Alleviation of Copper-Induced Stress in Pea (Pisum sativum L.) through Foliar Application of Gibberellic Acid

Simple Summary Phytohormones are key regulators of several stages of plant growth and development as well as provide the regulatory response against various heavy metals stresses by mediating physio-morphological responses and enzymatic activities. The current study evaluated the effects of gibberellic acid (GA3) foliar applications on the performance of pea grown either in Cu-contaminated (Cu+) and non-contaminated (Cu−) soil. GA3 was applied exogenously (0, 10, 50, and 100 mg·L−1) on 15-days-old plants, and the results show that the increasing concentration of GA3 buffered the phytotoxic effects of Cu, coupled with an increase in plant growth and physiological variables. The results also showed that foliar-applied GA3 up to 100 mg·L−1 alleviated the oxidative stress, as inferred from the lower concentrations of malondialdehyde (MDA) and H2O2, which mirrored the increased activity of antioxidant enzymes, i.e., superoxide dismutase, peroxidase, and catalase. In addition, enhanced growth, physiology, and enzymatic activities were also observed in pea plants sprayed with GA3 up to 100 mg·L−1 in Cu− soil. Overall, the foliar application of GA3 boosted phytoextraction of Cu from the soil and alleviated the oxidative stress in pea plants grown in Cu-polluted soil. Abstract Copper (Cu) is an essential metal for plants. However, its excess in soil can adversely affect plant metabolism. The current study evaluated the effects of gibberellic acid (GA3) foliar applications on the performance of pea plants grown either in Cu-contaminated (Cu+) and non-contaminated (Cu−) soil. GA3 was sprayed (0, 10, 50, and 100 mg·L−1) on 15-days-old plants. The results showed that the increasing concentration of GA3 buffered the phytotoxic effects of Cu and enhanced plant growth, photosynthesis, and leaf chlorophyll content. Foliar-sprayed GA3 up to 100 mg·L−1 alleviated the oxidative stress, as inferred from the lower concentrations of MDA and H2O2 (33.3 µmol·g−1 and 182 µmol·g−1, respectively), and boosted the activity of superoxide dismutase (64.4 U·g−1·FW), peroxidase (122.7 U·g−1·FW), and catalase (226.3 U·g−1·FW). Interestingly, GA3 promoted Cu accumulation in different plant parts when compared to untreated plants, likely due to increased photosynthetic and transpiration rates. Overall, foliar application of GA3 promoted phytoextraction of Cu and alleviated the oxidative stress in pea plants grown in Cu+ soil.


Introduction
Pea (Pisum sativum L.) is an important leguminous crop, whose high protein content (up to 22-23%) is almost three times that of cereals [1]. The crop is mainly cultivated in tropical and sub-tropical regions of the world, and has the ability of nitrogen (N) fixation in soil through N fixing bacteria residing in roots. It has a deep root system, and hence is highly drought tolerant [2]. It has good nutritive value, as it contains considerable amounts of lysine, thiamine, riboflavin, iron, and niacin, and its product is represented by green pods or mature seeds as meal worldwide [2]. In pea, physio-morphological and biochemical events are the most crucial on which the whole productivity relies, and both are influenced by metals toxicity [3]. Heavy metals contamination is becoming increasingly common in many agricultural farmlands worldwide, due to long-term mining activities which endanger crops yield and food security [4,5]. This feature is of major concern in agricultural systems, due to the adverse effects on crop growth and physiology (phytotoxicity), food safety and marketability, soil micro biota, and most importantly on human health [6]. In addition, the dynamic equilibrium between production and elimination of reactive oxygen species (ROS) under normal growth conditions can be altered due to toxic levels of heavy metal, which results in disruption of structure and functioning of cell membranes as a result of lipid peroxidation, malondialdehyde (MDA), and hydrogen peroxide (H 2 O 2 ) accumulation [7]. Nevertheless, remediation of metal-contaminated soils by conventional (physical and chemical) methods is not ideal, as it requires huge resources, is time consuming, and sometimes even environmentally hazardous [8]. However, more recent emerging technologies, such as exogenous application of phyto-hormones, due to their ease, efficiency, and environmentally friendliness for phytoremediation should be considered for remediation [4].
Gibberellic acid (GA 3 ) is a plant hormone involved in several stages such as cell division, plant height, tissue differentiation, dry matter accumulation, net assimilation rate, leaf expansion, elongation, flowering, photosynthesis, and transpiration rate [9][10][11]. In addition, GA 3 is a kind of diterpenoid compound, and is known to play key roles to enhance phytoremediation efficiency of many crops by mediating physiology, morphology, and enzymatic activities [12,13]. Previous literature reported that exogenous supplementation of GA 3 as foliar spray significantly enhanced growth and phytoextraction efficiency of different crop plants such as Zea mays L., Tagetes patula L., Solanum nigrum L., and Corchorus capsularis L. grown on Cu, cadmium (Cd), lead (Pb), and benzo[a]pyrene-contaminated soil [4,[13][14][15].
Exogenous applications of GA 3 have a remarkable role in S. nigrum for substantial increases in growth and development [13]. In addition, a considerable increase in growth and biomass accumulation of Carapichea ipecauanha was observed in plants that received foliar applied GA 3 as compared to untreated plants [16]. Previous literature also reported the protective role of GA 3 with improved photosynthetic performances in chromium (Cr)contaminated soil [10]. The possible reason behind this mechanism might be the enhanced antioxidant activities that reduced the oxidative damage of Corchorus capsularis L. plants growing in Cu-contaminated soil [4]. There is a lot of literature on exogenous supplementation of GA 3 to enhance plant growth and development in metal-contaminated soil, however, available on other plant species, such as and Solanum nigrum L., and Tagetes patula L. [12,15]. The uniqueness of Pisum sativum L. plants due to high nutritive value and negative impacts of Cu on human health demands phytoremediation; however, sufficient information is not available regarding Cu tolerance, antioxidative defense mechanism, and Cu accumulation in different parts of this species, when grown under different concentrations of foliar applied GA 3 . Therefore, it is vital to explore the protective and growth promoting role of GA 3 in Cu-contaminated soils. It may be hypothesized that GA 3 alleviates Cu and oxidative stresses by modulating some physio-morphological and biochemical processes in pea. To test this hypothesis, pea plants were germinated on Cu-contaminated soil and then foliar sprayed with 10, 50, and 100 mg·L −1 GA 3 at 15 days after germination. In addition to evaluating key stress benchmarks on plant growth (plant height, plant weight, leaf chlorophyll, photosynthesis, and transpiration rates), accumulation of electrolytes, H 2 O 2 and MDA, and activities of key of radical oxygen-scavenging enzymes catalase, peroxidase, and superoxide dismutase were also quantified.

Experimental Site and Growth Conditions
The soil for the pot experiment was collected from the Research Area, Department of Agronomy, University of Agriculture, Faisalabad City, Punjab Province, Pakistan (30.37 • N, 69.34 • E) at depth of 0-20 cm. After grinding, the soil was mixed thoroughly, air dried under shade, and sieved through a 5 mm sieve before filling in pots (10 kg soil per pot). The textural class of soil for experimentation was loam and, before the start of the experiment, had the following characteristics: Electrical conductivity (EC) 0.432 dSm −1 , pH 7.5, available K 344 mg·kg −1 , available P 12.21 mg·kg −1 , and Cu 109 mg·kg −1 . Total Cu (2000 mg·kg −1 ), as CuSO 4 ·5H 2 O, was mixed thoroughly in soil prior to filling in pots, to simulate Cu contamination (Cu+ soil) [4]. The same number of experimental units without Cu addition in the soil were included as control (Cu− soil). A pea variety with indeterminate growth habit, "Sarsabz" (Pisum sativum L.) with 98% germination capacity was procured from Ayub Agricultural Research Institute, Faisalabad, Pakistan and used throughout the course of the experiment. The experiment was conducted in the glasshouse at the Research Area, Department of Agronomy, University of Agriculture, Faisalabad, from November 2018 to January 2019. Plants in the glasshouse received natural light, with day/night average temperature of 26/15 • C and day/night average humidity of 65/80%. The bi-factorial experiment was laid out under completely randomized design (CRD), with four replications (each replication contained five pots for each treatment). Ten seeds were directly sown in each pot. Each replication contained 50 plants of each experimental unit. Irrigation, weeding, and necessary agronomic practices, based on physical observations, were done when needed.

Exogenous Application of GA 3
Foliar sprays of GA 3 were done 14 days after seeding. From 10:00 until 11:00 am, treatments, i.e., 0, 10, 50, 100 mg·L −1 were applied by exogenously spraying GA 3 on whole seedlings until solution falls and treatments were applied only once during the whole experiment [4].

Plant Growth Attributes
Five uniform plants were randomly selected from each replication to determine the number of leaves, plant height, and plant relative fresh and dry weights at 40 days after seeding (DAS). To determine relative fresh and dry weights, plants were washed with distilled water, dried with paper and weighed for their fresh weight followed by oven drying at 70 • C until constant weight achieved. After oven drying, dry weights were recorded.

Physiological Variables
At 40 DAS from five uniform randomly selected plants from each replication, leaf chlorophyll content was measured with a chlorophyll SPAD meter (CCM-200 plus, Opti-Sciences, Hudson, NH, USA) according to manufacturer's instructions, and presented as SPAD values. On the same date measurements of net photosynthetic rate (µmol CO 2 m −2 ·s −1 ), stomatal transpiration rate (mmol H 2 O m −2 ·s −1 ), and CO 2 concentration (µmol·mol −1 ) were made on fully expanded leaves from the top of the plant canopy by using an open system LCA-4 (ADC BioScientific Ltd., Hoddesdon, UK). These measurements were made from 10:00 to 11.00 a.m., with the following specifications: Ambient pressure (P) 88.76 kPa, molar flow of air per unit leaf area (Us) 201.89 mol m −2 ·S −1 , temperature of leaf chamber (Tch) varied from 38.9 to 42.4 • C, leaf chamber molar gas flow rate (U) 236 µmol·S −1 , leaf surface area 10.11 cm 2 , and photosynthetically active radiation (PAR) at leaf surface was maximum up to 887 µmol m −2 ·s −1 .

Oxidative Stress Indicators and Antioxidant Response
To determine malondialdehyde (MDA) content, an indicator of lipid peroxidation, 0.1 g leaves were ground with 25 mL of 50 mM phosphate buffer solution containing 1% polyethylene pyrrole with the help of pestle and mortar. After centrifugation at 12,000× g for 15 min at 4 • C, the supernatant was taken, followed by heating at 100 • C for 20 min. The tubes were quickly cooled in an ice bath after heating. The absorbance was taken at wavelengths of 532, 600, and 450 nm by using a spectrophotometer (T60 U Spectrophotometer, PG Instruments Ltd., Leicestershire, UK) [17].
To determine H 2 O 2 concentration, leaf samples (1 g) were ground in 9 mL of normal saline solution (4.5 g NaCl added in 500 mL ddH2O) followed by centrifugation at 10,000× g for 10 min. Three tube types were prepared, namely empty, standard, and sample tubes. Briefly, reagent 1 and 2 (1.0 mL) in all tubes, H 2 O (0.1 mL) in empty tube, standard solution (0.1 mL) in standard tube, and sample (0.1 mL) in sample tube was added. The absorbance was taken at 405 nm with spectrophotometer according to H 2 O 2 determination kit (Nanjing Jiancheng Biology Co., Ltd., Nanjing, China).
To determine electrolyte leakage (EL), fully expanded leaves from the top of the plant canopy were taken, followed by cutting into minor slices (5-6 mm length), placed in sterilized test tubes having 8 mL distilled water, incubated, and transferred to water bath for 12 h prior to measuring the initial electrical conductivity (EC 1 ). After measuring the initial EC 1 , samples were autoclaved at 121 • C for 20 min followed by cooling down to 25 • C to measure the final electrical conductivity (EC 2 ). To measure the electrolyte leakage, a pH/conductivity meter (INCO-LAB Company, Al Kuwayt, Kuwait) was used, then the following equation for EL calculation was applied: To determine antioxidant activities, 0.5 g leaves were ground using a tissue grinder in 8 mL of cooled phosphate buffer (pH 7.0, containing 1% (w/v) polyvinylpyrolidone) in test tubes. The homogenate was centrifuged at 15,000 rpm for 20 min at 4 • C. The supernatant was used for assays of enzymes activity. The activity of catalase (CAT) and peroxidase (POD) was measured by using the method of Maehly [18]. The reaction solution (3 mL) contained 0.1 mL standard enzyme extract, 15 mM H 2 O 2, and 50 mM phosphate buffer (pH 7.0). The absorbance was taken at 240 nm with the spectrophotometer. The POD reaction solution (3 mL) contained 0.1 mL enzyme extract, 50 mM sodium acetate buffer (pH 5.0), 40 mM H 2 O 2 , and 20 mM guaiacol. The absorbance was taken at 470 nm. The superoxide dismutase (SOD) reaction solution (3 mL) contained 1.3 µM riboflavin, 50 µL enzyme extract, 50 µM nitroblue tetrazolium (NBT dissolved in ethanol), 13 mM methionine, 50 mM phosphate buffer (pH 7.8), and 75 nM EDTA [19]. The absorbance was taken at 240 nm.

Copper Concentration in Roots, Leaves and Stems
To determine the Cu content, in root, leaves, and stems, respective parts from ten uniform randomly selected plants were taken, oven dried, and ground at 40 DAS. Briefly, 0.1 g of the respective ground sample was digested in HNO 3 /HClO4 (4:1) solution followed by dilution of digested sample in de-ionized water up to final volume of 25 ml. The supernatant was taken and passed through a filter paper. Copper standard solution (SRM-3114, 10% HNO 3 , Sigma-Aldrich, Milwaukee, WI, USA) was used as a primary calibration standard for the quantitative determination of copper in roots, leaves, and stem of pea. Readings were taken by using a Perkin-Elmer 3100 Atomic Absorption Spectrophotometer (Thermo Fisher Scientific, Lancashire, UK).

Statistical Analysis
A two-way analysis of variance (Cu contamination of soil × GA 3 application) was executed to evaluate the effects of GA 3 on the recorded variables both under normal Biology 2021, 10, 120 5 of 14 (without Cu stress, control) and under Cu-contaminated soil conditions. Tukey's honestly significance difference (HSD) test was used for comparison of treatment means (p ≤ 0.05), using a statistical software package 'Statistix 8.1' (https://www.statistix.com/). A principal component analysis among treatments and dependent variable was executed using XLSTAT ver. 2018 (https://www.xlstat.com/) to delineate the effect of different doses of GA 3 on physiological growth attributes of pea plants grown in Cu− and Cu+ soil. Clustering of observations and variables into groups were done on the basis of their highest squared cosine values corresponding to factors, F1 and F2. Correlation coefficients among variables were determined with Pearson (n) method.

Plant Growth Attributes
The results revealed that the untreated plants grown in Cu+ soil exhibited the minimum plant height (19.33 cm) as compared to the other treatments. Though all foliar applied GA 3 concentrations enhanced the plant height of pea, however, the plants treated with 100 mg·L −1 GA 3 showed the maximum height in both soils (40.1 cm in Cu− soil; 34.2 cm in Cu+ soil). Similarly, maximum plant relative fresh weight (34 g) was recorded in plants receiving 100 mg·L −1 GA 3 grown in Cu− soil followed by the plants receiving same treatment grown in Cu+ soil, indicating that GA 3 increased the above ground biomass accumulation in pea (Table 1). In the case of plant dry weight, the plants treated with 100 mg·L −1 GA 3 showed the highest values in both soils (17.2 g Cu− soil and 15.2 g Cu+ soil) followed by 50 and 10 mg·L −1 GA 3 (Table 1). Similar to the aforesaid variables, plants treated with GA 3 showed an increased number of leaves in a dose-dependent manner as compared to control. The plants treated with 100 mg·L −1 showed the maximum number of leaves in both soils (30.1 Cu− soil and 28.3 Cu+ soil). The lowest values for plant height, fresh/dry weight, and number of leaves per plant were recorded in control followed by 10 mg·L −1 GA 3 application in both Cu− and Cu+ soil (Table 1).

Oxidative Stress Indicators and Antioxidant Response
Plants grown in Cu− soil, when treated with 100 mg·L −1 GA3, showed minimum MDA and H2O2 contents and electrolyte leakage (23 µ mol·g −1 , 143.32 µ mol·g −1 , and 27.2%, respectively). The plants grown in Cu+ soil exhibited increased electrolyte leakage, MDA, and H2O2 contents than those were grown in Cu− soil. The exogenous application of GA3 significantly reduced electrolyte leakage, MDA, and H2O2 contents in a concentration-dependent manner. The maximum decrease in MDA, H2O2, and electrolyte leakage were observed in plants treated with 100 mg·L -1 GA3 in Cu− (63.29%, 63.40%, and 62.84%, respectively) and Cu+ soils (54.12%, 58.79%, and 57.66%, respectively) as compared to other experimental units and control (Figure 2).  The exogenous application of 100 mg·L −1 GA3 exhibited maximum SOD activity in the plants grown in Cu− soil (75 U·g −1 ·FW) followed by the plants grown in Cu+ soil (64.39 U·g −1 ·FW). In similarity with the aforementioned variable, the highest POD activity (136.21 U·g −1 ·FW) was also observed in pea plants grown in Cu− soil treated with 100 mg·L −1 GA3. Plants receiving foliar application of 50 mg·L −1 GA3 also showed better performance in both soil conditions. In the case of CAT activity, maximum value (245 U·g −1 ·FW) was also recorded in plants treated with 100 mg·L −1 GA3 in Cu− soil. The reduced activity of antioxidants i.e., SOD, POD, and CAT in untreated plants grown in Cu+ soil indicates a significant effect of Cu stress on pea plants (Figure 3). The exogenous application of 100 mg·L −1 GA 3 exhibited maximum SOD activity in the plants grown in Cu− soil (75 U·g −1 ·FW) followed by the plants grown in Cu+ soil (64.39 U·g −1 ·FW). In similarity with the aforementioned variable, the highest POD activity (136.21 U·g −1 ·FW) was also observed in pea plants grown in Cu− soil treated with 100 mg·L −1 GA 3 . Plants receiving foliar application of 50 mg·L −1 GA 3 also showed better performance in both soil conditions. In the case of CAT activity, maximum value (245 U·g −1 ·FW) was also recorded in plants treated with 100 mg·L −1 GA 3 in Cu− soil. The reduced activity of antioxidants i.e., SOD, POD, and CAT in untreated plants grown in Cu+ soil indicates a significant effect of Cu stress on pea plants (Figure 3). Biology 2021, 10, x 8 of 14

Cu Concentration in Roots, Leaves and Stem
The GA3-untreated plants grown in Cu-soil exhibited minimum Cu concentration in roots, leaves, and stem of pea plants (16.

Cu Concentration in Roots, Leaves and Stem
The

Multivariate Analysis
Factor F1, having eigenvalue 13.711 and variability of 80.65% showed positive correlation among plant height, biomass accumulation, photosynthetic rate, transpiration rate, CO 2 index, H 2 O 2 contents, SOD, POD, and CAT activity with 50 and 100 mg·L −1 GA 3 treatment in plant grown in Cu− soil, as well as 100 mg·L −1 GA 3 treatment in plant grown in Cu+ soil. Malondialdehyde, electrolyte leakage, and H 2 O 2 contents are shown in the negative side of the F1 axis, indicating their negative correlation with 100 mg·L −1 GA 3 and positive correlation with control (no GA 3 treatment) ( Table 3) (Figure 4). Second factor F2, having eigenvalue 3.059 and variability of 17.99% represented Cu contents in leaves, roots, and stems. Cu contents in leaves, roots, and stem are shown in the positive half of F2 depict their positive correlation with 50 mg·L −1 GA 3 treatment on plants grown in Cu+ soil, while negative correlation with 10 mg·L −1 GA 3 treatment on plants grown in Cu− soil. Thus, principal component analysis delineated the morphologi-cal, physiological, and oxidative response of pea plants under the influence of GA 3 and Cu toxicity.

Multivariate Analysis
Factor F1, having eigenvalue 13.711 and variability of 80.65% showed positive correlation among plant height, biomass accumulation, photosynthetic rate, transpiration rate, CO2 index, H2O2 contents, SOD, POD, and CAT activity with 50 and 100 mg·L −1 GA3 treatment in plant grown in Cu− soil, as well as 100 mg·L −1 GA3 treatment in plant grown in Cu+ soil. Malondialdehyde, electrolyte leakage, and H2O2 contents are shown in the negative side of the F1 axis, indicating their negative correlation with 100 mg·L −1 GA3 and positive correlation with control (no GA3 treatment) ( Table 3) (Figure 4).

Discussion
Several studies have shown that Cu toxicity severely influences growth and productivity of leguminous crops [20][21][22]. In the present study, the pea plants grown in Cu+ soil showed reduced growth and biomass accumulation as compared to the plants grown in Cu− soil (Table 1). Our results are consistent with those of Massoud et al. [23], who reported that the Cu toxicity reduced the fresh biomass of pea plants. The exogenous application of phytohormones is considered a way to mitigate the toxic effects of heavy metals and increase plant tolerance to some abiotic stressors [24]. In our experiment, the foliar applied GA 3 alleviated the toxic effect of Cu and enhanced plant height, number of leaves, and biomass accumulation in pea plants grown in both Cu+ and Cu− soil (Table 1). These findings are in line with other studies that reported the remarkable role of exogenous application of GA 3 to enhance plant growth and tolerance to heavy metals such as Cd [25][26][27]. In accordance with our study, the exogenous application of 100 mg·L −1 GA 3 enhanced shoot fresh and dry weight of jute under Cu stress [4]. In the present study, enhanced plant growth variables with the exogenous application of GA 3 in Cu-stressed plants might be due to better gaseous exchange attributes [4], or GA3 helps in decreasing free metal ions in plants as suggested by Shafigh et al. [28].
Gibberellins stimulate plant growth and alleviate the inhibitory effects of different abiotic stressors on plant physiological and growth attributes, such as plant biomass accumulation, chlorophyll, minerals accumulation, gas exchange, electrolyte leakage, as well as the activity of reactive oxygen species [29][30][31]. According to Lüttge [32], photosynthetic efficiency of plants depends on chlorophyll content, which plays a key role in light dependent reaction of photosynthesis. Previous literature also stated that increased production of antioxidants in chloroplast resulted in scavenging of ROS and curtail oxidative damage to photosynthetic membranes [4]. Our findings revealed that chlorophyll content and gas exchanges were significantly influenced by the exogenous application of GA 3 (Figure 1). Though all GA 3 concentrations applied improved the physiological attributes in both Cu+ and Cu− soil, higher values were observed in experimental units received 100 mg·L −1 GA 3 . The chlorophyll content and gaseous exchange attributes were reduced in Cu+ soil as compared to Cu− soil (Figure 1). The reason behind this phenomenon might be the structural damage of chloroplast resulted from Cu exposure in the soil system [33]. Structural damage to chloroplast imparted negative influence on the photosynthetic efficiency due to damaged thylakoids which resulted in lower chlorophyll contents [34]. Nevertheless, exogenous application of GA 3 as foliar spray significantly buffered these negative effects in Cu-stressed plants. Previous literature also stated the protective role GA 3 toward the photosynthetic machinery in metal contaminated soil [10]. The possible reason behind this mechanism might be the enhanced antioxidant activities that reduced the Cu-induced oxidative damages [35]. The decreased photosynthetic performances of plants without GA 3 application may be linked to Cu toxicity and findings support the observation of Habiba et al. [36] who claimed that Cu toxicity caused a decline in chlorophyll biosynthesis and increased damage of thylakoid membranes.
Copper stress rigorously impeded the performance of crop plants [37]. In addition, Cu stress promoted oxidative damage as inferred from the enhanced production of ROS. Increased synthesis of ROS and accumulation in plant tissues cause damage to cellular structures and macromolecules such as nucleic acid, proteins, lipids, and the photosynthetic apparatus [38]. However, it has been reported that increased synthesis of antioxidant enzymes such as SOD, POD, and CAT improved the response of Oryza sativa [39] and Brassica napus [40] plants under Cu stress. Accordingly, in the present study, the alleviation of oxidative stress resulted from enhanced antioxidant activities. The findings of our study also highlight the effectiveness of foliar applied GA 3 in both Cu+ and Cu− soils. Foliar application of GA 3 (100 mg·L −1 ) decreased the production of MDA, H 2 O 2 contents, and electrolyte leakage compared to control (no GA 3 application). In contrast, all concentrations of foliar applied GA 3 enhanced the activities of SOD, POD, and CAT, but higher values for antioxidants enzymes were linked with 100 mg·L −1 GA 3 (Figures 2 and 3). The enhanced antioxidants activity can be considered as an indication of decreased accumulation of MDA and H 2 O 2 contents [4,33,41]. These findings are supported by the results of Saleem et al. [4] who reported a similar effect of foliar applied GA 3 to ameliorate the oxidative stress response in Corchorus capsularis L. Moreover, upregulation of activity of various antioxidant enzymes such as SOD, POD, and CAT shows the higher capacity of plants to scavenge excessive ROS under Cu stress [4]. The results of the current study are also in line with Fahad et al. [42], who argued that when the scavenging system against ROS is not effective, then crop plants become vulnerable to oxidative damages.
Depending on growth conditions, plants vary in their capacity of Cu uptake and accumulation. Plant roots play a central role in Cu uptake and transfer to stem and leaves through the xylem [43,44]. Pea plants treated with GA 3 exhibited enhanced Cu accumulation in roots, leaves, and stem under Cu stress ( Table 2). The increased gaseous exchange attributes such as photosynthesis and transpiration rate as the result of exogenous application of GA 3 was likely the reason behind the increased Cu uptake by plants, even under phytotoxicity conditions [4,36]. The efficacy of GA 3 to modulate the plant physiological status depends on its concentration, application method, and plant genetics [4]. The results of the present study also showed that the response of pea plants growth and development to GA 3 application changed with change in concentration, mostly under Cu stressing conditions, overall, suggesting that GA 3 promoted growth of pea plants and alleviated the Cu toxicity. To this end, foliar application of 100 mg·L −1 induced the best response in pea plants in terms morphological, physiological, and oxidative attributes.

Conclusions
Gibberellic acid is a key regulator of several stages of plant growth, development, physiology, and morphology in plants, showing also pivotal regulatory effects against various environmental stressors. In this study, foliar application with different concentrations of GA 3 proved to be successful for enhancing tolerance to Cu stress in pea plants, as evidenced from higher plant growth and antioxidant activity. In this view, the foliar application of a 100 mg·L −1 GA 3 solution proved to be the most effective in enhancing tolerance to Cu and related oxidative stresses in pea plants, while at the same time maximizing the Cu content in plant organs. Results also reveal that GA3 alleviated Cu-induced stress on pea plants by stimulated activities of reactive oxygen-scavenging enzymes catalase, peroxidase, and superoxide dismutase, which not only helped in reducing electrolyte leakage, but also hindered accumulation of MDA and H 2 O 2 in Cu-stressed pea plants. Overall