of freshwater, with approximately 79% in Egypt and 69% worldwide of total water withdrawals [6]. Dwindling freshwater resources along with meeting the demand for food production requires increased water use efficiency (WUE) in both irrigated and rainfed agriculture [7,8].
Drought or water deficit directly impedes plant growth and productivity by causing loss of cell turgor and impairing mitosis that hinders cell elongation and division [9,10]. Osmotic stress is the primary signal in response to drought stress that induces abscisic acid (ABA) accumulation, which in turn, elicits several responses in plant cells [11,12]. As a secondary response, excessive formation of reactive oxygen species (ROS) such as hydroxyl radicals (OH−), hydrogen peroxide (H2O2), and superoxide radicals (O2•−) occurs due to drought in plant organelles like chloroplasts, mitochondria, and peroxisome [13,14]. These ROS disrupt the normal balance that exists between ROS production and scavenging [15]. This off-balance (due to excessive formation of ROS) not only inhibits the activity of various enzymes but also induces oxidative damage to cellular components such as DNA, protein, and lipids [15,16]. Concurrently, ROS affect cellular function and modulate stress-related primary and secondary metabolites and disturb redox homeostasis [9]. Moreover, ROS cause chlorophyll degradation and reduction of membrane stability [4,14]. A prolonged water deficit may cause cell death as a result of the massive production of ROS, which inhibits the scavenging action of the antioxidants machinery [17]. To prevent oxidative damage, plants have evolved adaptive mechanisms including upregulation of antioxidant defense system activity, which includes ROS-scavenger enzymes (e.g., ascorbate peroxidase (APX), catalase (CAT), glutathione reductase (GR), and superoxide dismutase (SOD)) and non-enzymatic antioxidants (e.g., glutathione, α-tocopherol, ascorbic acid, and phenolic compounds) [18,19,20]. Moreover, the accumulation of osmoprotectants (e.g., glycine betaine, soluble sugars, and proline) contributes to the maintenance of cell turgor by means of osmotic adjustment [4,21]. Therefore, under drought stress, it is imperative to provide sustainable strategies to support plants to resist such stress.
Gibberellins (GAs) are phytohormones involved in plant growth and development; stem and root elongation, leaf expansion, flowering, and seed germination, as GAs regulate various metabolic processes, activity of various enzymes, and gene expression [22,23]. Based on previous observations, gibberellic acid (GA3) plays a pivotal role in relieving abiotic stress [24,25,26]. Exogenous application of GA3 improves stomatal conductance, net photosynthesis rate, ion uptake, and hormonal balance [25]. Besides enhancing water use efficiency (WUE) [22,24], GA3 boosts antioxidant capacity [15], minimizes lipid peroxidation, and upregulates enzymatic antioxidants and osmoprotectants [27,28] to mitigate the adverse influences of drought stress. GAs crosstalk with other phytohormones to regulate several metabolic processes during plant growth [29,30]. The biosynthesis of GAs is promoted by indole-3-acetic acid, while GAs catabolize ABA [25,29].
Biostimulants are a promising sustainable strategy to stimulate plant growth and productivity and to strengthen the plant’s ability to mitigate abiotic stresses [19,31,32]. Although the use of commercially available plant growth stimulants such as osmoprotectants and/or antioxidants reduces the deleterious effects of abiotic stress, they are costly to growers. However, natural-based biostimulants such as plant-derived protein hydrolysate, Moringa oleifera leaves, propolis, maize grains, licorice roots, and diluted bee honey extracts are inexpensive by-products of plants or organisms that contribute to sustainable agriculture as an alternative to synthetic protectants [26,33,34,35,36,37,38,39]. The direct effect beyond the natural-based biostimulants is due to the fact that they contain many plant growth-promoting molecules such as antioxidants, osmoprotectants, mineral nutrients, and phytohormones. These growth-promoting molecules trigger physiological and biochemical changes, increase water and nutrient uptake, as well as promote resilience against abiotic stress including drought stress [31,36]. Diluted bee honey (Db-H) is a natural solution that mainly contains monosaccharides, disaccharides, and oligosaccharides [40,41]. Moreover, it contains various substances such as minerals, enzymes, proteins, lipids, organic acids, inorganic acids, and phenolic compounds (phenolic acids, flavonoids) [41,42]. Db-H serves as an active antioxidant in scavenging ROS [38,41] due to the presence of flavonoids that inhibit auto-oxidation [42] and enzymes that contribute to the removal of oxygen radicals [41], which are effective protection against drought-induced oxidative damage. As stated by Teklić et al. [32], Bulgari et al. [43], and Semida et al. [38], diluted honey extract as a plant biostimulator can increase tolerance to abiotic stress in plants. A recent field study highlighted the ability of Db-H-based plant biostimulants to alleviate salt stress in onions [38]. Indeed, Db-H applied to onion leaves showed higher biomass production, bulb yield, WUE, and leaf photosynthetic pigment contents. Moreover, Db-H promoted both enzymatic and non-enzymatic antioxidants, membrane integrity, and water content in onion tissues under the influence of salt stress.
However, to our knowledge, exogenous applications with Db-H as a natural biostimulant along with GA3 to plants grown under drought stress have not been studied before. Therefore, the current study was planned to evaluate the possibility of using some growth regulators; Db-H or GA3 as a promising tool to relieve the adverse influences of water deficit stress on Vicia faba productivity. This research is designed to examine potential positive changes in physio-biochemical attributes, antioxidant defense system activity, and accumulation of osmoprotectants in faba bean plants growing under the influence of drought stress and foliar application of Db-H or GA3. In this research, the potential improvement in plant growth, yield, WUE, and photosynthetic efficiency mediated by exogenous application of Db-H or GA3 under drought stress conditions was also evaluated.

2. Results

2.1. Growth and Green Pod Yield

The results in Table 1 show that drought stress significantly decreased the growth traits of Vicia faba plants (leaf area plant−1, the number of leaves plant−1, and shoot dry weight plant−1) by 22% and 23%, 26%, and 25%, and 41% and 43% in the 2018/2019 and 2019/2020 seasons, respectively, compared to the control. However, exogenously-applied GA3 or Db-H notably increased all growth traits (Db-H recorded better enhancements) compared to the corresponding control. Foliar application of GA3 or Db-H to drought-stressed plants resulted in positive effects on faba bean growth characteristics and recorded identical values for plants grown under full irrigation without the use of any growth regulator (100% of ETc). These effects of water deficit and foliar application of growth regulators on growth traits are reflected on the yield component. Irrigation of faba bean plants with 60% of ETc markedly decreased the green pods’ number plant−1 by 30% and 29% and green pods’ yield by 48% and 45% in both seasons, respectively, compared to the control (100% of ETc). However, exogenously-applied GA3 or Db-H to faba bean plants compensated the yield reduction occurred through inducing substantial increases in the number of green pods per plant by 65% and 66% and green pods yield by 134 and 138% (seasons average) in the plants subjected to 60% of ETc, respectively, when compared with the corresponding control. It can be seen that the corrective action of GA3 and Db-H can bring the pods yield achieved under drought stress to the same yield as achieved under optimum irrigation (100% of ETc). Under the tested irrigation regimes, WUE was differed, meaning that full irrigation recorded a WUE increase of 14% and 8% in both seasons, respectively, compared to the treatment of water deficit. The highest WUE corresponded with 100% of ETc × Db-H treatment, while the 60% of ETc × control treatment recorded the lowest WUE. However, foliar-applied GA3 and Db-H to drought-stressed faba bean plants increased WUE by 63% and 66% (seasons average), respectively, compared to those obtained under fully irrigated plants that were not treated with any of the growth regulators (Table 1).

2.2. Efficiency of the Photosynthetic Machinery

As displayed in Table 2, water deficit (660% of ETc) caused a considerable decrease in the leaf photosynthetic pigments (total chlorophylls and carotenoids contents), photochemical activity, SPAD chlorophyll index (soil–plant analysis development) values, and photosynthetic efficiency (Fv/Fm and performance index; PI) compared to full irrigation (100% of ETc).
Compared to untreated control plants, sprayed plants with GA3 or Db-H showed higher photosynthetic pigment contents, SPAD chlorophyll index, photochemical activity, and the efficiency of PSII. In fully irrigated plants, application of GA3 or Db-H increased total chlorophylls by 15% and 24%, total carotenoids by 10% and 18%, photochemical activity by 8% and 13%, SPAD index by 8% and 14%, Fv/Fm by 6% and 11%, and performance index by 7% and 20% (seasons average), respectively, in comparison to the corresponding control. Foliage-applied GA3 or Db-H alleviated the negative effects on the photosynthetic machinery in drought-stressed faba bean plants. In deficit-irrigated plants, the increases in the photosynthetic machinery (total chlorophylls, total carotenoids, photochemical activity, SPAD chlorophyll index, Fv/Fm, PI) were 59% and 62%, 27% and 31%, 32% and 32%, 40% and 41%, 18% and 21%, and 52% and 53% (seasons average), respectively, compared with the corresponding control.

2.3. Leaf Tissue Stability and Oxidative Stress Indicators

Faba bean leaf tissue stability was assayed as the membrane stability index (MSI), electrolyte leakage (EL), and relative water content (RWC) (Table 3). For irrigation levels, the adverse effects of drought-induced stress on Vicia faba plants were described as decreases in RWC and MSI by 16% and 20%, while EL increased by 75% (seasons average), respectively, compared to irrigation with 100% of ETc. Regarding the foliar application of growth regulators, application of GA3 or Db-H elevated both RWC and MSI, while minimized EL compared to untreated plants (control). However, GA3 or Db-H supplementation markedly attenuated the drought-induced damage to tissue stability in faba bean plants, as the same RWC, MSI, and EL values were recorded for well-watered plants that were not treated with any of the growth regulators.
The utility of the oxidative damage indicators identified in this study was lipid peroxidation, expressed in malondialdehyde (MDA) content, hydrogen peroxide (H2O2), and superoxide (O2•−) contents (Table 3). For irrigation level, when irrigation level decreased from 100% to 60% of ETc, MDA, H2O2, and O2•− contents increased by 67%, 58%, and 102%, and 67%, 60%, and 100% in both seasons, respectively. Regarding the growth regulator applications, GA3 or Db-H significantly decreased levels of MDA, H2O2, and O2•− compared to the control. For integrative treatments under full irrigation, the best treatments were 100% of ETc × GA3 or Db-H which significantly decreased the oxidative stress biomarkers. Under water deficit (60% of ETc), the best treatment was 60% of ETc × GA3 or Db-H, which significantly reduced MDA, H2O2, and O2•− contents by 64% and 69%, 52% and 54%, and 69% and 69% (seasons average), respectively, compared to the corresponding control (60% of ETc).

2.4. Osmoprotectant Compounds

Results of Table 4 display the contents of the osmoprotectants in terms of soluble sugars, free proline, glycine betaine, and total soluble protein, which increased significantly by 43%, 64%, 85%, and 21% (seasons average) in drought-stressed plants. Nevertheless, under different irrigation regimes, the application of GA3 or Db-H increased the contents of soluble sugars, free proline, and glycine betaine contents, while the total soluble protein content was decreased. Under optimum irrigation (100% of ETc), the increases were 43% and 74%, 31% and 31%, and 38% and 38% (seasons average), respectively, compared with the respective control. For osmotically-stressed plants sprayed with GA3 or Db-H, the elevations in the soluble sugars, free proline, and glycine betaine contents were 13% and 27%, 21% and 23%, and 30% and 32% (seasons average), respectively in comparison to the corresponding control.

2.5. Antioxidant Defense System Components

The contents of non-enzymatic antioxidants (glutathione (GSH), ascorbic acid (AsA), and α-tocopherol (α.TOC)) (Table 5), and enzymatic antioxidant activities (superoxide dismutase (SOD), glutathione reductase (GR), catalase (CAT), and ascorbate peroxidase (APX)) (Table 6) were increased by 49%, 74%, 40%, 25%, 55%, 51%, 60%, and 69% (seasons average), respectively, under the irrigation level of 60% of ETc compared to well-watered plants. However, foliar-applied GA3 or Db-H substantially elevated the antioxidant capacity, while the total phenolic compounds were decreased. Under full irrigation, exogenously-applied GA3 or Db-H increased the activities of AsA (by 27% and 53%), GSH (by 29% and 58%), α.TOC (by 20% and 37%), SOD (by 16% and 15%), CAT (by 28% and 27%), GR (by 26% and 25%), and APX (by 14% and 14%) (seasons average), respectively, compared with the respective control, but not reached the activities obtained under drought stress.
Under water deficit stress, treatment with GA3 or Db-H increased these antioxidant activities by 16% and 16%, 21% and 24%, 11% and 12%, 25% and 26%, 15% and 15%, 21% and 20%, and 18% and 18% (seasons average), respectively, in relation to the corresponding control, and markedly exceeded those obtained under full irrigation (100% of ETc) treatment.

2.6. Nutrient Contents

In both seasons, faba bean plants exposed to a water deficit showed significant reductions in the contents of N (by 21%), P (by 23%), K (by 19%), Fe (by 20%), Mn (by 20%) and Zn (by 20%) in comparison to fully irrigated plants (Table 7). Regardless of irrigation levels, applying growth regulators (GA3 or Db-H), especially Db-H, markedly increased the nutrient contents compared to untreated plants. Foliar-applied GA3 or Db-H attenuated the adverse impact of drought on plant nutritional status. Where, 60% of ETc × GA3 or Db-H treatment exhibited higher nutrient contents compared with 60% of ETc, recording values similar to or higher than values of full irrigated plants. The greatest nutrient contents were obtained under 100% ETc × Db-H treatment.

2.7. Phytohormone Concentrations

The phytohormone analyses (IAA, GA3, CKs, and ABA) displayed differences between the two irrigation regimes (Table 8). Drought-stressed plants exhibited lower IAA (by 23%), GA3 (by 26%), and CKs (by 25%), and higher ABA (by 50%) (seasons average) than non-stressed plants. As for the application of plant growth regulators, GA3- or (Db-H)-treated Vicia faba plants showed higher IAA, GA3, and CKs contents, and lower ABA content than untreated plants.
The combination of these two factors (irrigation regimes and growth regulators) significantly increased IAA, GA3, and CKS contents, while decreased ABA content (Table 8). Interactive application of GA3 or Db-H + full irrigation (100% of ETc) increased IAA (by 20% and 55%), GA3 (by 118%% and 39%), and CKs (by 36% and 68%) (seasons average) compared to the respective control. Similarly, foliar-applied GA3 or Db-H to plants subjected to water deficit (60% of ETc) notably increased IAA (by 45% and 74%), GA3 (by 172% and 59%), and CKs (by 48% and 98%), while decreased ABA (by 49% and 59%) (seasons average) compared to the corresponding control.

3. Discussion

In dry regions including Egypt, drought stress is the major constraint to most crop plants, seriously limiting plant growth and productivity and regulating metabolism through complex and various mechanisms linked to plant metabolic pathways [4,12]. Under constant water deficit, plants are unable to withstand such stress through the available endogenous antioxidant defense system as in the case of the Vicia faba plants used in the current research. Therefore, Vicia faba plants must be supported by exogenous plant growth regulators that may stimulate several physio-biochemical processes, increase plant performance, and enhance resilience against water deficit stress. As presented in Table 10, Db-H analysis showed that this promising tool for sustainable cultivation is a plant growth biostimulator for drought-stressed bean plants. Db-H is rich in osmoprotectants (i.e., proline, total amino acids, and soluble sugars), different sugars, and mineral nutrients (i.e., K, P, Mg, Ca, S, Fe, Mn, Zn, Cu, I, Na, and Se). Additionally, it has high values of vitamins (vitamin C and B-group vitamins). Moreover, Db-H possesses a high value of DPPH radical-scavenging activity (88.2%), which is widely used for screening the antioxidant activity to prevent lipid peroxidation [17,38], which confers the antioxidant property of Db-H. Moreover, exogenously-applied GA3 has been reported to induce various metabolic reactions to ameliorate abiotic stress [27,44]. Therefore, as shown in the current study, both GA3 and Db-H have crucial mechanisms in favor of drought-stressed Vicia faba plants to boost their tolerance to drought stress.
In this study, lowering the irrigation level from 100% to 60% ETc restricted faba bean performance (growth and productivity; Table 1), impaired efficiency of photosynthesis machinery (Table 2), and disrupted leaf tissue stability (RWC and MSI; Table 3). As a result, lipid oxidation (MDA) was increased as a result of the excessive generation of oxidative stress markers (H2O2 and O2•‒) (Table 3), associated with increased osmoprotectant compounds (Table 4), and upregulation of non-enzymatic (Table 5) and enzymatic antioxidants (Table 6), which cope with oxidative damage under drought stress [20]. Adverse effects exacerbated by water deficit may be ascribed to osmotic stress with loss of cell turgor and/or ROS overproduction under drought stress [11,23,45]. Nonetheless, foliar-applied GA3 or Db-H ameliorated the adverse impacts caused by drought stress on the growth of faba bean plants, thus enhancing green pods yields to be comparable to those of well-watered plants that had not been treated with growth regulators, thus increasing WUE. Under irrigation with 100% of ETc, the improvement in growth and yield of bean plants was more evident by Db-H foliar spray resulting in higher WUE. The recovery of growth and productivity of drought-stressed Vicia faba plants by application of GA3 or Db-H revealed that these growth regulators may include mechanisms to mitigate the effects of drought-induced stress. This is likely attributed to the growth-related metabolites of Db-H dissolved substances such as proline, soluble sugars, amino acids, antioxidants, vitamins, and mineral nutrients, which support plants to restore their growth and development under drought stress [46,47]. Furthermore, GA3 upregulates the expression of genes (xyloglucan endotransglycosylases, expansins, and cyclin-dependent protein kinases) involved in increased cell division and elongation [48]. Moreover, GA3 induces osmoregulation by maintaining the osmotic potential, promoting enzyme activity, improving membrane permeability to facilitate mineral nutrient uptake and photosynthesis transportation [22,49,50], thus stimulating plant growth and biomass production (Table 1).
RWC is a physiological indicator of available water content in favor of tissue metabolism, while the degree of membrane integrity can be assessed as MSI and EL [51,52]. Both growth regulators (Db-H and GA3) mediated recovery of stressed leaf tissues by increasing cell turgor (RWC) and membrane integrity (MSI), while ion leakage (EL) was reduced (Table 3). The improvement in RWC of drought-stressed plant tissues and cells helped maintain cell turgor through the accumulation of osmolytes such as proline, soluble sugars, and glycine betaine (Table 4) due to Db-H and GA3 application and/or changes in elasticity of the cell wall [9,53]. This allowed for continued metabolic activities as effective mechanisms for drought tolerance in stressed faba bean plants. RWC enhanced by exogenous application of Db-H or GA3 was closely related to increased WUE in faba bean plants. (Table 1). In this study, the increased protective compounds such as osmoprotectants, enzymatic antioxidants, and low molecular-weight antioxidants (Table 4, Table 5 and Table 6) by foliar-supplemented Db-H or GA3 protected plasma membranes from lipid peroxidation (in term of MDA) by decreasing H2O2 and O2•‒ contents (Table 3). These findings may be related to improved MSI, decreased EL and photo-oxidation, and enhanced membrane integrity against oxidative damage [38,46], and thus improved faba bean plant growth and outputs under water deficit stress.
In the current study, leaf photosynthetic pigment contents (total chlorophylls and carotenoids), photochemical activity, SPAD chlorophyll index, and photosynthetic efficiency (Fv/Fm and PI) were reduced while the irrigation water was reduced to 60% ETc, indicating chlorophyll degradation in chloroplasts and photoinhibition of PSII of water-stressed faba bean plants due to the damaging influences of ROS [54,55]. However, leaf photosynthetic pigment contents, photochemical activity, SPAD chlorophyll index, and photosynthetic efficiency (Table 2) were markedly improved by foliar-applied Db-H [38] or GA3 [22]. These results may be related to maintaining cell membrane integrity and increasing leaf RWC by Db-H or GA3 supplementation. Both Db-H and GA3 likely mitigated the negative effects of drought, and faba bean plants responded to drought stress by up-regulation of osmoprotectants (Table 4), non-enzymatic (Table 5) and enzymatic antioxidants (Table 6) for ROS-scavenging to minimize lipid peroxidation. In line with our findings, GA3 supplementation improved leaf chlorophyll content in wheat [27] and maintained the photosynthetic efficiency of PSII in laurel seedlings [56]. Additionally, Db-H is rich in nutrients to maintain intercellular hemostasis of ions required for photosynthetic biosynthesis, thus improving the efficiency of the photosynthetic machinery of Vicia faba plants.
Nutrients deficiency in plants that is attributed to the osmotic impact of water deficit stress and/or soil water deficit disturbs nutrient availability, uptake, translocation, and metabolism [9], which lead to the reduction of macro-and micro-nutrients contents in drought-stressed faba bean (Table 7). Nevertheless, foliar-applied GA3 or Db-H induced ion hemostasis and increased mineral nutrient contents of drought-stressed plants. This may be attributed to that exogenous application of GA3 or Db-H increased root uptake surfaces resulting from increased root system volume (data not shown), and/or increased accumulation of osmoprotectants (Table 4) to balance the osmotic pressure in organelles, thus mainlining cell turgor and improving nutritional status and water uptake [57].
In this work, the plant defense machinery including synthesis of osmoprotectants (proline, soluble sugars, glycine betaine, and total soluble protein; Table 4), and both non-enzymatic antioxidants contents (AsA, GSH, and α.TOC; Table 7), and enzymatic antioxidants activities (SOD, CAT, GR, and APX; Table 6) increased in growth regulators (GA3 and Db-H)-treated plants. This positive situation protected faba bean plants from the deleterious impacts of water deficit stress by osmotic adjustment and ROS-scavenging [15,38]. Increased osmoprotectants are likely to lead to the uptake or breakdown of Db-H as biostimulants, given that it is rich in osmoprotectant compounds (Table 9). Furthermore, GA3 regulates different genes that can modulate the osmotic ability to maintain cell enlargement through the accumulation of osmotically active solutes such as soluble sugar, soluble protein, free proline, and glycine betaine [28,58]. Our results showed that drought stress in combination with either of the growth regulators (GA3 or Db-H) markedly improved the antioxidant defense system to enable Vicia faba plants to withstand drought stress through protection from oxidative damage as evidenced by the decreased contents of MDA, H2O2, and O2•‒ (Table 3).
It has been well demonstrated that phytohormones play an important role in various physiological, biochemical, and molecular processes in plants to mitigate drought stress [59], which was significantly increased by exogenous application of GA3 or Db-H, while ABA content was reduced (Table 8). In this study, Db-H promoted the contents of IAA, CKs, and GA3 in faba bean plants subjected to drought stress (Table 8), which could be attributed to the increased mineral nutrients required for the formation of protoplasm and phytohormones [38]. According to Semida and Rady [34], presoaking bean seeds with some extracts resulted in higher contents of IAA and GA3, while decreased ABA. Different genes are expressed after GAs treatment highlighting that GAs upregulated genes related to IAA and other genes related to ABA are down-regulated by GAs [58], while CKs have antagonistic roles against ABA [34]. Further, GAs-induced degradation of DELLA proteins is modulated by different signals such as salinity and drought, and other hormones [60], revealing that GAs regulate and crosstalk with other phytohormones to ameliorate the deleterious effects of drought stress. Water deficit stress disrupts the hormonal balance in plants, and thus, hormonal hemostasis may be a means for GA3-induced drought stress tolerance [25].
Finally, the negative effects of environmental foes may exceed the natural endurance of stressed plants. In this case, the components of a stressed plant’s defense system do not meet adequate defense requirements, and therefore external use of auxiliary substances such as nutrients and other beneficial strategies increases the efficiency of antioxidant defenses, and thus plants can perform efficiently under adverse conditions of environmental foes [61,62,63,64,65].

4. Materials and Methods

4.1. Experimental Location and Soil Properties

Using a private farm (Fayoum; 29.3452 N, 30.5686 E, Egypt), two experiments were conducted at the field level during two consecutive winter seasons (2019 and 2020). The soil, 0.90–1.0 m deep, with loamy sand texture, which is classified as Typic Torripsamments, siliceous, hypothermic [66]. The soil physical and chemical properties were performed applying methods described in Klute [67] and Page et al. [68], and results are shown in Table 10. The electrical conductivity of the tested soil was 8.23 dS m−1, being saline soil according to the classification of Dahnke and Whitney [69].

4.2. Planting, Treatments, and Experimental Layout

The seeds of Vicia faba (cv. Giza 40; widespread cultivar of faba bean in the study area based on the recommendation of the Egyptian Ministry of Agriculture) were secured from the Agricultural Research Center, Egypt. Firstly, the seeds were washed with distilled water then sterilized with sodium hypochlorite solution (1%; v/v) for roughly two min, once more the seed surface was cleaned from sterilization solution with distilled water after that were kept at room temperature to dry. The seeds were sown on October 20, for both seasons (2019 and 2020) in hills with plant and row spacing of 25×70 cm. Each plot area was 10.5 m2; 3.5 m length (5 rows) × 3 m width.
In this study, there are two treatment factors; including irrigation regimes and exogenous application of plant growth regulators. Two irrigation regimes were applied corresponding with 100% and 60% of the crop evapotranspiration (ETc). Gibberellic acid (GA3) and diluted bee honey (Db-H) were applied at 20 mg and 20 g L−1, respectively, as foliar spraying. These concentrations were selected based on our preliminary pot study (Table S1). The irrigation treatments were separated by a 1 m non-irrigated area. Until the full emergence of seedlings (15 days after planting; DAP), the faba bean plants were irrigated at 100% of ETc to ensure good plant establishment, thereafter the two irrigation treatments were initiated. These two irrigation treatments were chosen based on our preliminary pot study (Table S1). Fifteen days after the initiation of the irrigation treatments, GA3 and Db-H were applied as foliar spraying in the early morning. Fifteen days after the first spraying, the second foliar spray was implemented for faba bean plants. Sprays were conducted to run-off, with the use of Tween-20 (0.1%, v/v) as a surfactant to ensure optimum penetration into leaf tissues. The plants (n = 200) in each experimental unit (10.5 m2) were sprayed with 2 L of spray solution, which was increased to 2.4 L for the second time of spraying. The experimental layout for each treatment was designed as a Randomized Split Plot with three replications. Different fertilizers (5 tons organic manure, 50 kg potassium humate, 75 kg of P2O5 using Ca(H2PO4)2; 15.5% P2O5, 60 kg of K2O using K2SO4; 48% K2O, and 45 kg of N using (NH4)2SO4; 21% N were added per hectare) and agronomic practices were applied following the recommendations of the Agricultural Research Center, Giza, Egypt.

4.3. Irrigation Water Applied (IWA)

The reference evapotranspiration (ETo) was given using the class A pan data (Epan; mm day−1), adjacent to the experimental plots adjusted with appropriate pan coefficient (Kpan) and the crop coefficient (Kc) [70]. The ETc (mm day−1) was determined as the following formula [70]:
ETc = Epan × Kpan × Kc
Irrigation water applied (IWA) was computed with an equation as follows:
IWA = (A × ETc × Ii × Kr) / [Ea × 1000 × (1 − LR)]
where, IWA = irrigation water applied (m3), A = area of plots (m2), ETc = crop water requirements (mm per day), Ii = intervals of irrigation (day), Kr = covering factor, Ea = efficiency of application (%), and LR = requirements for leaching.
The total irrigation water applied during both winter seasons was 3690 and 2214 m3 ha−1 in the 2019 season and 3754 and 2252 m3 ha−1 in the 2020 season for 100 and 60% of ETc, respectively. The digital moisture meter sensors (HH2 type, Cambridge, CB5 0 EJ, UK) were utilized to record the water content of the tested soil every two days at different depths, 0–15 and 15–30 cm.

4.4. Bee Honey Analysis for Physico-Chemical Composition

Clover honey used in the current study was analysed for effective components and results are shown in Table 10. Moisture (%), proline, and pH were assessed according to AOAC [71]. Quantities of sugars by High-Performance Liquid Chromatography (HPLC) were measured as the concentration of fructose, glucose, maltose and sucrose (%) according to Bogdanov and Baumann [72]. Mineral nutrients were measured according to the methodology given in [73]. Ascorbic acid concentration was determined according to Mukherjee and Choudhuri [74]. Determination of the antioxidant activity was performed using 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay as described by Lee et al. [75].

4.5. Sampling and Measurements

4.5.1. Growth and Yield Characteristics, and WUE

Plant growth characteristics were analyzed at sixty DAP in each season, 5 plants were selected, randomly, from each plot (main and sub-main plots). The number of branches and leaves for each plant was counted. The leaf area (cm2) was measured using a held-hand planimeter (Planix 7, Tamaya Technics Inc. Tokyo, Japan). The shoot was weighed for each plant to determine to shoot fresh weight (g). For recording shoot dry weight (g), shoots were oven-dried at 70 ± 2 °C until a constant weight was reached.
On the same date (60 DAP), green pods yield parameters were recorded in terms of the number of green pods per plant and green pods’ weight (ton) per hectare. These parameters of green pods yield were measured using the two outer rows of each experimental plot. The WUE was calculated as presented by Jensen [76]:
WUE = [Green pods yield (kg m−2)]/[irrigation water applied (m−3 m−2)]

4.5.2. Efficiency of the Photosynthetic Machinery

Leaf photosynthetic pigment contents were determined in terms of chlorophylls and carotenoids based on the Arnon [77] procedures. Homogenization in 80% acetone (v/v) and centrifugation at 10,000× g for 10 min were implemented. The acetone extract solution absorption was recorded at 663, 645, and 470 nm in a UV–Visible spectrophotometer (UV-160A, Shimadzu, Japan).
Photochemical activity in fresh ear leaf was determined using the Ferricyanide technique as depicted by Jagendorf [78] with some modifications given in the Avron [79] method.
Using the SPAD-502 chlorophyll meter (Minolta, Osaka, Japan), the relative chlorophyll content (soil–plant analysis development (SPAD index) values) was measured. The measurements of chlorophyll “a” fluorescence were performed using a handy PEA chlorophyll fluorometer (Hansatech Instruments Ltd., Kings Lynn, UK). The maximum quantum yield of PSII (Fv/Fm) was determined using the equation: Fv/Fm = (Fm ‒ F0)/Fm [80]. The photosynthesis performance index (PI) that quantifies multi-parameters as electron flow rate, absorption, trapping, and dissipation of excitation energy, was computed as described by Clark et al. [81].

4.5.3. Leaf Tissue Stability and Oxidative Stress Biomarkers

Using the fully enlarged upper leaves, the Osman and Rady [82] procedure was practiced to assess the leaf relative water content (RWC). Midribs were excluded and the leaf blades were divided into 2 cm-diameter discs, which were immediately weighed (fresh mass). The discs were then saturated by deionized water for 24 h in the dark, gently surface-dried from the adhering water drops to record the turgid mass. To record dry mass, discs drying was implemented for 48 h under 70 °C, and the following equation was utilized for calculating RWC percentage:
RWC (%) = [(fresh mass − dry mass)/(turgid mass − dry mass)] × 100
Using the fully enlarged upper leaves, midribs were excluded and the leaf blades were divided into 0.2 g leaf pieces to evaluate leaf membrane stability index (MSI) [83]. A sample (0.2 g) was immersed in 10 ml of ion-free water and 40 °C for 30 min was practiced to record EC1. Another 0.2 g sample was boiled for 10 min to record EC2. The following equation was utilized for calculating MSI percentage:
MSI (%) = [1 − (EC1/EC2)] × 100
Using fully enlarged upper leaves, midribs were excluded and the leaf blades were divided into discs to assess ions leaked from leaf tissue [83]. Using 20 discs immersed in 10 ml of ion-free water, EC0 was recorded. EC1 was then measured after heating the tube content at 45–55 °C for 30 min. Then, the content of the tube was boiled for 10 min to record EC2. The following equation was utilized for calculating electrolyte leakage (EL) percentage:
EL (%) = [(EC2 − EC1)/EC3] × 100
Determination of lipid peroxidation that assessed as malondialdehyde (MDA), and the two biomarkers of oxidative stress; superoxide (O2•‒), and hydrogen peroxide (H2O2) contents were implemented applying the procedures of Madhava Rao and Sresty [84], Velikova et al. [85], and Kubiś [86], respectively. The contents of MDA were assessed applying an extinction coefficient (155 mM−1 cm−1) and presented as µmol g−1 FW. The H2O2 content (µmol g−1 FW) was evaluated colorimetrically at 390 nm and the calculations were performed based on a proper standard curve. The O2•− content (µmol g−1 FW) was evaluated using sample fragments (1 × 1 mm, 0.1 g) that flooded using a buffer (K-phosphate, 10 mM, pH 7.8), which was mixed with each of NBT (0.05%) and NaN3 (10 mM) for 60 min under 25 °C. The mixture was subjected to 85 °C for 15 min. The mixture was then cooled rapidly. The absorbance readings were taken at 580 nm.

4.5.4. Contents of Osmoprotectant Compounds

Using toluene, extraction of proline was practiced and at 520 nm, the absorbance was recorded [87]. Leaf content (μg proline g−1 FW) of proline was calculated using a suitable standard curve. Glycine betaine (GB) content was estimated under acidic conditions through monitoring formed periodide crystals colorimetrically (at 365 nm) after reaction of the mixture with a reagent (cold KI‒I2) [88]. By utilizing a professional method [89], extraction (with 96% ethyl alcohol), and determination of the content of total soluble sugars (mg g−1 DW). The reaction of the ethanolic extract (100 µL) was implemented with 150 mg of anthrone as a reagent prepared, freshly, in 100 mL H2SO4, 72%. Then, the mixture was boiled for 10 min and readings were taken at 625 nm after cooling. The procedures described in Bradford [90] were used to determine total soluble protein content.

4.5.5. Contents of Non-Enzymatic Antioxidant Compounds

Ascorbate (AsA) was determined in the tissue of the upper fully-expanded leaf after the homogenization in HPO3 (ice-cold, 5%) contained 1 mM EDTA. The produced homogenates were centrifuged at 4,000 × g for 20 min, and supernatants were used to estimate AsA [91]. Determination of glutathione (GSH) was performed [92] with a minor modification [93] and a known concentration of GSH was used as a standard curve. α-Tocopherol (α-TOC) was detected according to the method of Ching and Mohamed [94] and Konings et al. [95]. The total leaf content of phenolic compounds was assessed by the Folin–Ciocalteu method [96] functioning gallic acid as a standard. At 725 nm, the absorbance readings were recorded and the total phenolic contents were presented as mg gallic acid equivalents (GAE) g−1 dry weight, computed from a standard curve prepared with gallic acid.

4.5.6. Activities of Antioxidant Enzymes

The fully enlarged upper leaves were used to extract enzymes in 0.5 g. An ice-cold buffer, pH 7.0 (e.g., 100 mM K-phosphate, which contained 1% PVP) was utilized with a pre-chilled (cleaned) mortar and pestle to macerate leaf samples. The obtained homogenates were transferred for the centrifugation process at 12,000× g for 0.25 h under 4 °C. The obtained supernatants were the enzymatic extracts, which were utilized for assaying the activities of catalase (CAT), glutathione reductase (GR), and ascorbate peroxidase (APX). Using the method detailed in Aebi [97], assaying of the CAT activity (Unit mg−1 protein) was performed using a spectrophotometer apparatus at 240 nm. To assay the ability of the enzyme to decompose the H2O2 for 2 min, 2 mL of the reaction mixture of a P-buffer (50 mM, pH 6.0), EDTA (0.1 mM), H2O2 (0.02 M), and 0.1 mL of the enzymatic extract was applied, and an extinction coefficient (39.4 mM−1 cm−1) was also applied. The Nakano and Asada [98] method was applied to assay the APX activity (Unit mg−1 protein). Using spectrophotometer, 2 mL mixture (P-buffer (50 mM, pH 7.5), EDTA (100 µM), AsA (300 µM), 0.1 mL H2O2, and 0.1 mL enzyme extract) was observed for 2 min at 290 nm, and 2.8 mM−1 cm−1 was applied as an extinction coefficient. The Foster and Hess [99] method was applied to assess the GR activity (Unit mg−1 protein) by monitoring (for 3 min at 340 nm) the changes that occurred in the reading of the reaction mixture (K-phosphate buffer (0.1 M, pH 7.0), EDTA (100 µM), NADPH (0.5 mM), GSSG (0.1 mM), and 0.1 mL enzyme extract).
Homogenization with ice was performed for frozen samples (500 mg) and the homogenization solution was 10 mL of 50 mM L−1 HEPES buffer and 0.l mM L−1 Na2EDTA (pH 7.6). To obtain a crude extract, centrifugation was practiced for homogenates for a quarter of an hour at 15,000× g under 4 °C, which was functioned for assaying protein and superoxide dismutase (SOD). Overnight, dialyzing of crude extract was performed against a diluted homogenizing solution to eradicate the interference in SOD assay from substances having low molecular weights. The protein-dye binding method [90] was functioned to assess the concentration of soluble protein against a standard (bovine serum albumin). Assaying the SOD (EC 1.15.1.1) activity was implemented through inhibiting NBT photochemical reduction under practicing the Yu and Rengel [100] method.

4.5.7. Contents of Nutrient Elements

Digestion process was performed for the dried leaf samples with a mixture consisting of perchloric and nitric acids (at 1: 3, v/v, respectively). Using the previous digestion solution, assessments of N, P, and K+ contents were performed. Determination of N was performed using the micro-Kjeldahl apparatus (Ningbo Medical Instruments Co., Ningbo, China) following [101]. The P content was assessed following the blue color method [102] whereby molybdenum was used to reduce molybdophosphoric in sulfuric acid while reducing to exclude arsenic. The K+ content was assessed utilizing a flame photometer (Perkin-Elmer Model 52-A, Glenbrook, Stamford, CT, USA) device as depicted in the methods of Page et al. [68]. Micronutrients (Zn, Mn, and Fe) contents were detected in dried leaf samples according to Johnson and Ulrich [103] with atomic absorption spectroscopy under checking against standard reference samples (NIST, USA).

4.5.8. Contents of Plant Hormones

The phytohormones; indole-3-acetic acid (IAA), gibberellic acid (GA3), cytokinins (CKs) profiling were implemented based on the procedures of gas chromatography-mass spectrometry (GC-MS) methods improved by Nehela et al. [104] with minor adjustments [26]. Fresh leaves (0.1 g) sample was extracted in ice-cold extraction solvent (2 mL; methanol/water/HCl (6N); 80/19.9/0.1; v/v/v). Then, the extract was centrifuged at 25,000× g, 4 °C for 5 min. Supernatants were collected and concentrated to 50 μL under N stream and then stored at −80 °C until analysis. For IAA, 50 μL of the supernatant was derivatized with 40 μL of MCF then concentrated to 20 μL under N stream and 0.5 mg of Na2SO4 were added to dry the organic phase. For CKs and GA3, 50 μL from the supernatant was dried and derivatized with 100 μL of N-Methyl-N-(trimethylsilyl) trifluoroacetamide (MSTFA) by heating at 85 °C for 45 min. For GC–MS analysis, 1 μL was injected into the GC–MS running in the selective ion mode (SIM-mode). All samples and phytohormone standards were analysed using a Clarus 680 GC with SQ8-T Mass Spectrometer system (Perkin Elmer, Waltham, MA, USA) fitted with an Elite-5MS capillary column (low bleed, 30 m × 0.25 mm × 0.025 μm film thickness; Perkin Elmer, Waltham, MA, USA). Helium was the carrier gas with a flow rate of 1 mL min−1. The temperature program for IAA was as the following: the column was held at 50 °C for 3 min, and then increased to 200 °C at a rate of 4 °C min−1, held for 5 min. While, the program for CKs and GA3 was as the following: the column was held at 60 °C for 2 min and then increased to 160 °C at 20 °C min−1, and finally to 290 °C at 5 °C min−1. The injector and the detector temperatures were set at 250 °C and 260 °C, respectively. The TurboMass software version 6.1 (Perkin Elmer, Waltham, MA, USA) was used to analyze chromatograms. Identification of IAA, CKs and GA3 was performed by comparing their retention time, linear retention indices (LRIs) and the selected ions with those of authentic standards. Extraction and estimation of the content of abscisic acid (ABA) were implemented using high-performance liquid chromatography (HPLC) as outlined by Ünyayar et al. [105].

4.6. Statistical Tests

The data were analyzed based on the GLM procedures of the GENSTAT software (VSN International Ltd, Oxford, UK). All data were subjected to the combined analysis and the mean differences were compared with the least significant difference (LSD) test at 5% probability (p ≤ 0.05) level. The analyzed results are presented as the mean ± standard error.

5. Conclusions

The current study exhibits differences in physiological, biochemical, and metabolic responses among the (Db-H)- or GA3-treated and untreated faba bean plants. Exogenous application of Db-H or GA3 markedly elevated the level of non-enzymatic and enzymatic antioxidants and osmoprotectants (proline, glycine betaine, soluble sugars, and soluble protein) as well as increased the phytohormones (indole-3-acetic acid and gibberellic acid and cytokinins), this associated with the reduction of malondialdehyde (MDA) and abscisic acid (ABA). Foliar applied Db-H or GA3 improved the nutrients status, tissue health, leaf photosynthetic pigments, and photosynthetic efficiency leading to higher growth and productivity (yield and water use efficiency) of drought-stressed faba bean plants. Therefore, the application of these growth regulators (Db-H and GA3) was identified to be an effective strategy to mitigate the damage effects of irrigation water deficits for sustainable faba bean production in arid and semi-arid areas.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/plants10040748/s1, Table S1: A preliminary pot study conducted to identify the optimal concentration of diluted bee-honey (Db-H) and gibberellic acid (GA3), as well as identifying the drought threshold of faba bean (Giza 40 cultivar) for the main study.

Author Contributions

Conceptualization, M.M.R., S.H.K.B., T.A.A.E.-M. and M.A.S.E.-Y.; Data curation, M.M.R., S.H.K.B. and T.A.A.E.-M.; Formal analysis, M.M.R., S.H.K.B., T.A.A.E.-M., M.A.S.E.-Y. and A.A.; Investigation, M.M.R., S.H.K.B., T.A.A.E.-M., M.A.S.E.-Y., E.F.A., F.A.S.H. and A.A.; Methodology, M.M.R., S.H.K.B., T.A.A.E.-M. and A.A.; Resources, M.M.R., S.H.K.B., T.A.A.E.-M., M.A.S.E.-Y., E.F.A., F.A.S.H. and A.A.; Software, M.M.R., S.H.K.B., T.A.A.E.-M., M.A.S.E.-Y., E.F.A., F.A.S.H. and A.A.; Writing—original draft, M.M.R., S.H.K.B., T.A.A.E.-M., M.A.S.E.-Y., E.F.A., F.A.S.H. and A.A.; Writing—review and editing, M.M.R., E.F.A., F.A.S.H. and A.A. All authors have read and agreed to the published version of the manuscript.

Funding

The Deanship of Scientific Research at Taif University through the research number TURSP-2020/143 is acknowledged.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available upon request from the corresponding author.

Acknowledgments

The authors are thankful to the Taif University Researchers Supporting Project number (TURSP-2020/143), Taif University, Taif, Saudi Arabia for providing the financial support and research facilities.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples of faba bean plant are available from the authors.

References

  1. Semida, W.M.; Taha, R.S.; Abdelhamid, M.T.; Rady, M.M. Foliar-applied α-tocopherol enhances salt-tolerance in Vicia faba L. plants grown under saline conditions. S. Afr. J. Bot. 2014, 95, 24–31. [Google Scholar] [CrossRef] [Green Version]
  2. Karkanis, A.; Ntatsi, G.; Lepse, L.; Fernández, J.A.; Vågen, I.M.; Rewald, B.; Alsiņa, I.; Kronberga, A.; Balliu, A.; Olle, M.; et al. Faba bean cultivation—Revealing novel managing practices for more sustainable and competitive European cropping systems. Front. Plant Sci. 2018, 9, 1–14. [Google Scholar] [CrossRef]
  3. Khazaei, H.; Vandenberg, A. Seed Mineral Composition and Protein Content of Faba Beans (Vicia faba L.) with Contrasting Tannin Contents. Agronomy 2020, 10, 511. [Google Scholar] [CrossRef] [Green Version]
  4. Semida, W.M.; Abdelkhalik, A.; Rady, M.O.A.; Marey, R.A.; Abd El-Mageed, T.A. Exogenously applied proline enhances growth and productivity of drought stressed onion by improving photosynthetic efficiency, water use efficiency and up-regulating osmoprotectants. Sci. Hortic. 2020, 272, 109580. [Google Scholar] [CrossRef]
  5. Abdelkhalik, A.; Pascual, B.; Nájera, I.; Domene, M.A.; Baixauli, C.; Pascual-Seva, N. Effects of deficit irrigation on the yield and irrigation water use efficiency of drip-irrigated sweet pepper (Capsicum annuum L.) under Mediterranean conditions. Irrig. Sci. 2020, 38, 89–104. [Google Scholar] [CrossRef]
  6. AQUASTAT. AQUASTAT—FAO’s Global Information System on Water and Agriculture; Food and Agriculture Organization: Rome, Italy, 2019. [Google Scholar]
  7. Pal, S.; Zhao, J.; Khan, A.; Yadav, N.S.; Batushansky, A.; Barak, S.; Rewald, B.; Fait, A.; Lazarovitch, N.; Rachmilevitch, S. Paclobutrazol induces tolerance in tomato to deficit irrigation through diversified effects on plant morphology, physiology and metabolism. Sci. Rep. 2016, 6, 1–13. [Google Scholar] [CrossRef]
  8. Abdelkhalik, A.; Pascual-Seva, N.; Nájera, I.; Domene, M.Á.; Baixauli, C.; Pascual, B. Effect of deficit irrigation on the productive response of drip-irrigated onion (Allium cepa L.) in mediterranean conditions. Hortic. J. 2019, 88, 488–498. [Google Scholar] [CrossRef] [Green Version]
  9. Farooq, M.; Wahid, A.; Kobayashi, N.; Fujita, D.; Basra, S.M.A. Plant drought stress: Effects, mechanisms and management. Agron. Sustain. Dev. 2009, 29, 185–212. [Google Scholar] [CrossRef] [Green Version]
  10. Fahad, S.; Bajwa, A.A.; Nazir, U.; Anjum, S.A.; Farooq, A.; Zohaib, A.; Sadia, S.; Nasim, W.; Adkins, S.; Saud, S.; et al. Crop production under drought and heat stress: Plant responses and management options. Front. Plant Sci. 2017, 8, 1–16. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Upadhyaya, H.; Sahoo, L.; Panda, S.K. Molecular Physiology of Osmotic Stress in Plants. In Molecular Stress Physiology of Plants; Rout, G.R., Das, A.B., Eds.; Springer: New Delhi, India, 2013; pp. 179–192. ISBN 978-81-322-0807-5. [Google Scholar]
  12. Zhu, J. Abiotic Stress Signaling and Responses in Plants. Cell 2016, 167, 313–324. [Google Scholar] [CrossRef] [Green Version]
  13. Abd El-Mageed, T.A.; Rady, M.M.; Taha, R.S.; Abd El Azeam, S.; Simpson, C.R.; Semida, W.M. Effects of integrated use of residual sulfur-enhanced biochar with effective microorganisms on soil properties, plant growth and short-term productivity of Capsicum annuum under salt stress. Sci. Hortic. 2020, 261, 108930. [Google Scholar] [CrossRef]
  14. Rady, M.M.; Taha, S.S.; Kusvuran, S. Integrative application of cyanobacteria and antioxidants improves common bean performance under saline conditions. Sci. Hortic. 2018, 233, 61–69. [Google Scholar] [CrossRef]
  15. Khalid, A.; Aftab, F. Effect of exogenous application of IAA and GA3 on growth, protein content, and antioxidant enzymes of Solanum tuberosum L. grown in vitro under salt stress. Vitr. Cell. Dev. Biol. Plant 2020, 56, 377–389. [Google Scholar] [CrossRef]
  16. Abd El-Mageed, T.A.; Semida, W.M.; Mohamed, G.F.; Rady, M.M. Combined effect of foliar-applied salicylic acid and deficit irrigation on physiological-anatomical responses, and yield of squash plants under saline soil. S. Afr. J. Bot. 2016, 106, 8–16. [Google Scholar] [CrossRef]
  17. Taha, R.S.; Alharby, H.F.; Bamagoos, A.A.; Medani, R.A.; Rady, M.M. Elevating tolerance of drought stress in Ocimum basilicum using pollen grains extract; a natural biostimulant by regulation of plant performance and antioxidant defense system. S. Afr. J. Bot. 2020, 128, 42–53. [Google Scholar] [CrossRef]
  18. Rady, M.M.; Belal, H.E.E.; Gadallah, F.M.; Semida, W.M. Selenium application in two methods promotes drought tolerance in Solanum lycopersicum plant by inducing the antioxidant defense system. Sci. Hortic. 2020, 266, 109290. [Google Scholar] [CrossRef]
  19. Sitohy, M.Z.; Desoky, E.S.M.; Osman, A.; Rady, M.M. Pumpkin seed protein hydrolysate treatment alleviates salt stress effects on Phaseolus vulgaris by elevating antioxidant capacity and recovering ion homeostasis. Sci. Hortic. 2020, 271, 109495. [Google Scholar] [CrossRef]
  20. Hasanuzzaman, M.; Borhannuddin Bhuyan, M.H.M.; Anee, T.I.; Parvin, K.; Nahar, K.; Al Mahmud, J.; Fujita, M. Regulation of ascorbate-glutathione pathway in mitigating oxidative damage in plants under abiotic stress. Antioxidants 2019, 8, 384. [Google Scholar] [CrossRef] [Green Version]
  21. Turner, N.C. Turgor maintenance by osmotic adjustment: 40 years of progress. J. Exp. Bot. 2018, 69, 3223–3233. [Google Scholar] [CrossRef] [Green Version]
  22. Miceli, A.; Moncada, A.; Sabatino, L.; Vetrano, F. Effect of gibberellic acid on growth, yield, and quality of leaf lettuce and rocket grown in a floating system. Agronomy 2019, 9, 382. [Google Scholar] [CrossRef] [Green Version]
  23. Taiz, L.; Zeiger, E. Plant Physiology, 3rd ed.; Sinauer Associates: Sunderland, MA, USA, 2002; ISBN 0878938230. [Google Scholar]
  24. Ashraf, M.; Karim, F.; Rasul, E. Interactive effects of gibberellic acid (GA3) and salt stress on growth, ion accumulation and photosynthetic capacity of two spring wheat (Triticum aestivum L.) cultivars differing in salt tolerance. Plant Growth Regul. 2002, 36, 49–59. [Google Scholar] [CrossRef]
  25. Iqbal, M.; Ashraf, M. Gibberellic acid mediated induction of salt tolerance in wheat plants: Growth, ionic partitioning, photosynthesis, yield and hormonal homeostasis. Environ. Exp. Bot. 2013, 86, 76–85. [Google Scholar] [CrossRef]
  26. Rady, M.M.; Talaat, N.B.; Abdelhamid, M.T.; Shawky, B.T.; Desoky, E.S.M. Maize (Zea mays L.) grains extract mitigates the deleterious effects of salt stress on common bean (Phaseolus vulgaris L.) growth and physiology. J. Hortic. Sci. Biotechnol. 2019, 94, 777–789. [Google Scholar] [CrossRef]
  27. Al Mahmud, J.; Biswas, P.K.; Nahar, K.; Fujita, M.; Hasanuzzaman, M. Exogenous application of gibberellic acid mitigates drought-induced damage in spring wheat. Acta Agrobot. 2019, 72. [Google Scholar] [CrossRef] [Green Version]
  28. Li, Z.; Lu, G.Y.; Zhang, X.K.; Zou, C.S.; Cheng, Y.; Zheng, P.Y. Improving drought tolerance of germinating seeds by exogenous application of gibberellic acid (GA3) in rapeseed (Brassica napus L.). Seed Sci. Technol. 2010, 38, 432–440. [Google Scholar] [CrossRef]
  29. Hasanuzzaman, M.; Fujita, M.; Oku, H.; Islam, M.T. Plant Tolerance to Environmental Stress: Role of Phytoprotectants; CRC Press: Boca Raton, FL, USA, 2019; Volume 4, ISBN 9781138559172. [Google Scholar]
  30. Verma, V.; Ravindran, P.; Kumar, P.P. Plant hormone-mediated regulation of stress responses. BMC Plant Biol. 2016, 16, 1–10. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  31. Rouphael, Y.; Colla, G. Synergistic Biostimulatory Action: Designing the Next Generation of Plant Biostimulants for Sustainable Agriculture. Front. Plant Sci. 2018, 9, 1–7. [Google Scholar] [CrossRef] [Green Version]
  32. Teklić, T.; Parađiković, N.; Špoljarević, M.; Zeljković, S.; Lončarić, Z.; Lisjak, M. Linking abiotic stress, plant metabolites, biostimulants and functional food. Ann. Appl. Biol. 2020, 1–23. [Google Scholar] [CrossRef]
  33. Lucini, L.; Rouphael, Y.; Cardarelli, M.; Canaguier, R.; Kumar, P.; Colla, G. The effect of a plant-derived biostimulant on metabolic profiling and crop performance of lettuce grown under saline conditions. Sci. Hortic. 2015, 182, 124–133. [Google Scholar] [CrossRef]
  34. Semida, W.M.; Rady, M.M. Presoaking application of propolis and maize grain extracts alleviates salinity stress in common bean (Phaseolus vulgaris L.). Sci. Hortic. 2014, 168, 210–217. [Google Scholar] [CrossRef]
  35. Abd El-Mageed, T.A.; Semida, W.M.; Rady, M.M. Moringa leaf extract as biostimulant improves water use efficiency, physio-biochemical attributes of squash plants under deficit irrigation. Agric. Water Manag. 2017, 193, 46–54. [Google Scholar] [CrossRef]
  36. Desoky, E.S.M.; Elrys, A.S.; Rady, M.M. Integrative moringa and licorice extracts application improves Capsicum annuum fruit yield and declines its contaminant contents on a heavy metals-contaminated saline soil. Ecotoxicol. Environ. Saf. 2019, 169, 50–60. [Google Scholar] [CrossRef]
  37. Di Mola, I.; Cozzolino, E.; Ottaiano, L.; Giordano, M.; Rouphael, Y.; Colla, G.; Mori, M. Effect of Vegetal- and Seaweed Extract-Based Biostimulants on Agronomical and Leaf Quality Traits of Plastic Tunnel-Grown Baby Lettuce under Four Regimes of Nitrogen Fertilization. Agronomy 2019, 9, 571. [Google Scholar] [CrossRef] [Green Version]
  38. Semida, W.M.; Abd El-Mageed, T.A.; Hemida, K.; Rady, M.M. Natural bee-honey based biostimulants confer salt tolerance in onion via modulation of the antioxidant defence system. J. Hortic. Sci. Biotechnol. 2019, 94, 632–642. [Google Scholar] [CrossRef]
  39. Van Oosten, M.J.; Pepe, O.; De Pascale, S.; Silletti, S.; Maggio, A. The role of biostimulants and bioeffectors as alleviators of abiotic stress in crop plants. Chem. Biol. Technol. Agric. 2017, 4, 1–12. [Google Scholar] [CrossRef] [Green Version]
  40. Shin, H.; Ustunol, Z. Carbohydrate composition of honey from different floral sources and their influence on growth of selected intestinal bacteria: An in vitro comparison. Food Res. Int. 2005, 38, 721–728. [Google Scholar] [CrossRef]
  41. Saxena, S.; Gautam, S.; Sharma, A. Physical, biochemical and antioxidant properties of some Indian honeys. Food Chem. 2010, 118, 391–397. [Google Scholar] [CrossRef]
  42. Inés, M.; Craig, A.; Ordoñez, R.; Zampini, C.; Sayago, J.; Bedascarrasbure, E.; Alvarez, A.; Salomón, V.; Maldonado, L. LWT—Food Science and Technology Physico chemical and bioactive properties of honeys from Northwestern Argentina. LWT Food Sci. Technol. 2011, 44, 1922–1930. [Google Scholar] [CrossRef]
  43. Bulgari, R.; Franzoni, G.; Ferrante, A. Biostimulants application in horticultural crops under abiotic stress conditions. Agronomy 2019, 9, 306. [Google Scholar] [CrossRef] [Green Version]
  44. Wang, Z.; Liu, L.; Cheng, C.; Ren, Z.; Xu, S.; Li, X. GAI functions in the plant response to dehydration stress in arabidopsis Thaliana. Int. J. Mol. Sci. 2020, 21, 819. [Google Scholar] [CrossRef] [Green Version]
  45. Osakabe, Y.; Osakabe, K.; Shinozaki, K.; Tran, L.-S.P. Response of plants to water stress. Front. Plant Sci. 2014, 5, 86. [Google Scholar] [CrossRef] [Green Version]
  46. Alzahrani, Y.; Rady, M.M. Compared to antioxidants and polyamines, the role of maize grain-derived organic biostimulants in improving cadmium tolerance in wheat plants. Ecotoxicol. Environ. Saf. 2019, 182, 109378. [Google Scholar] [CrossRef]
  47. Desoky, E.M.; El-maghraby, L.M.M.; Awad, A.E.; Abdo, A.I.; Rady, M.M.; Semida, W.M. Fennel and ammi seed extracts modulate antioxidant defence system and alleviate salinity stress in cowpea (Vigna unguiculata). Sci. Hortic. 2020, 272, 109576. [Google Scholar] [CrossRef]
  48. Sun, T. Gibberellin signal transduction in stem elongation & leaf growth. In Plant Hormones; Davies, P.J., Ed.; Springer: Dordrecht, The Netherlands, 2004; pp. 308–328. ISBN 9781402026867. [Google Scholar]
  49. Azuma, T.; Ueno, S.; Uchida, N.; Yasuda, T. Gibberellin-induced elongation and osmoregulation in internodes of floating rice. Physiol. Plant. 1997, 99, 517–522. [Google Scholar] [CrossRef]
  50. Wood, A.; Paleg, L.G. The Influence of Gibberellic Acid on the Permeability of Model Membrane Systems. Plant Physiol. 1972, 50, 103–108. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  51. Yan, W.; Zhong, Y.; Shangguan, Z. A meta-analysis of leaf gas exchange and water status responses to drought. Sci. Rep. 2016, 6, 1–9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Zhao, H.; Zhang, K.; Zhou, X.; Xi, L.; Wang, Y.; Xu, H.; Pan, T.; Zou, Z. Melatonin alleviates chilling stress in cucumber seedlings by up-regulation of CsZat12 and modulation of polyamine and abscisic acid metabolism. Sci. Rep. 2017, 7, 1–12. [Google Scholar] [CrossRef] [PubMed]
  53. Slabbert, M.M.; Krüger, G.H.J. Antioxidant enzyme activity, proline accumulation, leaf area and cell membrane stability in water stressed Amaranthus leaves. S. Afr. J. Bot. 2014, 95, 123–128. [Google Scholar] [CrossRef] [Green Version]
  54. Guidi, L.; Lo Piccolo, E.; Landi, M. Chlorophyll fluorescence, photoinhibition and abiotic stress: Does it make any difference the fact to be a C3 or C4 species? Front. Plant Sci. 2019, 10, 1–11. [Google Scholar] [CrossRef]
  55. Muhammad, I.; Shalmani, A.; Ali, M.; Yang, Q.-H.; Ahmad, H.; Li, F.B. Mechanisms Regulating the Dynamics of Photosynthesis Under Abiotic Stresses. Front. Plant Sci. 2021, 11, 1–25. [Google Scholar] [CrossRef]
  56. Aktas, L.Y.; Akca, H.; Altun, N.; Battal, P. Phytohormone levels of drought acclimated laurel seedlings in semiarid conditions. Gen. Appl. Plant Physiol. 2008, 34, 203–214. [Google Scholar]
  57. Singh, M.; Kumar, J.; Singh, S.; Singh, V.P.; Prasad, S.M. Roles of osmoprotectants in improving salinity and drought tolerance in plants: A review. Rev. Environ. Sci. Biotechnol. 2015, 14, 407–426. [Google Scholar] [CrossRef]
  58. Munteanu, V.; Gordeev, V.; Martea, R.; Duca, M. Effect of gibberellin cross talk with other phytohormones on cellular growth and mitosis to endoreduplication transition. Int. J. Adv. Res. Biol. Sci. 2014, 1, 1–18. [Google Scholar]
  59. Ullah, A.; Manghwar, H.; Shaban, M.; Khan, A.H.; Akbar, A.; Ali, U.; Ali, E.; Fahad, S. Phytohormones enhanced drought tolerance in plants: A coping strategy. Environ. Sci. Pollut. Res. 2018, 25, 33103–33118. [Google Scholar] [CrossRef] [PubMed]
  60. Kaya, C.; Tuna, A.L.; Alves, A.A.C. Gibberellic acid improves water deficit tolerance in maize plants. Aust. J. Crop Sci. 2006, 28, 331–337. [Google Scholar] [CrossRef]
  61. ElSayed, A.I.; Boulila, M.; Rafudeen, M.S.; Sengupta, S.; Rady, M.M. Melatonin regulatory mechanisms and phylogenetic analyses implying new sequences of melatonin biosynthesis related genes extracted from peanut under salinity stress. Plants 2020, 9, 854. [Google Scholar] [CrossRef] [PubMed]
  62. Seleiman, M.F.; Semida, W.M.; Rady, M.M.; Mohamed, G.F.; Hemida, K.A.; Alhammad, B.A.; Hassan, M.M.; Shami, A. Sequenced Antioxidants Application Rectifies Ion Imbalance and Strengthens Antioxidant Systems in Salt-stressed Cucumber. Plants 2020, 9, 1783. [Google Scholar] [CrossRef]
  63. Taha, R.S.; Seleiman, M.F.; Alotaibi, M.; Alhammad, B.A.; Rady, M.M.; Mahdi, A.H.A. Exogenous potassium treatments elevate salt tolerance and performances of Glycine max by boosting antioxidant defense system under actual saline field conditions. Agronomy 2020, 10, 1741. [Google Scholar] [CrossRef]
  64. Desoky, E.S.; Mansour, E.; Ali, M.M.A.; Yasin, M.A.T.; Abdul-Hamid, M.I.E.; Rady, M.M.; Ali, E.F. Exogenously used 24-epibrassinolide promotes drought tolerance in maize hybrids by improving plant and water productivity in an arid environment. Plants 2021, 10, 354. [Google Scholar] [CrossRef] [PubMed]
  65. Semida, W.M.; Abdelkhalik, A.; Mohamed, G.F.; Abd El-Mageed, T.A.; Abd El-Mageed, S.A.; Rady, M.M.; Ali, E.F. Foliar Application of Zinc Oxide Nanoparticles Promotes Drought Stress Tolerance in Eggplant (Solanum melongena L.). Plants 2021, 10, 421. [Google Scholar] [CrossRef] [PubMed]
  66. Soil Survey Staff USDA. Keys to Soil Taxonomy, 12th ed.; USDA-NRCS: Washington, DC, USA, 2014; ISBN 0926487221.
  67. Klute, A. Methods of Soil Analysis: Part. 1 Physical and Mineralogical Methods, 2nd ed.; The American Society of Agronomy, Inc.: Madison, WI, USA; Soil Science Society of America, Inc.: Madison, WI, USA, 1986. [Google Scholar]
  68. Page, A.L.; Miller, R.H.; Keeney, D.R. Methods of Soil Analysis Part. 2. Chemical and Microbiological Properties; American Society of Agronomy, Inc.: Madison, WI, USA, 1982. [Google Scholar]
  69. Dahnke, W.C.; Whitney, D.A. Measurement of soil salinity. In Recommended Chemical Soil Test Procedures for the North Central Region. North Central Regional Publication 221.; Dahnke, W.C., Ed.; North Dakota Agricultural Experiment Station Bulletin: Fargo, ND, USA, 1988; Volume 499, pp. 32–34. [Google Scholar]
  70. Allen, R.G.; Pereira, L.S.; Raes, D.; Smith, M. Crop Evapotranspiration: Guidelines for Computing Crop Requirements; Irrigation and Drainage Paper No. 56; Food and Agriculture Organization of the United Nations: Rome, Italy, 1988. [Google Scholar]
  71. AOAC. Official methods of analysis of AOAC international. In Association of Official Analysis Chemists International; Horwitz, W., Ed.; AOAC: Rockville, MD, 1995; Volume II, pp. 1058–1059. [Google Scholar]
  72. Bogdanov, S.; Baumann, E. Bestimmung von Honigzuckern mit HPLC. Mitt. Geb. Lebensm. Hyg. 1988, 79, 198–206. [Google Scholar]
  73. Chapman, H.D.; Pratt, P.F. Methods of Analysis for Soil, Plants and Water; Division of Agricultural Science, University of California: Berkeley, CA, USA, 1961; pp. 60–61, 150–179. [Google Scholar]
  74. Mukherjee, S.P.; Choudhuri, M.A. Implications of water stress-induced changes in the levels of endogenous ascorbic acid and hydrogen peroxide in Vigna seedlings. Physiol. Plant. 1983, 58, 166–170. [Google Scholar] [CrossRef]
  75. Lee, S.; Kim, J.; Jeong, S.; Kim, D. Effect of far-infrared radiation on the antioxidant activity of rice hulls. J. Agric. Food Chem. 2003, 51, 4400–4403. [Google Scholar] [CrossRef] [PubMed]
  76. Jensen, M.E. Design and Operation of Farm Irrigation Systems; American Society of Agricultural Engineers: St. Joseph, MI, USA, 1983; p. 827. [Google Scholar]
  77. Arnon, D.I. Copper enzymes in isolated chloroplasts. Polyphenol oxidase in Beta vulgaris L. Plant Physiol. 1949, 24, 1–16. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  78. Jagendorf, A.T. Oxidation and reduction of pyridine nucleotides by purified chloroplasts. Arch. Biochem. Biophys. 1956, 62, 141–150. [Google Scholar] [CrossRef]
  79. Avron, M. Photophosphorylation by Swis- chard chloroplasts chloroplasts. Biochim. Biophys. Acta 1960, 40, 257–272. [Google Scholar] [CrossRef]
  80. Maxwell, K.; Johnson, G.N. Chlorophyll fluorescence—A practical guide. J. Exp. Bot. 2000, 51, 659–668. [Google Scholar] [CrossRef]
  81. Clark, A.J.; Landolt, W.; Bucher, J.B.; Strasser, R.J. Beech (Fagus sylvatica) response to ozone exposure assessed with a chlorophyll a fluorescence performance index. Environ. Pollut. 2000, 109, 501–507. [Google Scholar] [CrossRef]
  82. Osman, A.S.; Rady, M.M. Effect of humic acid as an additive to growing media to enhance the production of eggplant and tomato transplants. J. Hortic. Sci. Biotechnol. 2014, 89, 237–244. [Google Scholar] [CrossRef]
  83. Rady, M.M. Effect of 24-epibrassinolide on growth, yield, antioxidant system and cadmium content of bean (Phaseolus vulgaris L.) plants under salinity and cadmium stress. Sci. Hortic. 2011, 129, 232–237. [Google Scholar] [CrossRef]
  84. Madhava Rao, K.V.; Sresty, T.V.S. Antioxidative parameters in the seedlings of pigeonpea (Cajanus cajan (L.) Millspaugh) in response to Zn and Ni stresses. Plant Sci. 2000, 157, 113–128. [Google Scholar] [CrossRef]
  85. Velikova, V.; Yordanov, I.; Edreva, A. Oxidative stress and some antioxidant systems in acid rain-treated bean plants protective role of exogenous polyamines. Plant Sci. 2000, 151, 59–66. [Google Scholar] [CrossRef]
  86. Kubiś, J. Exogenous spermidine differentially alters activities of some scavenging system enzymes, H2O2 and superoxide radical levels in water-stressed cucumber leaves. J. Plant Physiol. 2008, 165, 397–406. [Google Scholar] [CrossRef]
  87. Bates, L.S.; Waldren, R.P.; Teare, I.D. Rapid determination of free proline for water-stress studies. Plant Soil 1973, 207, 205–207. [Google Scholar] [CrossRef]
  88. Grieve, C.M.; Grattan, S.R. Rapid assay for determination of water soluble quaternary ammonium compounds. Plant Soil 1983, 70, 303–307. [Google Scholar] [CrossRef]
  89. Irigoyen, J.J.; Einerich, D.W.; Sánchez-Díaz, M. Water stress induced changes in concentrations of proline and total soluble sugars in nodulated alfalfa (Medicago sativa) plants. Physiol. Plant. 1992, 84, 55–60. [Google Scholar] [CrossRef]
  90. Bradford, M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 1976, 72, 248–254. [Google Scholar] [CrossRef]
  91. Huang, C.; He, W.; Guo, J.; Chang, X.; Su, P.; Zhang, L. Increased sensitivity to salt stress in an ascorbate-deficient Arabidopsis mutant. J. Exp. Bot. 2005, 56, 3041–3049. [Google Scholar] [CrossRef] [Green Version]
  92. Yu, C.W.; Murphy, T.M.; Lin, C.H. Hydrogen peroxide-induced chilling tolerance in mung beans mediated through ABA-independent glutathione accumulation. Funct. Plant Biol. 2003, 30, 955–963. [Google Scholar] [CrossRef]
  93. Paradiso, A.; Berardino, R.; De Pinto, M.C.; Sanità Di Toppi, L.; Storelli, M.M.; Tommasi, F.; De Gara, L. Increase in ascorbate-glutathione metabolism as local and precocious systemic responses induced by cadmium in durum wheat plants. Plant Cell Physiol. 2008, 49, 362–374. [Google Scholar] [CrossRef] [PubMed]
  94. Ching, L.S.; Mohamed, S. Alpha-tocopherol content in 62 edible tropical plants. J. Agric. Food Chem. 2001, 49, 3101–3105. [Google Scholar] [CrossRef] [PubMed]
  95. Konings, E.J.M.; Roomans, H.H.S.; Beljaars, P.R. Liquid Chromatographic Determination of Tocopherols and Tocotrienols in Margarine, Infant Foods, and Vegetables. J. AOAC Int. 1996, 79, 902–906. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  96. Makkar, H.P.S.; Becker, K.; Abel, H.; Pawelzik, E. Nutrient contents, rumen protein degradability and antinutritional factors in some colour- and white-flowering cultivars of Vicia faba beans. J. Sci. Food Agric. 1997, 75, 511–520. [Google Scholar] [CrossRef]
  97. Aebi, H. Catalase in Vitro. Methods Enzymol. 1984, 105, 121–126. [Google Scholar] [CrossRef]
  98. Nakano, Y.; Asada, K. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol. 1981, 22, 867–880. [Google Scholar] [CrossRef]
  99. Foster, J.G.; Hess, J.L. Responses of Superoxide Dismutase and Glutathione Reductase Activities in Cotton Leaf Tissue Exposed to an Atmosphere Enriched in Oxygen. Plant Physiol. 1980, 66, 482–487. [Google Scholar] [CrossRef]
  100. Yu, Q.; Rengel, Z. Drought and salinity differentially influence activities of superoxide dismutases in narrow-leafed lupins. Plant Sci. 1999, 142, 1–11. [Google Scholar] [CrossRef]
  101. AOAC. Official Methods of Analysis of the Association of Official Agricultural Chemists, 6th ed.; AOAC: Washington, DC, USA, 1995. [Google Scholar]
  102. Jackson, M.L. Soil Chemical Analysis; Prentice Hall of India Pvt. Ltd.: New Delhi, India, 1967. [Google Scholar]
  103. Johnson, C.M.; Ulrich, A. Analytical Methods for Use in Plant Analysis; Bulletin (Agricultural Experiment Station, Berkeley, Calif.); University of California: Berkeley, CA, USA, 1959. [Google Scholar]
  104. Nehela, Y.; Hijaz, F.; Elzaawely, A.A.; El-Zahaby, H.M.; Killiny, N. Phytohormone profiling of the sweet orange (Citrus sinensis (L.) Osbeck) leaves and roots using GC-MS-based method. J. Plant Physiol. 2016, 199, 12–17. [Google Scholar] [CrossRef] [PubMed]
  105. Ünyayar, S.; Topcuoglu, S.F.; Ünyayar, A. A modified method for extraction and identification of indole-3-acetic acid (IAA), gibberellic acid (GA3), abscisic acid (ABA) and zeatin produced by Phanerochaete chrysosporium ME446. Bulg. J. Plant Physiol. 1996, 22, 105–110. [Google Scholar]
Table
Table 1. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted growth and green pod yield components of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Table 1. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted growth and green pod yield components of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Source of VariationNo. of Leaves per PlantLeaf Area per Plant (cm2)Shoot DW per Plant (g)No. of Green Pods per PlantGreen Pods Yield per Hectare (ton)WUE (Kg per m3)
Season of 2018/2019
Irrigation (Ir)********
100% of ETc31.8 ± 3.1a136.0 ± 13.7a17.7 ± 1.7a20.2 ± 1.7a32.5 ± 2.9a8.81 ± 1.12a
60% of ETc24.8 ± 2.4b100.7 ± 10.1b10.4 ± 1.0b14.2 ± 1.3b16.8 ± 1.7b7.59 ± 1.09b
Regulators (Re)******
Control (Cn)23.5 ± 2.3c95.0 ± 10.3c10.1 ± 1.0c13.3 ± 1.3c15.1 ± 1.5c5.12 ± 0.88c
GA329.7 ± 3.0b125.8 ± 12.6b15.0 ± 1.6b18.2 ± 1.4b26.9 ± 2.3b9.11 ± 1.03b
Db-H31.7 ± 3.0a134.3 ± 12.9a17.2 ± 1.6a20.0 ± 1.9a32.1 ± 3.1a10.87 ± 1.21a
Ir × Re******
100% ETc × Cn 28.3 ± 2.7c117.5 ± 12.1c11.9 ± 1.2c16.5 ± 1.3c20.8 ± 1.8c5.64 ± 0.98d
100% ETc × GA331.7 ± 3.4b137.7 ± 14.2b18.5 ± 1.9b20.3 ± 1.5b33.3 ± 2.4b9.02 ± 1.13b
100% ETc × Db-H35.3 ± 3.2a152.7 ± 14.8a22.7 ± 2.1a23.7 ± 2.4a43.5 ± 4.4a11.79 ± 1.23a
60% ETc × Cn18.7 ± 1.9c72.4 ± 8.4d8.2 ± 0.7d10.1 ± 1.3d9.4 ± 1.1d4.25 ± 0.86c
60% ETc × GA327.7 ± 2.6c113.8 ± 11.0c11.4 ± 1.2c16.1 ± 1.3c20.4 ± 2.1c9.21 ± 0.99b
60% ETc × Db-H28.0 ± 2.8c115.9 ± 10.9c11.7 ± 1.0c16.3 ± 1.4c20.7 ± 1.8c9.35 ± 1.21b
Season of 2019/2020
Irrigation (Ir)********
100% of ETc33.1 ± 3.2a152.4 ± 13.3a19.8 ± 2.0a19.1 ± 2.2a31.2 ± 3.1a8.31 ± 0.93a
60% of ETc25.6 ± 2.4b113.9 ± 11.1b11.2 ± 1.0b13.5 ± 1.5b17.2 ± 1.7b7.64 ± 1.02b
Regulators (Re)******
Control (Cn)24.2 ± 2.4b105.6 ± 9.3c10.7 ± 1.1c12.6 ± 1.4c15.2 ± 1.7c5.06 ± 1.03c
GA331.0 ± 3.0a140.8 ± 12.3b17.2 ± 1.8b17.3 ± 2.0b26.6 ± 2.6b8.86 ± 1.16b
Db-H33.0 ± 3.2a151.4 ± 15.1a18.7 ± 1.7a19.2 ± 2.2a30.9 ± 3.1a10.29 ± 1.32a
Ir × Re******
100% ETc × Cn 29.4 ± 2.8c134.1 ± 10.4c12.7 ± 1.3c15.9 ± 1.8c21.8 ± 2.3c5.81 ± 0.69d
100% ETc × GA333.1 ± 3.2b150.2 ± 12.2b21.9 ± 2.2b18.8 ± 2.2b31.7 ± 2.8b8.44 ± 1.06c
100% ETc × Db-H36.7 ± 3.7a169.4 ± 17.4a24.8 ± 2.3a22.7 ± 2.5a40.1 ± 4.2a10.68 ± 1.22a
60% ETc × Cn18.9 ± 1.9d77.1 ± 8.2d8.7 ± 0.9d9.2 ± 1.0d8.5 ± 1.0d3.77 ± 0.63e
60% ETc × GA328.8 ± 2.7c131.4 ± 12.4c12.4 ± 1.2c15.7 ± 1.7c21.4 ± 2.3c9.50 ± 1.11b
60% ETc × Db-H29.2 ± 2.6c133.3 ± 12.7c12.6 ± 1.0c15.7 ± 1.8c21.7 ± 1.9c9.63 ± 1.13b
** and * indicate respectively differences at p ≤ 0.05 and p ≤ 0.01 probability level. Means followed by the same letter in each column are not significantly different according to the LSD test (p ≤ 0.05).
Table
Table 2. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted photosynthetic machinery efficiency of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Table 2. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted photosynthetic machinery efficiency of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Source of VariationTotal Chlorophylls (mg per g FW)Total Carotenoids (mg per g FW)Photochemical ActivitySPAD Chlorophyll IndexFv/FmPerformance Index (%)
Season of 2018/2019
Irrigation (Ir)******
100% of ETc3.13 ± 0.19a0.75 ± 0.02a45.2 ± 1.6a66.6 ± 2.4a0.85 ± 0.02a16.8 ± 0.21a
60% of ETc2.44 ± 0.12b0.63 ± 0.01b38.9 ± 1.3b56.8 ± 1.9b0.77 ± 0.02b13.8 ± 0.17b
Regulators (Re)******
Control (Cn)2.33 ± 0.12c0.60 ± 0.01c37.5 ± 1.2b54.0 ± 1.8b0.75 ± 0.02b13.0 ± 0.18c
GA32.94 ± 0.19b0.72 ± 0.02b43.7 ± 1.6a64.7 ± 2.5a0.83 ± 0.03a16.0 ± 0.19b
Db-H3.10 ± 0.15a0.76 ± 0.02a45.0 ± 1.7a66.4 ± 2.2c0.86 ± 0.03a17.1 ± 0.22a
Ir × Re******
100% ETc × Cn 2.78 ± 0.17c0.68 ± 0.01c42.3 ± 1.3b62.4 ± 2.1c0.81 ± 0.02b15.8 ± 0.21b
100% ETc× GA33.18 ± 0.21b0.76 ± 0.02b45.4 ± 1.6a67.1 ± 2.7a0.85 ± 0.02ab16.3 ± 0.18b
100% ETc × Db-H3.42 ± 0.18a0.82 ± 0.02a47.9 ± 2.0a70.2 ± 2.4a0.89 ± 0.03a18.4 ± 0.25a
60% ETc × Cn1.87 ± 0.07d0.52 ± 0.00d32.6 ± 1.1c45.6 ± 1.4d0.69 ± 0.01c10.1 ± 0.14c
60% ETc × GA32.69 ± 0.16c0.68 ± 0.01c41.9 ± 1.5b62.3 ± 2.2c0.80 ± 0.03b15.6 ± 0.20b
60% ETc × Db-H2.77 ± 0.12c0.70 ± 0.02c42.1 ± 1.3b62.5 ± 2.0c0.82 ± 0.02b15.7 ± 0.18b
Season of 2019/2020
Irrigation (Ir)******
100% of ETc3.41 ± 0.14a0.76 ± 0.03a46.1 ± 1.6a68.2 ± 2.2a0.85 ± 0.03a17.2 ± 0.17a
60% of ETc2.60 ± 0.11b0.65 ± 0.01b39.2 ± 1.5b57.1 ± 2.0b0.75 ± 0.02b13.7 ± 0.13b
Regulators (Re)******
Control (Cn)2.38 ± 0.10b0.63 ± 0.01b37.5 ± 1.5b53.9 ± 2.1b0.73 ± 0.02b12.9 ± 0.14b
GA33.26 ± 0.13a0.73 ± 0.02a44.6 ± 1.8a65.7 ± 2.0a0.83 ± 0.02a16.3 ± 0.16a
Db-H3.40 ± 0.14a0.76 ± 0.03a46.0 ± 1.6a68.3 ± 2.3a0.85 ± 0.04a17.2 ± 0.16a
Ir × Re******
100% ETc × Cn 3.01 ± 0.12b0.70 ± 0.02b43.1 ± 1.5b63.5 ± 2.4b0.80 ± 0.03b15.5 ± 0.16c
100% ETc× GA33.49 ± 0.15a0.76 ± 0.02a46.4 ± 1.8a68.1 ± 1.9a0.86 ± 0.02a17.1 ± 0.18b
100% ETc × Db-H3.74 ± 0.14a0.81 ± 0.04a48.9 ± 1.6a72.9 ± 2.2a0.89 ± 0.04a19.0 ± 0.18a
60% ETc × Cn1.74 ± 0.08c0.56 ± 0.00c31.8 ± 1.4c44.3 ± 1.7c0.66 ± 0.01c10.3 ± 0.11d
60% ETc × GA33.02 ± 0.11b0.69 ± 0.02b42.8 ± 1.7b63.3 ± 2.1b0.79 ± 0.02b15.4 ± 0.14c
60% ETc × Db-H3.05 ± 0.14b0.71 ± 0.02b43.0 ± 1.5b63.6 ± 2.3b0.80 ± 0.04b15.4 ± 0.14c
** and * indicate respectively differences at p ≤ 0.05 and p ≤ 0.01 probability level. Means followed by the same letter in each column are not significantly different according to the LSD test (p ≤ 0.05).
Table
Table 3. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted leaf tissue stability and levels of oxidative stress biomarkers in Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Table 3. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted leaf tissue stability and levels of oxidative stress biomarkers in Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Source of VariationRelative Water Content (%)Membrane Stability Index (%)Electrolyte Leakage (%)Malondialdehyde Level (µmole per g FW)Hydrogen Peroxide (H2O2) Level (µmole per g FW)Superoxide (O2•‒) Level (µmole per g FW)
Season of 2018/2019
Irrigation (Ir)**********
100% of ETc87.6 ± 4.6a76.3 ± 3.8a10.6 ± 0.5b0.12 ± 0.01b1.29 ± 0.03b0.50 ± 0.01b
60% of ETc74.0 ± 4.3b61.2 ± 3.3b18.9 ± 1.0a0.20 ± 0.01a2.04 ± 0.02a1.01 ± 0.02a
Regulators (Re)******
Control (Cn)70.5 ± 3.8b55.6 ± 3.3b22.4 ± 1.3a0.24 ± 0.02a2.29 ± 0.05a1.22 ± 0.03a
GA385.2 ± 4.7a75.1 ± 3.8a11.0 ± 0.6b0.13 ± 0.01b1.37 ± 0.02b0.53 ± 0.02b
Db-H86.8 ± 4.9a75.5 ± 3.6a10.8 ± 0.5b0.12 ± 0.00b1.34 ± 0.02b0.52 ± 0.01b
Ir × Re******
100% ETc × Cn 82.6 ± 4.5b72.8 ± 3.3b11.1 ± 0.6b0.13 ± 0.01b1.46 ± 0.04b0.55 ± 0.02b
100% ETc × GA388.9 ± 4.2a77.9 ± 4.1a10.4 ± 0.6b0.12 ± 0.01b1.21 ± 0.02c0.48 ± 0.01c
100% ETc × Db-H91.4 ± 5.1a78.1 ± 3.9a10.2 ± 0.4b0.12 ± 0.00b1.19 ± 0.02c0.47 ± 0.01c
60% ETc × Cn58.3 ± 3.0c38.4 ± 3.2c33.7 ± 2.0a0.34 ± 0.02a3.11 ± 0.06a1.88 ± 0.04a
60% ETc × GA381.4 ± 5.1b72.2 ± 3.4b11.6 ± 0.5b0.14 ± 0.01b1.52 ± 0.02b0.57 ± 0.02b
60% ETc × Db-H82.2 ± 4.7b72.9 ± 3.3b11.3 ± 0.6b0.12 ± 0.00b1.48 ± 0.02b0.57 ± 0.01b
Season of 2019/2020
Irrigation (Ir)**********
100% of ETc88.3 ± 5.1a76.2 ± 3.7a10.4 ± 0.4b0.12 ± 0.00b1.36 ± 0.09b0.44 ± 0.02a
60% of ETc74.5 ± 4.0b61.0 ± 3.9b17.8 ± 0.7a0.20 ± 0.01a2.18 ± 0.11a0.88 ± 0.04a
Regulators (Re)******
Control (Cn)70.5 ± 4.3b55.8 ± 4.0b21.5 ± 0.9a0.27 ± 0.02a2.48 ± 0.15a1.06 ± 0.06a
GA386.1 ± 4.7a74.8 ± 4.0a10.6 ± 0.5b0.12 ± 0.01b1.45 ± 0.10b0.47 ± 0.02b
Db-H87.7 ± 4.8a75.3 ± 3.5a10.4 ± 0.3b0.11 ± 0.00b1.37 ± 0.06b0.46 ± 0.02b
Ir × Re******
100% ETc × Cn 83.7 ± 5.1b71.4 ± 3.3b10.8 ± 0.3b0.15 ± 0.01b1.55 ± 0.08b0.49 ± 0.03b
100% ETc× GA389.4 ± 4.8a78.2 ± 4.1a10.4 ± 0.5b0.11 ± 0.00cd1.30 ± 0.12c0.42 ± 0.02c
100% ETc × Db-H91.8 ± 5.4a78.9 ± 3.8a10.1 ± 0.3b0.11 ± 0.00cd1.22 ± 0.07c0.41 ± 0.02c
60% ETc × Cn57.2 ± 3.4c40.1 ± 4.6c32.1 ± 1.4a0.38 ± 0.02a3.41 ± 0.21a1.62 ± 0.09a
60% ETc × GA382.8 ± 4.6b71.3 ± 3.8b10.7 ± 0.5b0.12 ± 0.01c1.60 ± 0.07b0.52 ± 0.02b
60% ETc × Db-H83.6 ± 4.1b71.6 ± 3.2b10.7 ± 0.3b0.10 ± 0.00d1.52 ± 0.05b0.50 ± 0.01b
** and * indicate respectively differences at p ≤ 0.05 and p ≤ 0.01 probability level. Means followed by the same letter in each column are not significantly different according to the LSD test (p ≤ 0.05).
Table
Table 4. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted osmoprotectant contents of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Table 4. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted osmoprotectant contents of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Source of VariationSoluble Sugars (mg per g DW)Free Proline (µM per g W)Glycine Betaine (µM per g DW)Total Soluble Protein (mg per g DW)
Season of 2018/2019
Irrigation (Ir)******
100% of ETc14.1 ± 0.3b138.5 ± 1.8b22.4 ± 0.4b72.1 ± 1.5b
60% of ETc19.9 ± 0.4a221.5 ± 2.5a41.4 ± 0.7a88.6 ± 1.9a
Regulators (Re)****
Control (Cn)14.0 ± 0.3c154.4 ± 1.6b26.6 ± 0.5b85.4 ± 1.8a
GA317.1 ± 0.4b192.2 ± 2.6a34.3 ± 0.6a78.1 ± 1.8b
Db-H20.1 ± 0.5a193.5 ± 2.3a34.9 ± 0.7a77.6 ± 1.5b
Ir × Re****
100% ETc × Cn 10.4 ± 0.2e114.2 ± 1.5d18.1 ± 0.3d71.8 ± 1.5c
100% ETc× GA314.2 ± 0.4d149.3 ± 2.0c24.3 ± 0.4c72.0 ± 1.7c
100% ETc × Db-H17.8 ± 0.4c152.1 ± 1.8c24.8 ± 0.6c72.4 ± 1.3c
60% ETc × Cn17.5 ± 0.3c194.6 ± 1.7b35.1 ± 0.6b98.9 ± 2.0a
60% ETc × GA319.9 ± 0.4b235.1 ± 3.1a44.2 ± 0.7a84.2 ± 1.9b
60% ETc × Db-H22.3 ± 0.5a234.9 ± 2.8a45.0 ± 0.7a82.7 ± 1.7b
Season of 2019/2020
Irrigation (Ir)*******
100% of ETc17.2 ± 0.4b145.5 ± 2.2b20.8 ± 0.3b73.9 ± 1.6b
60% of ETc24.8 ± 0.5a245.5 ± 3.2a38.5 ± 0.6a87.6 ± 1.8a
Regulators (Re)****
Control (Cn)17.1 ± 0.4c167.0 ± 2.5b23.9 ± 0.4b85.6 ± 1.8a
GA321.3 ± 0.5b209.0 ± 3.0a32.5 ± 0.5a78.6 ± 1.7b
Db-H24.6 ± 0.6a210.6 ± 2.7a32.6 ± 0.5a78.1 ± 1.6b
Ir × Re****
100% ETc × Cn 12.1 ± 0.3e121.4 ± 2.0d16.4 ± 0.2d73.5 ± 1.7c
100% ETc× GA318.0 ± 0.5d158.3 ± 2.5c23.1 ± 0.4c73.9 ± 1.6c
100% ETc × Db-H21.4 ± 0.5c156.8 ± 2.2c22.8 ± 0.3c74.2 ± 1.4c
60% ETc × Cn22.1 ± 0.4c212.6 ± 2.9b31.3 ± 0.5b97.6 ± 1.9a
60% ETc × GA324.6 ± 0.4b259.7 ± 3.4a41.8 ± 0.6a83.2 ± 1.8b
60% ETc × Db-H27.8 ± 0.6a264.3 ± 3.2a42.3 ± 0.6a81.9 ± 1.8b
** and * indicate respectively differences at p ≤ 0.05 and p ≤ 0.01 probability level. Means followed by the same letter in each column are not significantly different according to the LSD test (p ≤ 0.05).
Table
Table 5. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted non-enzymatic antioxidant contents of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Table 5. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted non-enzymatic antioxidant contents of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Source of VariationAscorbate (µM per g FW)Glutathione (µM per g FW)α-Tocopherol (µM per g DW)Total Phenolic Compounds (mg GAE per g DW)
Season of 2018/2019
Irrigation (Ir)*****
100% of ETc1.59 ± 0.03b0.88 ± 0.02b2.22 ± 0.04b8.10 ± 0.27b
60% of ETc2.28 ± 0.04a1.49 ± 0.03a3.10 ± 0.05a10.08 ± 0.32a
Regulators (Re)****
Control (Cn)1.69 ± 0.03c0.98 ± 0.02c2.39 ± 0.04c10.27 ± 0.35a
GA31.99 ± 0.04b1.22 ± 0.03b2.72 ± 0.04b8.86 ± 0.28b
Db-H2.14 ± 0.04a1.36 ± 0.03a2.88 ± 0.05a8.15 ± 0.26c
Ir × Re****
100% ETc × Cn 1.23 ± 0.02e0.64 ± 0.01e1.89 ± 0.03e8.12 ± 0.30c
100% ETc× GA31.64 ± 0.03d0.89 ± 0.02d2.24 ± 0.04d8.10 ± 0.26c
100% ETc × Db-H1.91 ± 0.03c1.11 ± 0.02c2.53 ± 0.05c8.09 ± 0.24c
60% ETc × Cn2.14 ± 0.04b1.32 ± 0.03b2.88 ± 0.05b12.42 ± 0.39a
60% ETc × GA32.33 ± 0.04a1.55 ± 0.04a3.19 ± 0.04a9.62 ± 0.30b
60% ETc × Db-H2.36 ± 0.04a1.60 ± 0.03a3.23 ± 0.05a8.21 ± 0.27c
Season of 2019/2020
Irrigation (Ir)******
100% of ETc1.47 ± 0.02b0.80 ± 0.01b2.39 ± 0.05b7.88 ± 0.20b
60% of ETc2.26 ± 0.05a1.43 ± 0.03a3.37 ± 0.07a9.85 ± 0.25a
Regulators (Re)****
Control (Cn)1.58 ± 0.03c0.95 ± 0.02c2.56 ± 0.05c10.05 ± 0.27a
GA31.93 ± 0.04b1.16 ± 0.02b2.94 ± 0.06b8.68 ± 0.23b
Db-H2.09 ± 0.05a1.25 ± 0.02a3.15 ± 0.07a7.88 ± 0.18c
Ir × Re****
100% ETc × Cn 1.19 ± 0.01e0.66 ± 0.01e1.98 ± 0.04e7.89 ± 0.21c
100% ETc× GA31.44 ± 0.02d0.79 ± 0.01d2.41 ± 0.04d7.91 ± 0.19c
100% ETc × Db-H1.79 ± 0.04c0.94 ± 0.01c2.79 ± 0.06c7.85 ± 0.20c
60% ETc × Cn1.97 ± 0.04b1.23 ± 0.02b3.14 ± 0.06b12.20 ± 0.32a
60% ETc × GA32.41 ± 0.05a1.52 ± 0.03a3.47 ± 0.07a9.44 ± 0.26b
60% ETc × Db-H2.39 ± 0.06a1.55 ± 0.03a3.51 ± 0.08a7.91 ± 0.16c
** and * indicate respectively differences at p ≤ 0.05 and p ≤ 0.01 probability level. Means followed by the same letter in each column are not significantly different according to the LSD test (p ≤ 0.05).
Table
Table 6. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted antioxidant enzyme activities of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Table 6. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted antioxidant enzyme activities of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Source of VariationSuperoxide Dismutase (A564 per min per g Protein)Catalase (A290 per min per g Protein)Glutathione Reductase (A340 per min per g Protein)Ascorbate Peroxidase (A290 per min per g Protein)
Season of 2018/2019
Irrigation (Ir)*******
100% of ETc15.5 ± 0.2b56.5 ± 0.7b23.4 ± 0.3b68.4 ± 0.8b
60% of ETc23.4 ± 0.4a85.5 ± 0.8a37.1 ± 0.4a93.2 ± 0.7a
Regulators (Re)****
Control (Cn)16.7 ± 0.3b63.4 ± 0.7b26.6 ± 0.3b71.6 ± 0.7b
GA320.9 ± 0.3a75.3 ± 0.8a32.2 ± 0.4a85.4 ± 0.8a
Db-H20.8 ± 0.3a74.3 ± 0.8a32.1 ± 0.4a85.4 ± 0.7a
Ir × Re****
100% ETc × Cn 14.1 ± 0.2d48.5 ± 0.6d19.8 ± 0.2d62.1 ± 0.8d
100% ETc× GA316.4 ± 0.2c61.2 ± 0.8c25.1 ± 0.3c71.6 ± 0.8c
100% ETc × Db-H16.0 ± 0.2c59.8 ± 0.7c25.4 ± 0.3c71.4 ± 0.7c
60% ETc × Cn19.2 ± 0.4b78.3 ± 0.8b33.3 ± 0.3b81.1 ± 0.6b
60% ETc × GA325.4 ± 0.3a89.4 ± 0.8a39.2 ± 0.5a99.2 ± 0.8a
60% ETc × Db-H25.6 ± 0.4a88.7 ± 0.9a38.8 ± 0.5a99.3 ± 0.7a
Season of 2019/2020
Irrigation (Ir)*******
100% of ETc17.3 ± 0.3b52.9 ± 0.5b24.2 ± 0.3b64.5 ± 0.7b
60% of ETc27.4 ± 0.4a80.1 ± 0.8a38.4 ± 0.5a85.4 ± 1.0a
Regulators (Re)****
Control (Cn)20.1 ± 0.3b58.3 ± 0.7b27.1 ± 0.4b69.2 ± 0.8b
GA323.4 ± 0.4a70.7 ± 0.8a33.8 ± 0.5a77.9 ± 0.9a
Db-H23.7 ± 0.4a70.7 ± 0.6a33.1 ± 0.4a78.0 ± 0.8a
Ir × Re****
100% ETc × Cn 15.6 ± 0.2d44.2 ± 0.5d21.0 ± 0.3d59.7 ± 0.7d
100% ETc× GA318.1 ± 0.3c57.1 ± 0.6c26.2 ± 0.3c66.8 ± 0.6c
100% ETc × Db-H18.3 ± 0.3c57.4 ± 0.5c25.4 ± 0.2c67.1 ± 0.7c
60% ETc × Cn24.5 ± 0.3b72.3 ± 0.8b33.1 ± 0.4b78.6 ± 0.9b
60% ETc × GA328.7 ± 0.4a84.2 ± 0.9a41.3 ± 0.6a88.9 ± 1.1a
60% ETc × Db-H29.0 ± 0.5a83.9 ± 0.7a40.7 ± 0.5a88.8 ± 0.9a
** and * indicate respectively differences at p ≤ 0.05 and p ≤ 0.01 probability level. Means followed by the same letter in each column are not significantly different according to the LSD test (p ≤ 0.05).
Table
Table 7. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted nutrient contents of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Table 7. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted nutrient contents of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Source of VariationNitrogen (mg per g Dry Weight)Phosphorus (mg per g Dry Weight)Potassium (mg per g Dry Weight)Iron (mg per g Dry Weight)Manganese (mg per g Dry Weight)Zinc (mg per g Dry Weight)
Season of 2018/2019
Irrigation (Ir)******
100% of ETc19.3 ± 1.2a2.51 ± 0.14a19.0 ± 1.3a0.77 ± 0.03a0.50 ± 0.01a0.33 ± 0.01a
60% of ETc15.3 ± 1.3b1.95 ± 0.10b16.3 ± 1.0b0.61 ± 0.01b0.41 ± 0.01b0.26 ± 0.01b
Regulators (Re)******
Control (Cn)14.5 ± 1.1c1.81 ± 0.10c14.6 ± 1.0c0.59 ± 0.02c0.38 ± 0.01c0.24 ± 0.00c
GA318.2 ± 1.2b2.37 ± 0.11b18.2 ± 1.1b0.71 ± 0.02b0.48 ± 0.01b0.31 ± 0.01b
Db-H19.4 ± 1.5a2.51 ± 0.15a20.3 ± 1.5a0.77 ± 0.03a0.52 ± 0.02a0.35 ± 0.01a
Ir × Re******
100% ETc × Cn 16.8 ± 0.9c2.10 ± 0.12c17.2 ± 1.1c0.68 ± 0.02c0.44 ± 0.01c0.29 ± 0.00c
100% ETc× GA319.7 ± 1.2b2.56 ± 0.12b18.9 ± 1.2b0.76 ± 0.02b0.49 ± 0.01b0.33 ± 0.01b
100% ETc × Db-H21.5 ± 1.5a2.88 ± 0.17a20.9 ± 1.7a0.88 ± 0.04a0.57 ± 0.02a0.38 ± 0.01a
60% ETc × Cn12.1 ± 1.3d1.52 ± 0.07d11.9 ± 0.8d0.50 ± 0.01d0.31 ± 0.00d0.18 ± 0.00d
60% ETc × GA316.7 ± 1.2c2.18 ± 0.10c17.4 ± 0.9c0.66 ± 0.01c0.46 ± 0.01c0.28 ± 0.01c
60% ETc × Db-H17.2 ± 1.4c2.14 ± 0.12c19.6 ± 1.2b0.66 ± 0.01c0.47 ± 0.01c0.31 ± 0.01b
Season of 2019/2020
Irrigation (Ir)******
100% of ETc20.2 ± 0.9a2.41 ± 0.11a20.9 ± 1.0a0.80 ± 0.02a0.57 ± 0.01a0.36 ± 0.00a
60% of ETc15.9 ± 0.6b1.84 ± 0.09b15.9 ± 0.8b0.65 ± 0.01b0.44 ± 0.00b0.29 ± 0.00b
Regulators (Re)******
Control (Cn)14.7 ± 0.6c1.70 ± 0.07c14.8 ± 0.8c0.61 ± 0.01c0.41 ± 0.00c0.27 ± 0.00c
GA318.9 ± 0.7b2.22 ± 0.11b18.9 ± 1.0b0.75 ± 0.02b0.53 ± 0.01b0.34 ± 0.00b
Db-H20.7 ± 1.0a2.45 ± 0.13a21.6 ± 1.0a0.83 ± 0.02a0.58 ± 0.01a0.37 ± 0.01a
Ir × Re******
100% ETc × Cn 17.4 ± 0.8c1.98 ± 0.09c16.9 ± 0.9c0.71 ± 0.01c0.50 ± 0.00c0.31 ± 0.00c
100% ETc× GA319.9 ± 0.8b2.42 ± 0.11b20.4 ± 0.9b0.78 ± 0.02b0.56 ± 0.01b0.36 ± 0.00b
100% ETc × Db-H23.4 ± 1.1a2.83 ± 0.14a25.3 ± 1.2a0.91 ± 0.02a0.64 ± 0.01a0.42 ± 0.01a
60% ETc × Cn11.9 ± 0.4d1.42 ± 0.05d12.6 ± 0.6d0.50 ± 0.00d0.32 ± 0.00d0.22 ± 0.00d
60% ETc × GA317.8 ± 0.6c2.02 ± 0.10c17.4 ± 1.0c0.72 ± 0.01c0.49 ± 0.00c0.32 ± 0.00c
60% ETc × Db-H17.9 ± 0.9c2.07 ± 0.12c17.8 ± 0.8c0.74 ± 0.01bc0.51 ± 0.01c0.32 ± 0.00c
** and * indicate respectively differences at p ≤ 0.05 and p ≤ 0.01 probability level. Means followed by the same letter in each column are not significantly different according to the LSD test (p ≤ 0.05).
Table
Table 8. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted plant hormonal contents of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Table 8. Foliar application of some growth regulators (e.g., gibberellic acid; GA3 and diluted bee honey; Db-H) promoted plant hormonal contents of Vicia faba plants grown under well watering (100% of crop evapotranspiration; ETc) or deficit irrigation (60% of ETc).
Source of VariationIndole-3-Acetic Acid (µg per g FW)Gibberellic Acid (µg per g FW)Cytokinins (µg per g FW)Abscisic Acid (µg per g FW)
Season of 2018/2019
Irrigation (Ir)****
100% of ETc18.1 ± 0.15a33.1 ± 0.29a24.6 ± 0.18a4.23 ± 0.05b
60% of ETc14.2 ± 0.14b25.1 ± 0.26b18.4 ± 0.16b6.29 ± 0.06a
Regulators (Re)*****
Control (Cn)12.2 ± 0.10c18.5 ± 0.20c15.5 ± 0.13c7.43 ± 0.07a
GA316.0 ± 0.15b41.9 ± 0.40a22.0 ± 0.18b4.45 ± 0.05b
Db-H20.4 ± 0.19a26.9 ± 0.23b27.2 ± 0.21a3.91 ± 0.05c
Ir × Re****
100% ETc × Cn 14.1 ± 0.11c22.4 ± 0.19d18.7 ± 0.15c5.22 ± 0.06b
100% ETc× GA317.4 ± 0.15b45.6 ± 0.39a25.4 ± 0.20b3.77 ± 0.04e
100% ETc × Db-H22.9 ± 0.19a31.2 ± 0.28c29.8 ± 0.20a3.69 ± 0.04e
60% ETc × Cn10.3 ± 0.09d14.6 ± 0.20e12.2 ± 0.11d9.64 ± 0.07a
60% ETc × GA314.5 ± 0.15c38.2 ± 0.41b18.5 ± 0.15c5.12 ± 0.06c
60% ETc × Db-H17.9 ± 0.18b22.6 ± 0.18d24.6 ± 0.22b4.12 ± 0.05d
Season of 2019/2020
Irrigation (Ir)*****
100% of ETc20.4 ± 0.18a33.9 ± 0.29a24.2 ± 0.20a3.75 ± 0.04b
60% of ETc15.8 ± 0.14b24.7 ± 0.22b18.2 ± 0.19b6.29 ± 0.07a
Regulators (Re)*****
Control (Cn)14.1 ± 0.13c17.6 ± 0.20c15.0 ± 0.14c7.47 ± 0.08a
GA318.1 ± 0.15b44.4 ± 0.37a20.9 ± 0.19b4.19 ± 0.05b
Db-H22.3 ± 0.20a26.0 ± 0.21b27.7 ± 0.26a3.40 ± 0.04c
Ir × Re****
100% ETc × Cn 16.8 ± 0.18c21.6 ± 0.22d17.6 ± 0.12c4.98 ± 0.05b
100% ETc× GA319.7 ± 0.17b50.2 ± 0.45a23.8 ± 0.25b3.48 ± 0.03c
100% ETc × Db-H24.8 ± 0.19a29.8 ± 0.21c31.2 ± 0.22a2.78 ± 0.03d
60% ETc × Cn11.3 ± 0.08d13.6 ± 0.18e12.4 ± 0.15d9.96 ± 0.11a
60% ETc × GA316.4 ± 0.12c38.5 ± 0.29b18.0 ± 0.13c4.89 ± 0.06b
60% ETc × Db-H19.7 ± 0.21b22.1 ± 0.20d24.2 ± 0.30b4.01 ± 0.04c
** and * indicate respectively differences at p ≤ 0.05 and p ≤ 0.01 probability level. Means followed by the same letter in each column are not significantly different according to the LSD test (p ≤ 0.05).
Table
Table 9. Some initial physical and chemical soil properties.
Table 9. Some initial physical and chemical soil properties.
Layer (cm)Particle Size DistributionBulk Density (g cm−3)Ksat Cm h−1FC (%)WP (%)AW (%)pH ECe (dS.m−1)OM (%)CaCO3 (%)
Sand %Silt %Clay %TC
0–30203842CL1.401.234.319.714.67.762.851.504.3
30–60173746CL1.360.932.219.113.17.752.981.104.2
TC = Texture class, CL = Clay loam, FC = Field capacity, WP = Wilting point, AW = Available water, OM = Organic matter, and Ksat = Hydraulic conductivity.
Table
Table 10. Physico-chemical composition of raw clover honey (on a fresh weight basis).
Table 10. Physico-chemical composition of raw clover honey (on a fresh weight basis).
Property/ComponentUnitValue
Moisture%16.8
Proteins0.28
Organic acids0.48
pH 4.14
Osmoprotectants:
Prolinemg kg−1 FW47.8
Total soluble sugars%82.6
Amino acids0.33
Sugar fractions:
Fructose%44.2
Glucose25.9
Maltose3.7
Sucrose4.21
Mineral nutrients:
Potassium (K)mg kg−1 FW456.8
Phosphorus (P)50.2
Magnesium (Mg)84.2
Calcium (Ca)71.4
Sulphur (S)77.8
Iron (Fe)69.8
Manganese (Mn)8.4
Zinc (Zn)5.5
Copper (Cu)4.6
Iodine (I)81.4
Sodium (Na)42.9
Selenium (Se)0.92
Antioxidants and Vitamins:
Ascorbic acid (vitamin C)mg kg−1 FW24.2
Thiamine (B1)0.14
Riboflavin (B2)0.18
Niacin (B3)1.67
Pantothenic acid (B5)1.08
Pyridoxine (B6)2.27
Folate (B9)0.21
DPPH radical-scavenging activity%88.2
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MDPI and ACS Style

Rady, M.M.; Boriek, S.H.K.; Abd El-Mageed, T.A.; Seif El-Yazal, M.A.; Ali, E.F.; Hassan, F.A.S.; Abdelkhalik, A. Exogenous Gibberellic Acid or Dilute Bee Honey Boosts Drought Stress Tolerance in Vicia faba by Rebalancing Osmoprotectants, Antioxidants, Nutrients, and Phytohormones. Plants 2021, 10, 748. https://doi.org/10.3390/plants10040748

AMA Style

Rady MM, Boriek SHK, Abd El-Mageed TA, Seif El-Yazal MA, Ali EF, Hassan FAS, Abdelkhalik A. Exogenous Gibberellic Acid or Dilute Bee Honey Boosts Drought Stress Tolerance in Vicia faba by Rebalancing Osmoprotectants, Antioxidants, Nutrients, and Phytohormones. Plants. 2021; 10(4):748. https://doi.org/10.3390/plants10040748

Chicago/Turabian Style

Rady, Mostafa M., Sara H. K. Boriek, Taia A. Abd El-Mageed, Mohamed A. Seif El-Yazal, Esmat F. Ali, Fahmy A. S. Hassan, and Abdelsattar Abdelkhalik. 2021. "Exogenous Gibberellic Acid or Dilute Bee Honey Boosts Drought Stress Tolerance in Vicia faba by Rebalancing Osmoprotectants, Antioxidants, Nutrients, and Phytohormones" Plants 10, no. 4: 748. https://doi.org/10.3390/plants10040748

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