1. Introduction

Legumes in different geographical regions considerably differ in their use, phyto-constituents and nutritive value. It has an important place in the traditional diets of the Mediterranean, Indian, Chinese, English, Middle Eastern, African and South American, and has considerable importance as a low-cost food rich in proteins and carbohydrates [1] . In Egypt, field bean (Vicia faba L.) is one of essential winter field crops due to its protein that is a good alternative compared with expensive meat and fish protein [2] . It is known that seed of this crop can be eaten either fresh or cooked. The most popular dishes of faba bean are Medamis “stewed beans”, Falafel “deep fried cotyledon paste with some vegetables and spices”, Bissara “cotyledon paste poured onto plates” and Nabet soup “boiled germinated beans” [3] . This protein has high nutritive value and protein contents [4] . According to FAOSTAT [5] , China, Ethiopia, France, Egypt and Australia are main faba bean producing countries. However, various processing methods such as roasting, soaking, germination or fermentation decrease the levels of anti-nutritional factors [6] . Unfortunately, faba bean production is affected by different factors such as genotypes and plant distribution, where Abd El-Rahman [7] showed that the interaction between faba bean genotypes and plant distribution had significant effect on plant height, numbers of branches and pods plant⁻¹, seed yield plant⁻¹, 100-seed weight and seed yield unit area⁻¹. Also, Safina [8] found that faba bean cultivar Giza 843 integrated positively with the widest ridge and recorded the highest seed yield ha⁻¹ compared with the other treatments.

Concerning to the advantageous belongings foliar spraying of amino acids, foliar spraying treatment of plants with naturally occurring compounds in plant cells is an easy technique and an alternative approach used to reduce mineral nitrogen (N) fertilizers uses. Improving the content of limiting amino acids by breeding seems very difficult since a strong correlation coefficient exists between protein content and the content of individual amino acids [9] . Amino acids contain both acid and basic groups and act as buffers, which help to maintain favorable pH value within the plant cell [10] and thereby impact plant growth and serve to explain how organic matter promotes soil productivity [11] . According to Rai [12] , amino acids are considered as precursors and constituents of proteins. They are participatory in the compilation of other organic compounds, such as amines, alkaloids, vitamins, enzymes and protein [13] . The valuable effects of amino acids improved growth and yield for some legume crops [14] [15] and [16] . Moreover, Zewail [17] demonstrated that foliar application with amino acids at 4 ml・L⁻¹ increased dry weight of shoots and specific growth rate of common bean plant.

A wide variety of antioxidants such as vitamins C and E, carotenoids, terpenoids and polyphenols contribute to the antioxidant capacity of plant foods [18] , where these antioxidants able to protect against reactive oxygen species, which are responsible for reactions underlying many serious diseases [19] . The differences in the phenolic composition and antioxidant activity between faba bean cultivars were observed by Chaieb et al. [20] . Also, phenolic compounds are one of the micro-constituents which have been gaining an increasing interest for their health promoting properties, largely defined by their antioxidant activity [21] , but little is known about the antioxidants present in Egyptian faba bean cultivars. Therefore, the objective of this study was to evaluate seed yield and quality of two faba bean cultivars to different rates of amino acids compounds under narrow and wide ridges.

2. Materials and Methods

A two-year study was carried out at Giza Agricultural Experiments and Research Station (Latitude 30˚00'30"N, Longitude 31˚12'43"E, 26 m.a.s.l), Faculty of Agriculture, Cairo University (Egypt), during the two successive seasons 2015/2016 and 2016/2017. This study evaluate seed yield and quality of two faba bean cultivars to different rates of amino acids compounds under narrow and wide ridges. Representative soil samples were taken from each site at the depth of 0 to 30 cm from the soil surface. The soil analysis of the experimental soil as an average of the two growing seasons 2016 and 2017, indicated that the soil is clay loam (3.95% coarse sand, 30.83% fine sand, 28.71% silt and 36.51% clay), the pH (paste extract) is 7.95, the available nutrients in mg・kg⁻¹ are N (27.45), P (12.64) and K (239). The procedure of soil analysis followed the methods of Black [22] . Furrow irrigation was the system irrigation in the region. Maize was the preceding summer crop in both seasons. The substances and the rate of spraying are illustrated in Table 1.

Calcium superphosphate (15.5% P₂O₅) was applied during soil preparation at the rate of 357 kg・ha⁻¹. Faba bean cultivars were planted in 24^th and 22^th October in 2016 and 2017 seasons, respectively. Faba bean seeds were sown in one and two rows on ridges 60 and 120 cm width, respectively. The experiment included twenty treatments which were the combinations of two ridge widths (60 and 120 cm) with two faba bean cultivars (Sakha 1 and Masr 3) with five amino acids compounds (power mix 1.5 cm・L⁻¹ “Pm₁”, power mix 3.0 cm・L⁻¹ “Pm₂”, super mix 3.5 cm・L⁻¹ “Sm₁” and super mix 7.0 cm・L⁻¹ “Sm₂”, as well as, water only “control treatment”). Faba bean cultivars were thinned to two plants spaced at 25 cm between hills.

With respect to control treatment, faba bean plants received mineral N fertilizer in form of ammonium nitrate (33.0% N) at rate of 107.1 kg N ha⁻¹ which divided to equal three doses at 20 days (before the first irrigation), 40 days (before the second irrigation) and 60 days (before the third irrigation) from planting. Also, faba bean plants of control treatment received K sulfate (48.0% K₂O) at rate of 119 kg・ha⁻¹ before the first irrigation.

With respect to four amino acids compounds treatments, faba bean plants received mineral N fertilizer in form of ammonium nitrate (33.0% N) at rate of 35.7 kg N ha⁻¹ before the first irrigation at 20 days from planting. At 40 days from planting, two treatments only received power mix at rate of 1.5 cm・L⁻¹ (Pm₁) and the other treatments received super mix at rate of 3.5 cm・L⁻¹ (Sm₁) before the second irrigation. At 60 days from planting, one of the two power mix treatments received 1.5 cm・L⁻¹ (Pm₂), meanwhile one of two super mix treatments received 3.5 cm・L⁻¹ (Sm₂) before the third irrigation.

The treatments were laid out in a split split plot distribution in randomized complete blocks design in three replications was used. Ridge width treatments were randomly assigned to the main plots, faba bean cultivars were allocated in sub plots and amino acids compounds were allocated in sub sub plots. The area of sub sub-plot was 12.0 m², each plot consisted of 5 ridges, and each ridge was 4.0 m in length and 0.6 m in width. Faba bean cultivars kindly provided by Food Legumes Research Department, ARC, Egypt.

2.1. The Studied Data

1) Photosynthesis pigments

These analyses were done in fresh leaves of faba bean shoot at 75 days from planting.

Plant pigments: Fresh leaves was extracted with dimethyl formamide and placed overnight at cool temperature (5˚C). Chlorophyll (Chl) a, b, and carotenoids were measured by spectrophotometer at wavelength 663, 647 and 470 nm, respectively. Chl and carotenoids were calculated according to the equation described by Nornai [23]

$\text{Chl}\text{a}=\text{12}.\text{7}0A_{\text{663}}-\text{2}.\text{79}{A}_{\text{647}}$ (1)

$\text{Chl}\text{b}=\text{2}0A_{\text{647}}-\text{4}.\text{62}{A}_{\text{663}}$ (2)

$\text{Carotenoids}=\frac{\left[\text{1}000\times A_{\text{47}0}-\left(\text{3}.\text{72Chl}\text{a}-\text{1}0\text{4Chl}\text{b}\right)\right]}{229}$ (3)

2) Chemical composition

These analyses were done in fresh leaves of faba bean shoot at 75 days from planting and also in faba bean seeds at harvest.

Mineral element concentration: Determinations of total N, P and K were carried out on the plant leaves were dried at 70˚C for 48 hr and the wet digestion of 0.2 g fine powder of dry material were done with sulphoric and perchloric acids as described by Piper [24] . N was determined by using the modified “Micro Kjeldahl” apparatus of Parnas and Wagner as described by Pregl [25] . P was determined spectrophotometerically by using stannous chloride method according to A.O.A.C. [26] . K was measured by flame photometer according to the method described by Brown and Lilliland [27] .

Ethanol extract: Ethanol extract of leaves was used for the determination of total sugars, and total soluble phenols and total free amino acids. For preparation of ethanol extract, 0.5 g of dry materials were adding about 25 ml of 95% ethanol for about 10 min., then filtrated through a sintered glass funnel (G3). The residue was re-extracted and filtered twice with ethanol (80%), and then the volume was adjusted to 25 ml with ethanol (80%).

Total sugars concentration: In ethanol extract, determination of total sugars concentrations were carried out by using the total sugars in was determined by phosphomolybdic acid method according to A.O.A.C. [26] .

Total soluble phenols concentration: In ethanol extract, total soluble phenols concentration was determined by using the Folin-Ciocalteu reagent according to Swain and Hillis [28] .

Total free amino acids concentration: In ethanol extract, total free amino acids concentration was determined by using ninhydrin reagent according to Moore and Stein [29] .

3) Seed yield and its attributes

At harvest, a random sample of five plants was taken from each sub sub-plot to measure the following traits: Plant height (cm), numbers of branches and pods per plant, number of seeds per pod, 100-seed weight (g) and seed yield per plant (g). Seed yield per ha (ton) was calculated from harvesting and threshing the inner three ridges of each sub sub-plot then converted to ton per ha.

2.2. Statistical Analysis

Analysis of variance of the obtained results of each season was performed. The homogeneity test was conducted of error mean squares and accordingly, the combined analysis of the two experimental seasons was also carried out. The measured variables were analyzed by ANOVA using MSTATC statistical package [30] . Mean comparisons were performed using the east significant differences (L.S.D) test with a significance level of 5% [31] .

3. Results and Discussion

A. Chemical composition and photosynthesis pigments in faba bean shoot

1) Ridge width

Significant effects of ridge width on all the studied chemical composition and photosynthesis pigments traits in faba bean shoot were observed in the combined data across the two seasons (Table 2). Faba bean plants of wide ridge had higher shoot N, P, K, total sugars, Chl a and b, as well as, total free amino acids concentrations than those of the narrow one. However, high total soluble phenols and carotenoids concentrations in faba bean shoot were observed when grown in the narrow one.

These results could be attributed to wide ridge furnished suitable basic growth resources for faba bean growth and development more than the narrow one. Particularly light is one of the most important environmental factors because it regulates photosynthetic assimilation and partitioning in plants [32] . Naturally, different tissues of faba bean leaves need different requirements of essential nutrients for satisfactory their growth.

With respect to faba plants of the narrow ridge; it is likely that intra-specific competition between them was increased for basic growth resources more than those of the other one which reflected negatively on a decrease in photosynthesis and transpiration rates. Certainly, Chl content indicates indirectly the nutritional status of plants since much of leaf N is incorporated in Chl [33] . Consequently, it is possible to suggest that total soluble phenols and carotenoids activity in faba bean shoot were due to higher concentration of the phenolic compound and total yellow pigments against assimilates translocated into different tissues of faba bean leaves than those of the wide one.

Accordingly, it is expected that that increase of the studied chemical composition (except total soluble phenols) and Chl a and b in faba bean shoot accompanied with reduced RNase and protease activity, especially polyphenols were bonded with other organic substances such as carbohydrate or protein [34] .

2) Faba bean cultivars

Faba bean cultivars were differed significantly for all the studied chemical composition and photosynthesis pigments traits in faba bean shoot except shoot Chl a and b and total free amino acids concentrations in the combined data across the two seasons (Table 2). Faba bean cultivar Sakha 1 had higher shoot N, P, K and total sugars concentrations than those of other cultivar. Meanwhile, faba

**Significance at a level of 1% of probability (p < 0.01) * Significance at a level of 5% of probability (0.01 ≤ p < 0.05) N.S. Non-Significance (p ≥ 0.05)

bean cultivar Masr 3 had higher shoot total soluble phenols and carotenoids concentrations than the other one. It seems that genetic makeup of faba bean cultivar Sakha 1 translated into suitable some morphological and anatomical characteristics which reflected positively on canopy architecture of this cultivar than the other one. These results show that plants of faba bean cultivar Sakha 1 were able to utilize the available environmental resources that reflected positively on chemical composition in their shoots more than faba bean cultivar Masr 3. It is expected that genetic makeup of faba bean cultivar Masr 3 had some biochemical aspects that restricted enzymatic oxidative cleavage which reflected on total soluble phenols and carotenoids concentrations in faba bean shoot.

3) Amino acids compounds

Amino acids compounds affected significantly all the studied chemical traits in faba bean shoot in the combined data across the two seasons (Table 2). Control and Pm₂ had higher shoot N, P, K, total sugars, Chl a and b, as well as, total free amino acids concentrations than those of the others without significant differences between them. Also, there were no significant differences between Pm₁ and Pm₂ for shoot P and total free amino acids concentrations. In other words, increasing rate of Pm from 1.5 to 3.0 cm・L⁻¹ did not increase P and total free amino acids concentrations in faba bean shoot. Moreover, there were no significant differences between Pm₁ and Sm₁ on shoot P, total sugars and total soluble phenols, Chl b, carotenoids and total free amino acids concentrations. On the other hand, there were no significant differences between Sm₁ and control treatment on shoot N and total free amino acids concentrations. Meanwhile, there were no significant differences between Sm₁ and Sm₂ on shoot Chl a and total free amino acids concentrations. In other words, increasing rate of Sm from 3.5 to 7.0 cm・L⁻¹ did not increase Chl a and total free amino acids concentrations in faba bean shoot. These results may be due the tested amino acids compounds were differed in their rates and composition (Table 1). It is likely that rate and composition of Pm₂ which included some plant growth regulators caused rapid cell division that elongated faba bean internodes [35] by promoting roots and stem length in the plant through gibberellic acid [36] , then roots grew deeper into the soil profile to extract water and soil nutrients (N, P and K) which reflected on shoot length. This biological situation could be enhanced by K citrate and micro-elements by stimulated different physiological activities.

Consequently, it is expected that foliar spraying of Pm₂ lengthened the vegetative stage and thereby there was an increase in photosynthesis pigments (Chl a and b contents) and finally more enhance in protein synthesis. According to Fletcher et al. [37] , the increase in cytokinin levels was associated with stimulated chlorophyll biosynthesis. These results are in parallel with those obtained by Ali [38] who reported that foliar application of 1% K and 1% P produced highest values of Chl a, b and a + b as compared with untreated faba bean plants. Also, El-Ghamry et al. [39] found that Chl a and b contents were increased significantly by amino acids compounds. Moreover, Abou EL-Yazied and Mady [40] indicated that foliar spraying with boron at 50 cm・L⁻¹ increased photosynthetic pigments.

On the other hand, Sm₁ had the highest shoot total soluble phenols and carotenoids concentrations compared with those of other rates. These results could be due to Sm₁ that included magnesium (Mg) activated antioxidative defense enzymes in some plant species [41] . Consequently, it is possible to suggest that this biological situation reflected positively on Mg availability in different tissues of faba bean plants that promoted plant growth and increased total soluble phenols concentration in faba bean shoot. It is known that Mg in shoots declined quickly within one day after the removal of Mg [42] suggesting that shoot and leaf are secondary response organs following changes in Mg level. It is an important to mention that decreasing rate of Sm from 7.0 to 3.5 cm・L⁻¹ could be led to negative effects on translocation rate of sucrose from leaves to phloem which reflected positively on N, P, K and total sugars concentrations in faba bean shoot.

4) Interaction between ridge width and faba bean cultivars

Data in Table 2 show interaction between ridge width and faba bean cultivars affected significantly shoot total sugars and carotenoids concentrations in the combined data across the two seasons. Growing faba bean cultivar Sakha 1 in the wide ridge had the highest shoot total sugars concentration compared with the others. These results probably due to faba bean cultivar Sakha 1 interacted positively with the wide ridge to benefit greatly from basic growth resources which reflected on concentration of shoot total sugars compared with the others. Meanwhile, growing faba bean cultivar Masr 3 in the narrow ridge had the highest shoot carotenoids concentration compared with the others. These data show that each of these two factors act dependently on total sugars and carotenoids concentrations in faba bean shoot.

5) Interaction between ridge width and amino acids compounds

Data in Table 2 show interaction between ridge width and amino acids compounds affected significantly shoot N, P and K concentrations in the combined data across the two seasons. The data indicate that faba bean plants that received Pm₂ had the highest shoot N, P and K concentrations compared with those of the other treatments. Accordingly, it is expected that cytokinines and gibberellic acid in Pm₂ had a major role in regulating ions and modifying the uptake movement and metabolism of nutrients within plant tissues of faba bean plants by increasing ridge width from 60 to 120 cm. Plants have the ability to store excessive amounts of exogenously supplied hormones in form of reversible conjugates which release active hormones when the plant needs them during the growth period [43] . These results reveal that ridge width responded differently to amino acids compounds for N, P and K concentrations in faba bean shoot.

6) Interaction between faba bean cultivars and amino acids compounds

Data in Table 2 show interaction between faba bean cultivars and amino acids compounds affected significantly Chl a and b in faba bean shoot in the combined data across the two seasons. Faba bean cultivar Sakha 1 that received Pm₂ had the highest Chl a and b in faba bean shoot compared with the others. These results show that each of these two factors act dependently on the studied Chl a and b in faba bean shoot.

7) Interaction among ridge width, faba bean cultivars and amino acids compounds

Data in Table 2 show interaction among ridge width, faba bean cultivars and amino acids compounds affected significantly photosynthesis pigments in faba bean shoot in the combined data across the two seasons. Growing faba bean cultivar Sakha 1 in the wide ridge that received Pm₂ had the highest shoot Chl a and b compared with the others. These results probably due to genetic makeup of faba bean cultivar Sakha 1 that received Pm₂ interacted positively with wide ridge to increase Chl a and b in faba bean shoot. Meanwhile, growing faba bean cultivar Masr 3 in the narrow ridge that received Sm₁ recorded the highest shoot carotenoids compared with the others. Response of plant to plant growth regulators vary with varieties, environmental conditions, physiological and nutritional status, as well as, stage of development and endogenous hormonal balance [44] . These results reveal that ridge width x faba bean cultivars x amino acids compounds had significant effects on photosynthesis pigments in faba bean shoot.

B. Seed yield and its attributes

1) Ridge width

Significant effects of ridge width on all the studied traits of seed yield and its

**Significance at a level of 1% of probability (p < 0.01) * Significance at a level of 5% of probability (0.01 ≤ p < 0.05) N.S. Non-Significance (p ≥ 0.05).

attributes except number of pods plant⁻¹ and 100-seed weight in the combined data across the two seasons (Table 3). Faba bean plants of the wide ridge had higher values of number of branches plant⁻¹, pod length, number of seeds pod⁻¹, seed yields plant⁻¹ and ha⁻¹ than those of narrow one; meanwhile plant height had opposite trend. Faba bean plants of the wide ridge increased branches number plant⁻¹ by 5.80%, pod length by 2.94%, seeds number pod⁻¹ by 3.19%, seed yield plant⁻¹ by 6.96% and seed yield ha⁻¹ by 5.27% than those of the other one. These results may be due to faba bean plants that grown in wide ridge benefited greatly from environmental basic resources that reflected positively on their efficiency in photosynthetic process more than those of narrow one.

2) Faba bean cultivars

Faba bean cultivars were differed significantly for all the studied traits in the combined data across the two seasons (Table 3). Faba bean cultivar Sakha 1 had higher plant height, numbers of branches and pods plant⁻¹, pod length, number of seeds pod⁻¹, 100-seed weight, seed yields plant⁻¹ and ha⁻¹ than those of the other cultivar. These variations between the tested two cultivars probably due to genetic makeup of each cultivar translated into suitable some morphological and physiological characteristics which responded differently to environmental conditions. Similar results were reported by Mohamed and El-Abbas [45] , Bakry et al. [46] and Safina [8] who reported there were significant differences among faba bean cultivars in seed yield and yield attributes traits.

3) Amino acids compounds

Amino acids compounds affected significantly all the studied traits in the combined data across the two seasons (Table 3). These results reveal that control and Pm₂ had higher plant height, numbers of branches and pods plant⁻¹, pod length, number of seeds pod⁻¹, 100-seed weight, seed yields plant⁻¹ and ha⁻¹ than those of the others without significant differences between them. However, there were no significant differences between Pm₁ and Pm₂ on plant height which indicating the increase in rate of Pm from 1.5 to 3.0 cm・L⁻¹ had similar effect on this trait. Also, there were no significant differences between Pm₁ and Sm₁ on plant height, numbers of branches and pods plant⁻¹, pod length, 100-seed weight, seed yields plant⁻¹ and ha⁻¹. Moreover, there were no significant differences between Sm₂ and control treatment on plant height, number of pods plant⁻¹. Furthermore, there were no significant differences between Sm₁ and Sm₂ on plant height and number of seeds pod⁻¹ which indicating the increase in rate of Sm from 3.5 to 7.0 cm・L⁻¹ had similar effect on these traits.

These results may be due to Pm₂ is compound that have high rate of amino acids, riboflavin, cytokinines, gibberellic acid, K citrate and micro-elements led to an increase in dry matter accumulation during growth and development. Particularly, boron as microelement plays a key role in higher plants by facilitating the short- and long-distance transport of sugar via the formation of borate-sugar complexes [47] . It is known that boron deficiency in crops is more widespread than the deficiency of any other micronutrients [48] . Also, zinc is a micronutrient needed in small amounts by crop plants, but its important in crop production has increased in recent years [49] . In this concern, Mady [50] showed that many growth faba bean traits as number of leaves plant⁻¹, dry weights of stems and leaves plant⁻¹, as well as, total leaf area were enhanced by foliar application of zinc. Moreover, Al-Whaibi et al. [51] found that seed yield attributes were increased by gibberellic acid application.

With respect to Sm, number of branches plant⁻¹, pod length, number of seeds pod⁻¹, seed yields plant⁻¹ and ha⁻¹ were increased by increasing rate of Sm from 3.5 to 7.0 cm・L⁻¹. These results could be attributed to increase in rate of Sm from 3.5 to 7.0 cm・L⁻¹ increased translocation rate of sucrose from leaves to phloem which reflected positively carbohydrate accumulation in the attributes of seed yield where Cakmak et al. [52] showed that Mg deficiency restricted the carbon flow to the sink organs and caused carbohydrate accumulation in the source leaves.

4) Interaction between ridge width and faba bean cultivars

Data in Table 3 show interaction between ridge width and faba bean cultivars affected significantly 100-seed weight in the combined data across the two seasons. Growing faba bean cultivar Sakha 1 in the wide ridge had the highest 100-seed weight compared to the others. It seems that faba bean cultivar Sakha 1 interacted positively with wide ridge to furnish better translocation of available assimilates from source to sink during reproductive stage of faba bean compared with the others. These results show that each of these two factors act dependently on 100-seed weight.

5) Interaction between ridge width and amino acids compounds

Data in Table 3 show interaction between ridge width and amino acids compounds affected significantly number of pods plant⁻¹ and seed yield ha⁻¹ in the combined data across the two seasons. Growing faba bean plants in the wide ridge that received Pm₂ had the highest number of pods plant⁻¹ and seed yield ha⁻¹ compared with the others. These results reveal that ridge width responded differently to amino acids compounds for number of pods plant⁻¹ and seed yield ha⁻¹.

6) Interaction between faba bean cultivars and amino acids compounds

Data in Table 3 show interaction between faba bean cultivars and amino acids compounds affected significantly number of seeds pod⁻¹ and seed yield plant⁻¹ in the combined data across the two seasons. Faba bean cultivar Sakha 1 that received Pm₂ had the highest number of seeds pod⁻¹ and seed yield plant⁻¹ compared with the others. These results show that each of these two factors act dependently on number of seeds pod⁻¹ and seed yield plant⁻¹.

7) Interaction among ridge width, faba bean cultivars and amino acids compounds

Data in Table 3 show interaction among ridge width, faba bean cultivars and amino acids compounds affected significantly number of seeds pod⁻¹ and seed yield ha⁻¹ only in the combined data across the two seasons. These results may be attributed to growing faba bean cultivar Sakha 1 in the wide ridge that received Pm₂ had the highest number of seeds pod⁻¹ and seed yield ha⁻¹ compared with the others. It seems that faba bean cultivar Sakha 1 that received Pm₂ interacted positively with the wide ridge to enhance source-sink relationship and stimulates the translocation of photoassimilates to sink thereby helping in effective flower formation and ultimately enhancing number of seeds pod⁻¹. These results reveal that each of these three factors act dependently on number of seeds pod⁻¹ and seed yield ha⁻¹.

C. Chemical composition in faba bean seeds

1) Ridge width

Significant effects of ridge width on all the studied chemical composition in faba bean seeds traits were observed in the combined data across the two seasons (Table 4). Faba bean plants of the wide ridge had higher seed N, P, K, total sugars and total free amino acids concentrations than those of the narrow one; meanwhile the reverse was true for seed total soluble phenols concentration. The wide ridge increased seed N, P, K, total sugars and total free amino acids concentrations by 10.96%, 37.44%, 9.60%, 13.71% and 32.67% than those of the narrow one. Conversely, the wide ridge decreased seed total soluble phenols concentration by 31.62% than the other one. These results may be due to faba bean plants of wide ridge decreased intra-specific competition between them for basic growth resources which activated enzyme polyphenol oxidase and led to degradation and consequent losses of total soluble phenols in faba bean seeds.

2) Faba bean cultivars

Faba bean cultivars were differed significantly for all the studied chemical composition in faba bean seeds traits in the combined data across the two seasons (Table 3). Faba bean cultivar Sakha 1 had higher seed N, P, K, total sugars and total free amino acids concentrations than those of other one; meanwhile the reverse was true for seed total soluble phenols concentration. Faba bean cultivar Sakha 1 recorded higher seed N, P, K, total sugars and total free amino acids concentrations by 11.48%, 22.81%, 14.07% and 8.44%, respectively, more than faba bean cultivar Masr 3. With respect to seed total soluble phenols concentration, the results show that total soluble phenols concentration depended on moisture content in faba bean seeds probably due to seeds of Masr 3 cultivar had lower moisture than the other one. Consequently, the observed differences in chemical composition in faba bean seeds between the two cultivars are likely to primarily reflect genotypic variation.

3) Amino acids compounds

Amino acids compounds affected significantly all the studied chemical composition in faba bean seeds traits in the combined data across the two seasons (Table 3). Control and Pm₂ had higher seed N, P, K, total sugars and total free amino acids concentrations than those of the others without significant differences between them; meanwhile the reverse was true for seed total soluble phenols concentration. However, there were no significant differences between Pm₁

**Significance at a level of 1% of probability (p < 0.01) * Significance at a level of 5% of probability (0.01 ≤ p < 0.05) N.S. Non-Significance (p ≥ 0.05).

and Pm₂ on total free amino acids meaning that this trait responded similarly to the tested rates of Pm. Meanwhile, there were no significant differences Pm₁ and Sm₂ on seed N, P, K, total sugars and total free amino acids. Moreover, there were no significant differences between Sm₂ and control treatment on total free amino acids. The results of this study suggest that Pm₂ could activate translocation of the absorbed nutrients into the seed as a result of improvements in physiological attributes in plants that received high rate of Pm. With respect to total soluble phenols concentration in faba bean seeds, Sm₁ had higher seed total soluble phenols concentration than others. It is important to mention that there were no significant differences between Sm₁ and Pm₁ for total soluble phenols concentration in faba bean seeds. It is known that tyrosinase inhibition activity is significantly correlated with total phenols and antioxidant capacity [53] . On the other hand, increasing rate of Sm from 3.5 to 7.0 cm・L⁻¹ increased seed N, P, K, total sugars and total free amino acids concentrations was due to increase in translocation rate of N, P, K and total sugars concentrations from leaves to seed during seed filling period.

4) Interaction between ridge width and faba bean cultivars

Interaction between ridge width and faba bean cultivars affected significantly N concentration in faba bean seeds in the combined data across the two seasons (Table 4). Growing faba bean cultivar Sakha 1 in the wide ridge had the highest seed N concentration compared with the others. It seems that this interaction had not significant effects on seed quality. These results reveal that each of these two factors act dependently on N concentration in faba bean seeds.

5) Interaction between ridge width and amino acids compounds

Data in Table 4 show interaction between ridge width and amino acids compounds affected significantly N, P, K, total soluble phenols and total free amino acids concentrations in faba bean seeds in the combined data across the two seasons. Growing faba bean plants in the wide ridge that received Pm₂ had the highest seed N, P, K and total free amino acids concentrations compared with the others. These results could be attributed to faba bean plants of the wide ridge that received Pm₂ furnished better growth and development conditions for faba bean plants which reflected positively on enlargement, filling and maturation of seed development compared with the others. From the other point, growing faba bean plants in the narrow ridge that received Sm₁ had the highest seed total soluble phenols concentration compared with the others. These results reveal that ridge width responded differently to amino acids compounds for N, P, K, total soluble phenols and total free amino acids concentrations in faba bean seeds.

6) Interaction between faba bean cultivars and amino acids compounds

Data in Table 4 show interaction between faba bean cultivars and amino acids compounds affected significantly N, total soluble phenols and total free amino acids concentrations in faba bean seeds in the combined data across the two seasons. Faba bean cultivar Sakha 1 that received Pm₂ had the highest N and total free amino acids concentrations in faba bean seeds compared with the others. Meanwhile, faba bean cultivar Masr 3 that received Sm₁ had the highest total soluble phenols concentration in faba bean seeds indicating good antioxidants compared with the others. The concentration and presence of these compounds in plants varied depending upon many factors, including plant genetic variation, soil composition, cultural factors and climate [54] . These results show that each of these two factors act dependently on N, total soluble phenols and total free amino acids concentrations in faba bean seeds.

7) Interaction among ridge width, faba bean cultivars and amino acids compounds

Data in Table 4 show interaction among ridge width, faba bean cultivars and amino acids compounds affected significantly N, total sugars, total soluble phenols and total free amino acids concentrations in faba bean seeds in the combined data across the two seasons. Growing faba bean cultivar Sakha 1 in the wide ridge that received Pm₂ had the highest N, total sugars and total free amino acids concentrations in faba bean seeds compared with the others. Obviously, growing faba bean cultivar Sakha 1 in the wide ridge with foliar spraying of Pm₂ achieved high quality. On the other hand, growing faba bean cultivar Masr 3 in the narrow ridge that received Sm₁ achieved good antioxidants in faba bean seeds. Although the soil nutrients are required for normal growth and development of crop, integrating both organic and inorganic chemicals for quality production should be considered [55] . These results reveal that there were significant effects of ridge width × faba bean cultivars × amino acids compounds on N, total sugars, total soluble phenols and total free amino acids concentrations in faba bean seeds.

4. Conclusion

Our results can be concluded that the limiting factor for increasing seed quality and antioxidants of the tested faba bean cultivars depends on rate and composition of amino acids. Faba bean plants of wide ridge had higher shoot and seed chemical composition except total soluble phenols than those of the narrow one. Also, Faba bean cultivar Sakha 1 gave higher N, P, K and total sugars concentrations in shoot and seeds, as well as, seed yield and its attributes than Masr 3. Moreover, faba bean plants that received Sm₁ recorded the highest antioxidants in their seeds; meanwhile faba bean plants that received Pm₂ had the highest seed quality compared with the other treatments. Growing two rows of faba bean cultivar Sakha 1 in 120 cm ridge width that received 3.0 cm・L⁻¹ of power mix increased seed yield and quality.