Skip to main content
PLOS One logoLink to PLOS One
. 2021 May 28;16(5):e0252396. doi: 10.1371/journal.pone.0252396

Nitrogen and boron nutrition in grafted watermelon I: Impact on pomological attributes, yield and fruit quality

Kemal Yalçın Gülüt 1,*
Editor: Shahid Farooq2
PMCID: PMC8162669  PMID: 34048470

Abstract

Watermelon is extensively consumed fruit across the globe. However, limited is known about interactive effect of nitrogen (N) and boron (B) nutrition on pomological, yield and fruit quality attributes of grafted watermelon. This two-year study tested the influence of different N and B doses on pomological, yield and fruit quality attributes of grafted watermelon under field conditions in Çukurova plains of Turkey. Four different N (0, 90, 180 and 270 kg ha-1) and two B doses (0 and 2 kg ha-1 B) were tested. The individual and interactive effects of N and B significantly altered pomological, yield and fruit quality attributes during both years. Overall, application of 270 kg ha-1 N and 2 kg ha-1 B improved yield, pomological and fruit quality attributes during both years. The highest values for yield, main stem length, stem diameter, fruit weight, fruit width, number nodes and branches per stem were recorded for 270 kg ha-1 N during both years. However, rind thickness was not altered by N application. Similarly, the highest values for quality attributes such as sucrose, glucose, fructose, citric acid, tartaric acid and ascorbic acid were noted for 270 kg ha-1 N during both years. Interestingly, no N application and 90 kg ha-1 N recorded the highest values of maleic acid during both years. The highest values of rind thickness, fruit length, fruit width and fruit weight were noted for 2 kg ha-1 B during both years, while B application had no effect on main stem length, main stem diameter, number of nodes and number of branches. Regarding N by B interactions, 180 and 270 kg ha-1 N with both B doses observed the highest values for yield, pomological and quality attributes during each year. These results indicate that N has significant contribution towards yield, pomological attributes and fruit quality of grafted watermelon. Therefore, N should be applied at the rate of 270 kg ha-1 for better yield, pomological attributes and fruit quality. Nonetheless, where necessary grafted watermelon should be fertilized with 2 kg ha-1 B for better fruit quality and pomological attributes.

Introduction

Nutrients are the most important component of growing environment for plants and influence their growth and yield. Yield and quality of field crops is positively influenced by major macro nutrients, i.e., nitrogen (N) [1, 2] or N-phosphorus-potassium [3, 4]. Moreover, N affects several traits influencing biomass production [2]. Nitrogen increases the number and size of leaf cells [3, 5]. Moreover, N-availability influences secondary metabolites, plant growth and differentiation processes [6, 7]. However, excessive use of N has been questioned recently due to huge leaching/volatilization losses and adverse effects on the environment.

Nitrogen is regarded as the growth-limiting nutrient due to its role in plant growth and productivity [8]. It is an integral part of numerous biomolecules, including enzymes, structural proteins, chlorophyll, adenosine triphosphate (ATP) and nucleic acids (DNA and RNA). Dry biomass production, leaf area and photosynthetic capacity are directly affected by N. Optimum N supply is mandatory for healthy plant growth and higher crop yield [9]. Thus, majority of crop varieties are selected and developed under optimum N fertilization.

Reproductive and vegetative growth phases, leaf emergence rate, grain yield and yield components are significantly reduced by N-deficiency [10]. Nonetheless, applied N is not used efficiently. For instance, <40% of applied N is taken up and utilized by barley [11]. Hence, farmers are concerned to increase N-use efficiency (NUE) to obtain higher crop yields. The application of N fertilizer has increased by >8-folds since 1961 [12]. This implies that excessive N application and low NUE could have adverse effects, including soil acidification, agriculture-related pollutions, and negative impacts on soil microbial activity [13, 14]. The harmful effects of N losses from the soil have toxicological implications for ecosystems and living organisms [1517].

Micronutrients are essential in appropriate concentration for plant growth and development. These nutrients play a significant role in most of the physiological processes like photosynthesis, respiration and various enzymatic reactions. Their deficiency or excess disturbs metabolic activities occurring during different plant development stages. Both deficiency and excess can cause chlorosis, necrosis, stunted growth and mottled leaves etc.

Boron (B) has narrow toxicity and deficiency range. The prime function of B is linked to the formation of cell wall and cell membranes, pollination, pollen germination, cell division, translocation of carbohydrates and metabolism of calcium, indole acetic acid and RNA [18]. Boron is many times concomitant with N, phosphorous, potassium and calcium in plants; hence, required for high yield of crops.

Boron is involved in cell wall structural integration and regulates porosity and tensile strength of the cell wall [19]. The plants require higher B than other trace/micronutrients [20]. However, the excess and deficiency of B negatively affects plant growth [2124]. Boron is found in the soil within 10–300 mg kg−1 range [25].

Watermelon (Citrullus lanatus L.) is globally important commercial vegetable fruit. China leads watermelon production of the globe, whereas Turkey follows China in terms of production [26]. Turkey has 10% share in global watermelon production. The production is negatively affected by several factors, including plant nutrients [26, 27]. Nitrogen and B are critical nutrients required for optimum production of watermelon [2630]. However, limited is known about the interactive effect of N and B on yield, pomological attributes and fruit quality of grafted watermelon in Turkey.

Therefore, this study assessed the impact of different N and B doses on yield, pomological and fruit quality attributes. It was hypothesized that increasing N and B doses would improve yield, pomological and fruit quality attributes.

Materials and methods

Studied species and experimental site

Watermelon is considered as a xerophytic tropical fruit. Its cultivation is spread over warm regions [31]. The current study was conducted at experimental fields of Research and Application Center, Çukurova University, Faculty of Agriculture, Department of Soil Science and Plant Nutrition, Turkey during watermelon growing seasons of 2018 and 2019. Grafted watermelon cultivar ‘Starburst’ was used as experimental material. The experiment was laid according to split-plot design with N as main factor and B as sub-factor. All experimental treatments had four replications.

Seedlings were planted keeping 4 m distance between rows, 1.2 m between plants and 6 plants were grown in each replication. The soil was analyzed prior to the initiation of experiments and depending on the results of the soil analysis 25 kg of phosphorus (P2O5) was applied per hectare at the time of planting.

Four different N doses, i.e., N0 (0 kg N ha-1), N1 (90 kg N ha-1), N2 (180 kg N ha-1) and N3 (270 kg N ha-1) and two different B doses, i.e., B0 (0 kg ha-1 B) and B2 (2 kg ha-1 B) were used in the study. Nitrogen was supplied by using urea and applied in three equal splits (i.e., at sowing, flowering and fruiting). Etidot67-B was used as B source and whole amount of B was applied at the time of sowing.

When plants were 45 days old, pomological characteristics such as main stem length (cm), number of branches (pieces), main stem diameter (mm) were measured with the help of meters and calipers in the field. Depending on the climatic conditions (the first week of July), the harvesting process was carried out by hand picking the fruits by drying the auricles and leeches on the fruit stalk. The yield was computed based on the weight of harvested fruits. The pomological features were realized by taking 3 fruits from each parcel.

Statistical analysis

The collected data for nutrient uptake were tested for normality by Shapiro-Wilk normality test [32]. The data were normally distributed; therefore, original data were used in statistical analysis. The differences among the years were analyzed by paired t test, which were significant. Therefore, data of both years were analyzed and presented, separately. Two-way analysis of variance (ANOVA) was used to test the significant differences among N and B doses, and their interaction [33]. Least significant difference at 5% probability was used to separate the means where ANOVA indicated significant differences.

Results

Growth and yield attributes

The individual and interactive effect of N and B significantly altered various growth and yield attributes with some exceptions during both years (Table 1). Nitrogen doses significantly altered all growth attributes except number of branches during both years. However, the growth attributes were not altered by B doses during both years, except for the only significant effect on number of branches during 2nd year. Regarding N by B interactions, all growth attributes were significantly affected except for the non-significant effect on number of branches during 1st year (Table 1).

Table 1. Analysis of variance for different pomological traits of grafted watermelon grown under varying nitrogen and boron levels.

2018 2019
Rind thickness
Source DF SS MS F value P value SS MS F value P value
Nitrogen (N) 3 3.49 1.16 0.38 0.767 4.18 1.39 0.54 0.6582
Boron (B) 1 24.73 24.73 8.07 0.005 10.56 10.56 4.07 0.0466
N × B 3 66.21 22.07 7.20 0.000 19.77 6.59 2.54 0.0615
Fruit length
Nitrogen (N) 3 4568.49 1522.83 5.65 0.001 7298.79 2432.93 7.05 0.0003
Boron (B) 1 11969.45 11969.45 44.44 0.0001 0.09 0.09 0.00 0.9872
N × B 3 678.53 226.18 0.84 0.476 440.52 146.84 0.43 0.7351
Fruit width
Nitrogen (N) 3 2649.68 883.23 7.97 0.0001 5077.99 1692.66 13.51 0.0001
Boron (B) 1 5527.97 5527.97 49.91 0.0001 816.86 816.86 6.52 0.0124
N × B 3 821.94 273.98 2.47 0.069 305.32 101.77 0.81 0.4906
Dry biomass
Nitrogen (N) 3 25.17 8.39 4.02 0.0100 22.93 7.64 6.88 0.0003
Boron (B) 1 10.18 10.18 4.87 0.0299 1.07 1.07 0.97 0.3285
N × B 3 10.28 3.43 1.64 0.1859 2.77 0.92 0.83 0.4804
Fruit weight
Nitrogen (N) 3 34.03 11.34 11.40 0.0001 57.67 19.22 16.47 0.0001
Boron (B) 1 62.97 62.97 63.28 0.0001 7.09 7.09 6.07 0.0157
N × B 3 19.21 6.40 6.43 0.0005 0.69 0.23 0.20 0.8980
Main stem length
Nitrogen (N) 3 8938.16 2979.39 6.37 0.0006 2.72 0.91 8.16 0.0001
Boron (B) 1 27.39 27.39 0.06 0.8094 0.00 0.00 0.01 0.9218
N × B 3 5308.35 1769.45 3.78 0.0133 0.56 0.19 1.69 0.1758
Main stem diameter
Nitrogen (N) 3 3.75 1.25 1.68 0.1762 42.60 14.20 6.98 0.0003
Boron (B) 1 0.34 0.34 0.46 0.4979 0.06 0.06 0.03 0.8621
N × B 3 3.50 1.17 1.57 0.2020 4.36 1.45 0.72 0.5455
Number of nodes
Nitrogen (N) 3 100.75 33.58 3.80 0.0131 61.48 20.49 3.00 0.0351
Boron (B) 1 9.31 9.31 1.05 0.3078 8.01 8.01 1.17 0.2821
N × B 3 162.05 54.02 6.10 0.0008 0.84 0.28 0.04 0.9889
Number of branches
Nitrogen (N) 3 1.81 0.60 1.29 0.2823 1.54 0.51 1.01 0.3930
Boron (B) 1 0.03 0.03 0.06 0.7994 2.08 2.08 4.08 0.0464
N × B 3 0.50 0.17 0.36 0.7826 1.74 0.58 1.14 0.3377
Yield
Nitrogen (N) 3 2057324999 685774999 89.95 0.0001 1488760839 496253613 16.74 0.0001
Boron (B) 1 87738296 87738296 11.51 0.00 490040644 490040644 16.53 0.00
N × B 3 101706641 33902213 4.45 0.01 204584902 68194967 2.30 0.10

DF = degree of freedom, SS = sum of squares, MS = mean squares, the p values <0.05 indicate that the corresponding individual and interactive effects are significant, while p values >0.05 denote that the corresponding individual and interactive effects are non-significant.

The highest values of growth attributes such as main stem length, stem diameter and number of nodes per stem and yield were recorded for 270 kg ha-1 N during both years, whereas no N application observed the lowest values of these traits (Fig 1). The growth attributes were not influenced at all by B doses during both years (Table 2).

Fig 1. The impact of different nitrogen doses on growth attributes of grafted watermelon under field conditions.

Fig 1

Table 2. The impact of different boron doses on the pomological attributes of grafted watermelon grown under climatic conditions of Çukurova region.

Boron doses Rind Thickness (mm) Fruit length (cm) Fruit width (cm) Fruit weight (kg) Main stem length (cm) Main stem diameter (mm) Number of nodes Number of branches Yield (kg ha-1)
2018
0 kg ha-1 12.60 b 285.27 b 216.60 b 7.48 b 174.34 8.91 23.06 3.26 46621 b
2 kg ha-1 13.61 a 307.88 a 231.95 a 9.12 a 175.44 9.03 22.44 3.29 49933 a
LSD 0.05 1.00 6.69 4.29 0.40 NS NS NS NS 2849
2019
0 kg ha-1 12.80 b 294.56 212.66 b 7.51 b 2.94 10.94 29.15 3.91 b 36217 b
2 kg ha-1 13.46 a 294.51 218.60 a 8.06 a 2.95 10.90 29.73 4.21 a 44043 a
LSD 0.05 0.65 NS 4.56 0.44 NS NS NS 0.29 3937

Means followed by similar letters within a column are statistically non-significant (p>0.05).

Regarding interactions, the highest values of all growth attributes were recorded 270 kg ha-1 N with both B doses during each year (Table 3).

Table 3. The interactive effect of different nitrogen and boron doses on the pomological attributes of grafted watermelon grown under climatic conditions of Çukurova region.

Treatments Rind thickness (mm) Fruit length (cm) Fruit width (cm) Fruit weight (kg) Main stem length (cm) Main stem diameter (mm) Number of nodes Number of branches Yield (kg ha-1)
2018
N1B1 12.44 cd 277.04 e 208.85 d 6.63 d 154.00 d 9.09 ab 20.25 c 3.42 32581 e
N2B1 12.40 cd 290.59 d 218.84 bc 7.81 bc 165.08 cd 8.72 b 22.00 bc 2.92 43983 c
N3B1 11.27 d 287.91 de 216.72 cd 7.35 cd 185.82 ab 8.67 b 25.09 a 3.36 54470 ab
N4B1 14.17 a 285.77 de 221.99 bc 8.12 bc 193.42 a 9.14 ab 25.08 a 3.33 55454 ab
N1B2 13.55 abc 294.82 cd 224.73 bc 8.32 b 175.00 bc 8.59 b 22.58 bc 3.33 38173 d
N2B2 13.96 ab 310.81 ab 225.55 b 8.25 b 173.08 bc 8.87 ab 23.08 ab 3.17 51787 b
N3B2 14.35 a 319.64 a 240.13 a 10.34 a 167.00 cd 9.20 ab 20.58 c 3.25 53269 ab
N4B2 12.60 bcd 306.26 bc 237.38 a 9.57 a 186.67 ab 9.46 a 23.50 ab 3.42 56505 a
LSD 0.05 1.42 13.38 8.58 0.81 17.64 0.70 2.42 NS 4030
2019
N1B1 14.30 a 283.08 c 203.90 d 6.49 f 2.74 c 9.97 d 28.00 c 3.67 c 29581 d
N2B1 13.23 ab 294.14 bc 211.17 cd 7.38 de 2.85 bc 10.42 bcd 29.08 abc 4.00 abc 35213 d
N3B1 13.36 ab 297.47 abc 216.92 bc 7.58 cde 2.86 bc 11.19 abc 29.36 abc 3.73 bc 36150 cd
N4B1 12.94 b 303.81 ab 219.02 bc 8.58 ab 3.31 a 12.21 a 30.16 ab 4.25 ab 43925 bc
N1B2 12.31 b 282.33 c 205.17 d 6.88 ef 2.71 c 10.14 cd 28.67 bc 4.17 abc 29713 d
N2B2 12.32 b 292.28 bc 218.53 bc 7.85 bcd 3.02 b 10.74 bcd 29.50 abc 4.42 a 43469 bc
N3B2 13.15 ab 292.72 bc 220.91 ab 8.41 abc 2.98 bc 11.26 abc 29.75 abc 4.17 abc 50481 ab
N4B2 13.41 ab 310.73 a 229.79 a 9.10 a 3.09 ab 11.44 ab 31.00 a 4.08 abc 52513 a
LSD 0.05 1.31 15.14 9.13 0.88 0.27 1.16 2.13 0.58 7946

N1 = 0 kg N ha-1, N2 = 90 kg N ha-1, N3 = 180 kg N ha-1, N4 = 270 kg N ha-1, B1 = 0 kg B ha-1, B2 = 2 kg B ha-1, Means followed by similar letters within a column are statistically non-significant (p>0.05).

Pomological attributes

Different N and B doses and their interaction significantly altered various pomological attributes with some exceptions (Table 1). Nitrogen doses significantly altered all pomological attributes except rind thickness during both years. Similarly, B doses also had significant effect on all pomological attributes during both years. Regarding N by B interactions, all pomological attributes were significantly affected during both years (Table 1).

The highest values of pomological attributes such fruit length, width and weight were recorded for 270 kg ha-1 N during both years, whereas no N application observed the lowest values of these traits (Fig 2). The application of 2 kg ha-1 B recorded the highest values of all pomological attributes both years (Table 2).

Fig 2. The impact of different nitrogen doses on pomological attributes of grafted watermelon under field conditions.

Fig 2

Regarding interactions, the highest values of all pomological attributes were recorded for 270 kg ha-1 N with both B doses during each year (Table 3).

Fruit quality attributes

The individual and interactive effect of N and B significantly altered fruit quality attributes during both years (Table 4). Nitrogen doses significantly altered all fruit quality attributes, including sucrose, glucose, fructose, citric acid, tartaric acid, maleic acid and ascorbic acid during both years. Similarly, different B doses had significant effect on all fruit quality attributes during both years, with some exceptions. Regarding N by B interactions, all fruit quality attributes were significantly affected during both years (Table 4).

Table 4. Analysis of variance for different quality traits of grafted watermelon grown under varying nitrogen and boron levels.

2018 2019
Sucrose
Source DF SS MS F value P value SS MS F value P value
Nitrogen (N) 3 20.68 6.89 176.66 0.0001 16.79 5.60 214.77 0.0001
Boron (B) 1 1.94 1.94 49.64 0.0001 4.29 4.29 164.72 0.0001
N × B 3 1.37 0.46 11.71 0.0001 2.22 0.74 28.39 0.0001
Glucose
Nitrogen (N) 3 19.08 6.36 130.56 0.0001 0.23 0.08 78.78 0.0001
Boron (B) 1 0.03 0.03 0.52 0.4796 0.25 0.25 258.47 0.0001
N × B 3 0.34 0.11 2.32 0.1008 0.68 0.23 231.96 0.0001
Fructose
Nitrogen (N) 3 0.10 0.03 4.92 0.0084 1.25 0.42 128.72 0.0001
Boron (B) 1 0.50 0.50 75.16 0.0001 0.00 0.00 0.60 0.4478
N × B 3 0.53 0.18 26.79 0.0001 0.13 0.04 13.72 0.0001
Citric acid
Nitrogen (N) 3 792133.63 264044.54 313.11 0.0001 683016.93 227672.31 278.94 0.0001
Boron (B) 1 11204.11 11204.11 13.29 0.00 26318.95 26318.95 32.25 0.0001
N × B 3 239876.40 79958.80 94.82 0.0001 55285.59 18428.53 22.58 0.0001
Tartaric acid
Nitrogen (N) 3 4859.90 1619.97 219.76 0.0001 1073.24 357.75 77.77 0.0001
Boron (B) 1 59.02 59.02 8.01 0.0093 162.84 162.84 35.40 0.0001
N × B 3 210.73 70.24 9.53 0.0003 595.39 198.46 43.14 0.0001
Maleic acid
Nitrogen (N) 3 260685.56 86895.19 1.87 0.1613 1490809.88 496936.63 27.66 0.0001
Boron (B) 1 26628.38 26628.38 0.57 0.4562 95069.22 95069.22 5.29 0.0304
N × B 3 1069188.29 356396.10 7.68 0.0009 350690.65 116896.88 6.51 0.0022
Ascorbic acid
Nitrogen (N) 3 0.52 0.17 77.44 0.0001 2.75 0.92 696.62 0.0001
Boron (B) 1 0.23 0.23 101.25 0.0001 0.00 0.00 0.01 0.9306
N × B 3 0.57 0.19 84.59 0.0001 0.75 0.25 188.50 0.0001

DF = degree of freedom, SS = sum of squares, MS = mean squares, the p values <0.05 indicate that the corresponding individual and interactive effects are significant, while p values >0.05 denote that the corresponding individual and interactive effects are non-significant.

The highest values of all fruit quality attributes except maleic acid were recorded for 270 kg ha-1 N during both years, whereas no N application observed the lowest values of these traits (Table 5). Similarly, 2 kg ha-1 B observed the highest values of fruit quality attributes during both years (Table 6).

Table 5. The impact of different nitrogen doses on the quality attributes of grafted watermelon grown under climatic conditions of Çukurova region.

Nitrogen doses Sucrose Glucose Fructose Citric acid Tartaric acid Maleic acid Ascorbic acid
2018
0 kg ha-1 1.06 d 1.54 d 3.50 b 378.22 d 28.81 d 2687.72 ab 0.92 d
90 kg ha-1 1.92 c 1.99 c 3.49 b 561.35 c 40.16 c 2841.58 a 1.04 b
180 kg ha-1 2.42 b 2.74 b 3.46 b 695.14 b 49.89 b 2634.28 ab 0.99 c
270 kg ha-1 3.28 a 3.57 a 3.61 a 798.91 a 62.28 a 2609.13 b 1.26 a
LSD 0.05 0.20 0.22 0.08 29.96 2.80 222.32 0.04
2019
0 kg ha-1 2.74 d 1.75 b 2.99 a 454.65 d 23.64 c 2927.60 a 1.13 b
90 kg ha-1 3.14 c 1.91 a 2.64 b 650.05 c 32.70 b 2843.46 a 1.03 c
180 kg ha-1 3.99 b 1.71 c 2.47 d 755.26 b 31.79 b 2363.47 c 1.10 b
270 kg ha-1 4.60 a 1.69 c 2.57 c 847.55 a 39.99 a 2672.93 b 1.76 a
LSD 0.05 0.16 0.03 0.05 29.48 2.21 138.31 0.03

Means followed by similar letters within a column are statistically non-significant (p>0.05).

Table 6. The impact of different boron doses on the quality attributes of grafted watermelon grown under climatic conditions of Çukurova region.

Boron doses Sucrose Glucose Fructose Citric acid Tartaric acid Maleic acid Ascorbic acid
2018
0 kg ha-1 1.92 b 2.49 3.64 a 627.11 a 46.64 a 2722.02 1.13 a
2 kg ha-1 2.41 a 2.43 3.39 b 589.69 b 43.92 b 2664.33 0.97 b
LSD 0.05 0.14 NS 0.05 21.19 1.98 NS 0.03
2019
0 kg ha-1 3.25 b 1.68 b 2.68 648.20 b 29.77 b 2756.37 a 1.25
2 kg ha-1 3.98 a 1.86 a 2.66 705.56 a 34.28 a 2647.36 b 1.25
LSD 0.05 0.11 0.02 NS 20.84 1.56 97.80 NS

Means followed by similar letters within a column are statistically non-significant (p>0.05).

Regarding interactions, the highest values of all fruit quality attributes were recorded for 270 kg ha-1 N with both B doses during each study year (Table 7).

Table 7. The impact of nitrogen by boron doses interaction on the fruit quality attributes of grafted watermelon grown under climatic conditions of Çukurova region.

Treatments Sucrose Glucose Fructose Citric acid Tartaric acid Maleic acid Ascorbic acid
2018
N1B1 0.57 f 1.42 e 3.75 a 249.17 e 32.33 f 2536.37 bc 0.78 e
N2B1 1.74 e 1.98 cd 3.66 ab 652.71 c 42.04 e 3175.91 a 1.22 b
N3B1 2.47 c 2.85 b 3.37 de 756.61 b 52.89 c 2598.72 bc 1.09 c
N4B1 2.91 b 3.71 a 3.77 a 849.96 a 59.31 b 2577.08 bc 1.45 a
N1B2 1.55 e 1.66 de 3.25 e 507.26 d 25.29 g 2839.07 b 1.05 c
N2B2 2.09 d 2.01 c 3.32 de 469.98 d 38.28 e 2507.24 c 0.86 d
N3B2 2.36 cd 2.63 b 3.55 bc 633.66 c 46.89 d 2669.83 bc 0.89 d
N4B2 3.64 a 3.44 a 3.44 cd 747.87 b 65.24 a 2641.17 bc 1.06 c
LSD 0.05 0.28 0.32 0.11 42.38 3.96 314.41 0.06
2019
N1B1 2.48 f 1.64 e 3.01 a 354.38 e 26.21 d 3016.41 a 1.01 e
N2B1 3.15 de 1.74 d 2.75 b 640.17 c 32.46 c 2996.14 a 1.02 e
N3B1 3.34 d 1.49 g 2.45 e 757.27 b 22.67 b 2461.85 d 1.35 c
N4B1 4.03 c 1.85 c 2.50 de 840.98 a 37.75 e 2551.09 cd 1.64 b
N1B2 2.99 e 1.86 c 2.98 a 554.93 d 21.07 e 2838.79 ab 1.24 d
N2B2 3.13 de 2.08 a 2.53 d 659.93 c 32.94 c 2690.78 bc 1.05 e
N3B2 4.64 b 1.94 b 2.49 de 753.24 b 40.90 a 2265.10 e 0.84 f
N4B2 5.17 a 1.54 f 2.64 c 854.12 a 42.22 a 2794.76 b 1.88 a
LSD 0.05 0.23 0.04 0.08 41.69 3.13 195.62 0.05

N1 = 0 kg N ha-1, N2 = 90 kg N ha-1, N3 = 180 kg N ha-1, N4 = 270 kg N ha-1, B1 = 0 kg B ha-1, B2 = 2 kg B ha-1, Means followed by similar letters within a column are statistically non-significant (p>0.05).

Discussion

Individual and interactive effects of N and B altered growth, yield, pomological and fruit quality attributes. As hypothesized, increasing doses of N and B improved growth, pomological and fruit quality attributes. The highest values of growth, pomological and fruit quality attributes were recorded for the highest N and B doses used in the current study. These can be owed to the continuous availability of both nutrients throughout the growing season, which resulted in proper functioning, metabolism and nutrition. Collectively all metabolic processes improved growth, pomological and fruit quality attributes of grafted watermelon in the current study.

Stem length or plant height is an important character related to plant productivity [34]. Main stem length was increased with increasing N doses. This could be attributed to the ability of N treatments to enhance plant growth via promoting cellular division and nutrients’ uptake from soils [35]. Chlorophyll is an essential biomolecule for photon absorption, transmission, transportation and photosynthetic rate (Pn) in leaves [36]. Lawlor et al. [37] reported that increasing N fertilizer can restore the chlorophyll in plants. Thus, improved growth attributes are owed to higher chlorophyll synthesis with higher N dose in the current study.

Plants require N in large quantity for optimum growth and development. Nitrogen is necessary for various metabolic processes of crop plants. Chlorophyll synthesis and photosynthesis are directly influenced by N [29, 3841]. Plant growth is poor under low N availability as it is part of amino acids, nucleic acid, proteins, chlorophyll and hormones [42]. Nonetheless, photosynthesis, flowering and fruit development are positively influenced by optimum N availability resulting in higher crop yields [29, 43, 44]. Improved growth attributes are owed to these processes in the current study.

Boron is involved in numerous physiological processes of plants [20, 45, 46]. Principally, cell wall structural integration, and linkage of B with pectic polysaccharide rhamnogalacturonan regulate porosity and tensile strength of the cell wall [19]. However, limitation or excess of B adversely affect plant growth [2124]. The obvious response of B-deficiency in several crops is inhibition of root growth because of reduced cell division [47]. Moreover, long-term deficient B condition provokes lipid peroxidation and reduces the activity of antioxidant enzymes [20, 23].

Composition of cereal grains is significantly altered by N [48], whereas sugar concentrations and conversion of simple sugars and complex carbohydrates is also regulated by N availability [49]. Free amino acid concentrations of cereal grain is significantly affected by N supply [5052]. Concentrations of sugars in tubers may be increased by 100% in potatoes under N-deficiency [53]. Similarly, non-availability of N results in lower concentration of reducing sugars [54]. Increased N fertilizer has also been shown to cause a rise in free amino acid concentrations [55]. The improvement in fruit quality attributes, particularly of sugars is directly linked with N availability. Since both B doses resulted in similar fruit quality attributes with both B doses, it is concluded that N is the main determinant of fruit quality attributes rather than B.

Data Availability

All relevant data are within the paper.

Funding Statement

This study was partially supported by Çukurova University Scientific Research Projects Coordination Unit (Project No: FBA-2018- 10970). There were no additional external funding involved in the study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1.Barbet-Massin C, Giuliano S, Alletto L, Daydé J, Berger M. Nitrogen limitation alters biomass production but enhances steviol glycoside concentration in Stevia rebaudiana bertoni. PLoS One. 2015. 10.1371/journal.pone.0133067 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Rodrigues MÂ, Afonso S, Ferreira IQ, Arrobas M. Response of stevia to nitrogen fertilization and harvesting regime in northeastern Portugal. Arch Agron Soil Sci. 2017. 10.1080/03650340.2016.1230272 [DOI] [Google Scholar]
  • 3.Pal PK, Mahajan M, Prasad R, Pathania V, Singh B, Ahuja PS. Harvesting regimes to optimize yield and quality in annual and perennial Stevia rebaudiana under sub-temperate conditions. Ind Crops Prod. 2015. [Google Scholar]
  • 4.Sun Y, Hou M, Mur LAJ, Yang Y, Zhang T, Xu X, et al. Nitrogen drives plant growth to the detriment of leaf sugar and steviol glycosides metabolisms in Stevia (Stevia rebaudiana Bertoni). Plant Physiol Biochem. 2019;141: 240–249. 10.1016/j.plaphy.2019.06.008 [DOI] [PubMed] [Google Scholar]
  • 5.Yadav AK, Singh S, Dhyani D, Ahuja PS. A review on the improvement of stevia [Stevia rebaudiana (Bertoni)]. Can J Plant Sci. 2011;91: 1–27. [Google Scholar]
  • 6.Aires A, Rosa E, Carvalho R. Effect of nitrogen and sulfur fertilization on glucosinolates in the leaves and roots of broccoli sprouts (Brassica oleracea var. italica). J Sci Food Agric. 2006;86: 1512–1516. [Google Scholar]
  • 7.Ibrahim MH, Jaafar HZE, Rahmat A, Rahman ZA. Effects of nitrogen fertilization on synthesis of primary and secondary metabolites in three varieties of kacip fatimah (Labisia pumila Blume). Int J Mol Sci. 2011;12: 5238–5254. 10.3390/ijms12085238 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Goodall AJ, Kumar P, Tobin AK. Identification and expression analyses of cytosolic glutamine synthetase genes in barley (Hordeum vulgare L.). Plant Cell Physiol. 2013;54: 492–505. 10.1093/pcp/pct006 [DOI] [PubMed] [Google Scholar]
  • 9.Tafteh A, Sepaskhah AR. Application of HYDRUS-1D model for simulating water and nitrate leaching from continuous and alternate furrow irrigated rapeseed and maize fields. Agric Water Manag. 2012;113: 19–29. [Google Scholar]
  • 10.Shahrokhnia MH, Sepaskhah AR. Effects of irrigation strategies, planting methods and nitrogen fertilization on yield, water and nitrogen efficiencies of safflower. Agric Water Manag. 2016;172: 18–30. [Google Scholar]
  • 11.Kant S, Bi Y-M, Rothstein SJ. Understanding plant response to nitrogen limitation for the improvement of crop nitrogen use efficiency. J Exp Bot. 2011;62: 1499–1509. 10.1093/jxb/erq297 [DOI] [PubMed] [Google Scholar]
  • 12.Liu P. The future of food and agriculture: Trends and challenges. Food Agric Organ United Nations. 2015. [Google Scholar]
  • 13.Chen X, Cui Z, Fan M, Vitousek P, Zhao M, Ma W, et al. Producing more grain with lower environmental costs. Nature. 2014;514: 486–489. 10.1038/nature13609 [DOI] [PubMed] [Google Scholar]
  • 14.Zhu S, Vivanco JM, Manter DK. Nitrogen fertilizer rate affects root exudation, the rhizosphere microbiome and nitrogen-use-efficiency of maize. Appl Soil Ecol. 2016;107: 324–333. [Google Scholar]
  • 15.Camargo JA, Alonso Á. Ecological and toxicological effects of inorganic nitrogen pollution in aquatic ecosystems: a global assessment. Environ Int. 2006;32: 831–849. 10.1016/j.envint.2006.05.002 [DOI] [PubMed] [Google Scholar]
  • 16.Sigee D. Freshwater microbiology: biodiversity and dynamic interactions of microorganisms in the aquatic environment. John Wiley & Sons; 2005. [Google Scholar]
  • 17.Beman JM, Arrigo KR, Matson PA. Agricultural runoff fuels large phytoplankton blooms in vulnerable areas of the ocean. Nature. 2005;434: 211–214. 10.1038/nature03370 [DOI] [PubMed] [Google Scholar]
  • 18.Marschner P. Marschner’s Mineral Nutrition of Higher Plants: Third Edition. Marschner’s Mineral Nutrition of Higher Plants: Third Edition. 2011. 10.1016/C2009-0-63043-9 [DOI] [Google Scholar]
  • 19.O’Neill MA, Ishii T, Albersheim P, Darvill AG. Rhamnogalacturonan II: structure and function of a borate cross-linked cell wall pectic polysaccharide. Annu Rev Plant Biol. 2004;55: 109–139. 10.1146/annurev.arplant.55.031903.141750 [DOI] [PubMed] [Google Scholar]
  • 20.Brown PH, Bellaloui N, Wimmer MA, Bassil ES, Ruiz J, Hu H, et al. Boron in plant biology. Plant Biol. 2002;4: 205–223. [Google Scholar]
  • 21.Gupta U, Solanki H. Impact of boron deficiency on plant growth. Int J Bioassays. 2013;2: 1048–1050. [Google Scholar]
  • 22.Landi M, Margaritopoulou T, Papadakis IE, Araniti F. Boron toxicity in higher plants: an update. Planta. 2019;250: 1011–1032. 10.1007/s00425-019-03220-4 [DOI] [PubMed] [Google Scholar]
  • 23.Landi M, Degl’Innocenti E, Pardossi A, Guidi L. Antioxidant and photosynthetic responses in plants under boron toxicity: a review. Am J Agric Biol Sci. 2012;7: 255–270. [Google Scholar]
  • 24.Tombuloglu H, Tombuloglu G, Sakcali MS, Turkan A, Hakeem KR, Alharby HF, et al. Proteomic analysis of naturally occurring boron tolerant plant Gypsophila sphaerocephala L. in response to high boron concentration. J Plant Physiol. 2017;216: 212–217. 10.1016/j.jplph.2017.06.013 [DOI] [PubMed] [Google Scholar]
  • 25.Ozturk M, Sakcali S, Gucel S, Tombuloglu H. Boron and plants. Plant adaptation and phytoremediation. Springer; 2010. pp. 275–311. [Google Scholar]
  • 26.Shireen F, Nawaz MA, Xiong M, Ahmad A, Sohail H, Chen Z, et al. Pumpkin rootstock improves the growth and development of watermelon by enhancing uptake and transport of boron and regulating the gene expression. Plant Physiol Biochem. 2020;154: 204–218. 10.1016/j.plaphy.2020.06.003 [DOI] [PubMed] [Google Scholar]
  • 27.Colla G, Rouphael Y, Mirabelli C, Cardarelli M. Nitrogen‐use efficiency traits of mini‐watermelon in response to grafting and nitrogen‐fertilization doses. J Plant Nutr Soil Sci. 2011;174: 933–941. [Google Scholar]
  • 28.Torun AA, Solmaz İ, Duymuş E, Aydın O, Cenkseven Ş, Yalçınkaya A, et al. Effect of different doses of nitrogen and potassium fertilization on yield and nutrient uptake in grafted watermelon growing in çukurova region conditions. Int J Agric Nat Sci. 2018;1: 228–232. [Google Scholar]
  • 29.Nawaz MA, Wang L, Jiao Y, Chen C, Zhao L, Mei M, et al. Pumpkin rootstock improves nitrogen use efficiency of watermelon scion by enhancing nutrient uptake, cytokinin content, and expression of nitrate reductase genes. Plant Growth Regul. 2017;82: 233–246. 10.1007/s10725-017-0254-7 [DOI] [Google Scholar]
  • 30.Moustafa-Farag M, Bingsheng F, Malangisha Guy K, Hu Z, Yang J, Zhang M. Activated antioxidant enzymes-reduced malondialdehyde concentration, and improved mineral uptake-promoted watermelon seedlings growth under boron deficiency. J Plant Nutr. 2016;39: 1989–2001. [Google Scholar]
  • 31.Boualem A, Lemhemdi A, Sari M-A, Pignoly S, Troadec C, Abou Choucha F, et al. The andromonoecious sex determination gene predates the separation of Cucumis and Citrullus genera. PLoS One. 2016;11: e0155444. 10.1371/journal.pone.0155444 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Shapiro SS, Wilk MB. An analysis of variance test for normality (complete samples). Biometrika. 1965;52: 591–611. [Google Scholar]
  • 33.Steel R., Torrei J, Dickey D. Principles and Procedures of Statistics A Biometrical Approach. A Biometrical Approach. 1997. [Google Scholar]
  • 34.Wysocki DJ, Horneck DA, Lutcher LK. Irrigated and dryland canola. 2007. [Google Scholar]
  • 35.Ullah I, Ali N, Durrani S, Shabaz MA, Hafeez A, Ameer H, et al. Effect of different nitrogen levels on growth, yield and yield contributing attributes of wheat. Int J Sci Eng Res. 2018;9: 595. [Google Scholar]
  • 36.Baig MJ, Anand A, Mandal PK, Bhatt RK. Irradiance influences contents of photosynthetic pigments and proteins in tropical grasses and legumes. Photosynthetica. 2005;43: 47–53. [Google Scholar]
  • 37.Lawlor DW. Carbon and nitrogen assimilation in relation to yield: mechanisms are the key to understanding production systems. J Exp Bot. 2002;53: 773–787. [PubMed] [Google Scholar]
  • 38.Luo J, Li H, Liu T, Polle A, Peng C, Luo Z-B. Nitrogen metabolism of two contrasting poplar species during acclimation to limiting nitrogen availability. J Exp Bot. 2013;64: 4207–4224. 10.1093/jxb/ert234 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Takei K, Sakakibara H, Taniguchi M, Sugiyama T. Nitrogen-dependent accumulation of cytokinins in root and thetranslocation to leaf: Implication of cytokinin species that induces geneexpression of maize responseregulator. Plant Cell Physiol. 2001;42: 85–93. 10.1093/pcp/pce009 [DOI] [PubMed] [Google Scholar]
  • 40.Tischner R. Nitrate uptake and reduction in higher and lower plants. Plant Cell Environ. 2000;23: 1005–1024. [Google Scholar]
  • 41.Colla G, Suarez CMC, Cardarelli M, Rouphael Y. Improving nitrogen use efficiency in melon by grafting. HortScience. 2010;45: 559–565. [Google Scholar]
  • 42.Masclaux-Daubresse C, Daniel-Vedele F, Dechorgnat J, Chardon F, Gaufichon L, Suzuki A. Nitrogen uptake, assimilation and remobilization in plants: challenges for sustainable and productive agriculture. Ann Bot. 2010;105: 1141–1157. 10.1093/aob/mcq028 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Prinsi B, Negri AS, Pesaresi P, Cocucci M, Espen L. Evaluation of protein pattern changes in roots and leaves of Zea mays plants in response to nitrate availability by two-dimensional gel electrophoresis analysis. BMC Plant Biol. 2009;9: 1–17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Curci PL, Cigliano RA, Zuluaga DL, Janni M, Sanseverino W, Sonnante G. Transcriptomic response of durum wheat to nitrogen starvation. Sci Rep. 2017;7: 1–14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Dell B, Huang L. Physiological response of plants to low boron Plant Soil. 1997;193: 103–120. [Google Scholar]
  • 46.Shireen F, Nawaz MA, Chen C, Zhang Q, Zheng Z, Sohail H, et al. Boron: functions and approaches to enhance its availability in plants for sustainable agriculture. Int J Mol Sci. 2018;19: 1856. 10.3390/ijms19071856 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Goldbach HE, Yu Q, Wingender R, Schulz M, Wimmer M, Findeklee P, et al. Rapid response reactions of roots to boron deprivation. J Plant Nutr Soil Sci. 2001;164: 173–181. [Google Scholar]
  • 48.Shewry PR, Tatham AS, Halford NG. Nutritional control of storage protein synthesis in developing grain of wheat and barley. Plant Growth Regul. 2001;34: 105–111. [Google Scholar]
  • 49.Halford NG, Curtis TY, Muttucumaru N, Postles J, Mottram DS. Sugars in crop plants. Ann Appl Biol. 2011;158: 1–25. [Google Scholar]
  • 50.Muttucumaru N, Halford NG, Elmore JS, Dodson AT, Parry M, Shewry PR, et al. Formation of high levels of acrylamide during the processing of flour derived from sulfate-deprived wheat. J Agric Food Chem. 2006;54: 8951–8955. 10.1021/jf0623081 [DOI] [PubMed] [Google Scholar]
  • 51.Lea PJ, Sodek L, Parry MAJ, Shewry PR, Halford NG. Asparagine in plants. Ann Appl Biol. 2007;150: 1–26. [Google Scholar]
  • 52.Curtis TY, Muttucumaru N, Shewry PR, Parry MA, Powers SJ, Elmore JS, et al. Evidence for genetic and environmental effects on free amino acid levels in wheat grain: implications for acrylamide formation during processing. J Agric Food Chem. 2009;57: 1013–1021. [DOI] [PubMed] [Google Scholar]
  • 53.De Wilde T, De Meulenaer B, Mestdagh F, Govaert Y, Vandeburie S, Ooghe W, et al. Influence of fertilization on acrylamide formation during frying of potatoes harvested in 2003. J Agric Food Chem. 2006;54: 404–408. 10.1021/jf0521810 [DOI] [PubMed] [Google Scholar]
  • 54.Kumar D, Singh BP, Kumar P. An overview of the factors affecting sugar content of potatoes. Ann Appl Biol. 2004;145: 247–256. [Google Scholar]
  • 55.Eppendorfer WH, Bille SW. Free and total amino acid composition of edible parts of beans, kale, spinach, cauliflower and potatoes as influenced by nitrogen fertilisation and phosphorus and potassium deficiency. J Sci Food Agric. 1996;71: 449–458. [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

All relevant data are within the paper.


Articles from PLoS ONE are provided here courtesy of PLOS

RESOURCES