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Original article
08 2022
:34;
102190
doi:
10.1016/j.jksus.2022.102190

Screening of chickpea genotypes for boron biofortification potential

Department of Agronomy, Bahauddin Zakariya University, Multan, Pakistan
College of Agriculture, Bahauddin Zakariya University, Bahadur Sub-Campus Layyah, Pakistan
Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 22452, Riyadh, Saudi Arabia
School of Veterinary and Life Sciences, Murdoch University, 90 South Street, Murdoch, WA 6150, Australia

⁎Corresponding author at: Department of Agronomy, Bahauddin Zakariya University, Multan, Pakistan. mubashiragr@gmail.com (Mubshar Hussain)

Disclaimer:
This article was originally published by Elsevier and was migrated to Scientific Scholar after the change of Publisher.

Peer review under responsibility of King Saud University.

Abstract

Background

Malnutrition is a significant threat to mankind and deficiency of important minerals like boron (B) exert negative impacts on human health mostly in developing and least developed countries. Chickpea is an important legume with wide consumption in human diet due to easily digestible dietary protein and grown. Chickpea is mostly grown in arid and semi-arid regions of Pakistan. The B-deficiency in these areas not only decreases chickpea productivity, but also results lowers B concentration in grains. Different chickpea genotypes are capable of perform differently due to their divergent genetic makeup under stressful environmental conditions. Therefore, this field study screened different chickpea genotypes to improve yield and B biofortification.

Methods

For this purpose 20 ‘desi’ (i.e., ‘TG-1430’, ‘Parbat’, ‘TG-1616’, ‘TG-1620’, ‘05A028’, ‘TG-1601’, ‘TG-1623’, ‘Thal-2006’, ‘TG-1218’, ‘TG-1513’, ‘Chattan’, ‘BK-2011’, ‘TG-1500’, ‘NIAB-2016’, ‘GGP-1456’, ‘TG-1618’, ‘TG-1619’, ‘Bittle-2016’, ‘TG-1415’ and ‘Punjab-2008’) and 06 ‘kabuli’ (i.e., ‘TGK-228’, ‘TGK-1767’, ‘TGK-1802’, ‘NOOR-2009’, ‘TGK-1761’ and ‘TGK-1805’) chickpea genotypes were sown under 0 or 1 kg B ha−1 as soil application.

Results

Results indicated that B application improved the growth, nodulation, yield and grains B concentrations of all genotypes; however, genotype significantly differed in their response. Of the 20 ‘desi’ genotypes ‘Punjab-2008’ recorded the highest leaf area index, leaf area duration, crop growth rate, nodulation, yield and related traits under B application. However, genotypes ‘BK-2011’, ‘TG-1500’ and ‘NIAB-2016’ had higher grains B content under 1 kg ha−1 B application. Similarly, ‘kabuli genotypes’, i.e., ‘TGK-1761’ and ‘TGK-1802’ recorded higher nodulation, while ‘NOOR-2009’ had higher leaf area index, leaf area duration, crop growth rate, 1000-grain weight, grain yield and biological yield with 1 kg ha−1 B application compared to the rest of the ‘kabuli’ genotypes included in the study. The highest grain B concentration was recorded for ‘TGK-1767’ among ‘kabuli’ genotypes.

Conclusion

In conclusion, ‘desi’ genotype ‘Punjab-2008’ and ‘kabuli’ genotype ‘NOOR-2009’ should be grown under 1 kg ha−1 B application to get higher productivity and B biofortification. The genotypes which accumulated more B in their seeds should be included in future breeding programs to produce B-rich grains for reducing malnutrition.

Keywords

Genotypes
Biofortification
Grain yield
Nodulation
Grains boron concentration
1

1 Introduction

Malnutrition is a significant threat to mankind and affects >50% of the population of the world. Mostly pregnant women, and the kids below five-years age suffer from malnutrition, particularly in developing countries (Alloway, 2008; Ritchie and Roser, 2017). Micronutrients are equally important as macronutrients and required in very minute amount (Kalsoom et al., 2020; Nadeem et al., 2020). Boron (B) deficiency is critical among all micronutrients’ deficiencies, and regarded as a leading cause of a number of diseases in children residing in the developing countries (Hussain et al., 2020). Boron deficiency has been reported from ∼80 countries which exerts negative impacts on >132 plant species (Brestic et al., 2021; Hossain et al., 2021; Hua et al., 2016). The B-deficiency is mostly observed in calcareous soils that exerts negative effects on crop yields (Rashid et al., 2011; Waraich et al., 2011). Most of the Pakistani soils are calcareous in nature and deficient in micronutrients, particularly B (Rashid and Ryan, 2004). The B-deficiency status in Pakistani soils is alarming as 65% of the soils are B-deficient (Rashid and Ryan, 2004).

Boron is an essential micronutrient, structural component of plant cell wall, and plays an important role in the integrity of membrane in plants (Bassil et al., 2004; Maitra et al., 2021; Qureshi et al., 2021). It also plays an important role in transportation, photosynthetic activity and metabolism of indole acetic acid (Dordas and Brown, 2000; Hussain et al., 2012; Wang et al., 2007). Several studies reported that B application through different methods increased yield of different crops, including chickpea (Cicer arietinum L.) (Mehboob et al., 2022, 2021), cotton (Gossypium hirsutum L.) (Atique-ur-Rehman et al., 2020; Roberts et al., 2000), rice (Oryza sativa L.) (David et al., 2005; Rashid and Ryan, 2004), sunflower (Helianthus annus L.) (Ariraman et al., 2020; Ceyhan et al., 2008) and mungbean (Vigna radiata L.) (Laxmi et al., 2020). Boron is required in less amount; hence, the range between B-deficiency and toxicity is extremely narrow (Yau and Ryan, 2008). The B-deficiency disrupts biochemical, physiological, and cellular functions of plants which cause malnutrition problems and impairs plant growth. Boron-deficiency is mostly observed in reproductive stage of plants rather than vegetative stage and affects flowering, pollination, fruit setting, seed setting and grain filling (Islam et al., 2017). However B-deficiency in wheat (Triticum aestivum L.) increased number of open spikelets and decrease number of grains per spike which negatively affected grain setting (Tahir et al., 2009). The B-toxicity has been reported to negativelt affect crop production in arid and semi-arid regions of the world (Ahmad et al., 2013; Çatav et al., 2018). Boron application at higher level (toxicity) proved toxic for growth and productivity of chickpea (Hussain et al., 2020).

Chickpea is an annual grain legume grown in arid and semi-arid regions in Pakistan. It is a good source of easily digestible dietary proteins (22–28%), and contains significant amount of carbohydrates, fats, crude fiber and minerals (Foyer et al., 2016). The ‘kabuli’ and ‘desi’ chickpea genotypes are mostly grown around the world. The total cultivated area under ‘desi’ genotypes is 80–85%, while the remaining 15–20% area is cultivated with ‘kabuli’ genotypes in indo-Pakistan region. Chickpea requires very low amount of water; thus, arid, and semi-arid regions are optimum for its cultivation. Biofortification is the technique of integrating minerals into edible parts of crops. It offers a justifiable and economic way of increasing the density of minerals/micronutrients in important staple crops (Hossain et al., 2021; Mehboob et al., 2021). Addition of nutrients in edible parts of plants will help to control malnutrition and improve food quality (Mao et al., 2014; White and Broadley, 2009). Soil application of B at sowing may improve chickpea growth, nodulation and productivity (Mehboob et al., 2021). Soil application of B significantly improved physiological parameters and fiber quality of cotton (Atique-ur-Rehman et al., 2020).

All crops and their varieties may vary in the ability to uptake B from soils. This variation is primarily directed by their genetic structure, although environmental conditions and plant morphology also play their role in this variation. Therefore, this field study was designed to screen the available chickpea germplasm (both ‘desi’ and ‘kabuli’ genotypes) to find the most responsive genotypes for B uptake and translocations to grains. All collected germplasm was sown with and without B application to evaluate the effect of B on growth, nodulation, yield, and grain-B concentration. The better performing genotypes (both ‘desi’ and ‘kabuli’) will be further evaluated under different B application methods to determine the most reliable approach of getting higher chickpea yield and grain-B contents.

2

2 Materials and methods

2.1

2.1 Plant material

Seeds of 26 frequently cultivated chickpea genotypes, i.e., ‘TGK-1767’, ‘TGK-1802’, ‘NOOR-2009’, ‘TGK-1761’, ‘TGK-1805’, ‘TGK-228’, ‘TG-1430’, ‘Parbat’, ‘TG-1616’, ‘TG-1620’, ‘05A028’, ‘TG-1601’, ‘TG-1623’, ‘Thal-2006’, ‘TG-1218’, ‘TG-1513’, ‘Chattan’, ‘BK-2011’, ‘TG-1500’, ‘NIAB-2016’, ‘GGP-1456’, ‘TG-1618’, ‘TG-1619’, ‘Bittle-2016’, ‘TG-1415’ and ‘Punjab-2008’ were obtained from Arid Zone Research Institute (AZRI), Bakkhar, Pakistan and used in the study. Six genotypes, i.e., ‘TGK-1767’, ‘TGK-1761’, ‘TGK-1805’, ‘TGK-228’, ‘TGK-1802’ and ‘NOOR-2009’ were ‘kabuli’, while rest of the genotypes were ‘desi’. Boric acid (Merck, Germany, 17% B) was used as B source and applied at the time of sowing.

2.2

2.2 Description of experimental site

This study was conducted at Bahauddin Zakariya University, Bahadur Sub Campus, Layyah, Pakistan during Rabi season of 2018–2019. Before sowing, soil analysis was performed to assess the initial soil fertility status. Soil was sandy-loam with 3.54 dS m−2 EC, 8.00 pH, 30.0% saturation percentage, 0.57% organic matter, 5.40 mg kg−1 available phosphorus, 130.00 mg kg−1 available potassium and 0.57 mg kg−1 available B.

2.3

2.3 Experimental details

Seeds of all chickpea genotypes were sown on well-prepared seedbed under two B application levels, i.e., 0 and 1 kg B ha−1. Boric acid was used as a source of B. The experiment was laid out according to randomized complete block design with factorial arrangement. Boron levels were kept in the main plots, whereas genotypes were randomized in sub plots. All treatment had three replications with a net plot size of 4.0 m × 1.8 m.

2.4

2.4 Crop husbandry

Pre-soaking irrigation (locally called rouni) of 10 cm was applied to bring soil under optimum moisture level for seedbed preparation. When soil reached to workable moisture level, seedbed was prepared by cultivating the field two times with tractor drawn cultivator followed by planking. Chickpea was sown on November 01, 2018 by hand drill using seed rate of 80 kg ha−1 in 45 cm spaced rows. Before sowing 40 kg ha−1 nitrogen (N) and 80 kg ha−1 phosphorous (P) was applied using urea and triple superphosphate as sources of N and P, respectively. In total 4 irrigations were applied to fulfill moisture needs of chickpea. Weeds were controlled manually. All agronomic practices were uniform from sowing to harvesting. Mature crop was harvested on April 10, 2019.

2.5

2.5 Data collection

2.5.1

2.5.1 Growth attributes

To measure leaf area index (LAI) and crop growth rate (CGR), plants from 1 m2 area were harvested at 45 days after sowing (DAS) and second data were recorded at 90 DAS. Leaves were detached from the stem and their area was measured by using leaf area meter (DT Area Meter, Model MK2, Delta T Devices, Cambridge, UK). The LAI was computed by the formula given by Watson (1947). L A I = Leafarea Groundarea

Fresh weight of the plants harvested from 1 m2 was measured by using weight balance and then samples were dried under sunlight for 48 h. After sun drying the samples were oven-dried at 70 °C for 72 h under thermostatic blast drying oven. Afterwards, oven-dried samples were weighed. The formula given by Hunt, (1982) was used to calculate CGR. C G R = ( W 2 - W 1 ) / ( t 2 - t 1 )

Here W2 is dry weight at 90 DAS while W1 is dry weight taken at 45 DAS. Moreover, t2 and t1 are the time interval during both data.

Leaf area duration was calculated by using Hunt (1982) suggested formula. L A D = ( L A I 2 + L A I 1 ) / 2 × ( t 2 - t 1 )

LAI2 and LAI1 are leaf area index at 90 DAS and 45 DAS where t2 − t1 are time interval during both data.

Net assimilation rate (NAR) was calculated by using following formula of Beadle (1985). N A R = TDM LAD where TDM = total dry matter.

2.5.2

2.5.2 Yield traits

When crop reached at harvest maturity, 10 plants were harvested randomly from each genotype to record yield-related traits. Plant height was measured with a measuring tape and averaged. The nodules population was counted from each plant and averaged to record number of nodules per plant. For number of branches and pods per plant, number of branches and pods on each plant were counted carefully and averaged. The pods were threshed manually, and 1000 grains from each experimental unit were counted and weight to record 1000-grain weight. The plants from 1 m2 area were harvested, pods were removed and threshed manually to calculate grain yield. These yield was then converted into tones ha−1. All remaining plant parts were put under shade for sun drying for 48 h. After complete drying, the samples were weighed, and grain weight was added to record biological yield m2. Harvest index was taken as: H a r v e s t i n d e x ( % ) = Grain y i e l d Biological y i e l d

2.5.3

2.5.3 Grains boron analysis

For B analysis, grains sample was collected at harvest. Grain samples were dried in oven at 70 °C. Afterwards, 1 g sample from each treatment was taken in a porcelain crucible and kept in muffle at 550 °C for 6 h. Extraction of ashed samples was done by 10 ml of 0.36 N H2SO4 for 1 h. Extracted samples were then filtered with Whatman Number 1 filter paper and transferred in 50 ml plastic transparent bottles and volume was made 50 ml by adding distilled water. The buffer solution (ammonium acetate 250 ml, EDTA 15 ml dissolve in 400 ml distill water and then add slowly 125 ml acetic acid) and azomethine solution containing (azomethine-H 0.45 g and L-ascorbic acid 1 g in 100 ml water) were added to the filterate. The filtrate of 1 ml extracted solution was mixed with 2 ml of buffer solution and 2 ml of azomethine-H solution. This solution was kept for 45 min to develop color and the B concentration in each sample was recorded by spectrophotometer at 420 nm.

2.6

2.6 Statistical analysis

The data were checked for homogeneity of variance and normality. The collected data were subjected to two-way analysis of variance (ANOVA) to check the overall significance of data by using statistical package Statistix 8.1 (Analytical Software, USA). However, the difference among treatments means were compared using least significant difference (LSD) test at 95% probability level (Steel et al., 1997).

3

3 Results

Chickpea genotypes, B application and their interaction had highly significant effect on LAI, LAD, CGR and NAR, whereas interactive effect remained non-significant for CGR (Table 1). Overall, ‘desi’ genotypes recorded higher LAI, LAD, CGR and NAR during whole growing season than ‘kabuli' genotypes. With respect to B application, B applied at 1 kg ha−1 responded positively and increased LAI, LAD and CGR against no B application (Figs. 1–3). The ‘desi’ genotype ‘Punjab-2008’ and ‘kabuli’ genotype ‘NOOR-2009’ recorded higher LAI and LAD with 1 kg B ha−1 application compared to the rest of ‘desi’ and ‘kabuli’ genotypes at 45 and 90 DAS (Figs. 1 and 2). Moreover, ‘Thal-2006’ recorded higher NAR 1 kg B ha−1 application compared to the rest of the genotypes (Fig. 3).

Table 1 Analysis of variance of yield related traits and B-grain concentration of different chickpea genotypes (06 kabuli vs 20 desi treated with B levels (0 vs 1 kg ha−1).
Plant height (cm) Number of nodules per plant
SOV df SS MS P value SS MS P value
Chickpea genotypes (V) 25 1088.92 43.56 0.0000* 1548.41 61.94 0.0210*
Boron levels (B) 1 519.91 519.91 0.0000* 407.08 407.08 0.0008*
V × B 25 414.03 16.56 0.0040* 1328.26 53.13 0.0665NS
Number of branches per plant Number of pods per plant
Chickpea genotypes (V) 25 61.46 2.46 0.0166* 915.81 36.62 0.0000*
Boron levels (B) 1 38.61 38.61 0.0000* 641.89 641.89 0.0000*
V × B 25 60.54 2.42 0.0189* 948.10 37.92 0.0000*
1000 grains weight (g) Grain yield (t ha−1)
Chickpea genotypes (V) 25 4298.0 171.9 0.0000* 3.65 0.14 0.0002*
Boron levels (B) 1 18734.8 18734.8 0.0000* 4.18 4.18 0.0000*
V × B 25 726.8 29.1 0.0007* 1.00 0.04 0.7979NS
Biological yield (t ha−1) Harvest index (%)
Chickpea genotypes (V) 25 18.36 0.73 0.0000* 43.54 1.74 0.1894NS
Boron levels (B) 1 23.41 23.41 0.0000* 24.17 24.17 0.0001*
V × B 25 4.66 0.19 0.5786NS 36.47 1.46 0.3809NS
B grain contents (mg kg−1) Leaf area duration (day)
Chickpea genotypes (V) 25 5633.9 225.4 0.0000* 3066.51 122.66 0.0000*
Boron levels (B) 1 68467.5 68467.5 0.0000* 478.24 478.24 0.0000*
V × B 25 2473.0 98.9 0.0000* 266.84 10.67 0.0000*
Leaf area index at 45 DAS Leaf area index at 90 DAS
Chickpea genotypes (V) 25 7.80 0.31 0.0000* 7.60 0.30 0.0000*
Boron levels (B) 1 1.56 1.56 0.0000* 0.87 0.87 0.0000*
V × B 25 0.84 0.03 0.0000* 0.57 0.23 0.0000*
Crop growth rate (g m−2 day−1) Net assimilation rate (g m−2 day−1)
Chickpea genotypes (V) 25 0.19 0.008 0.0000* 2.38 0.09 0.0000*
Boron levels (B) 1 0.05 0.05 0.0000* 0.129 0.19 0.0000*
V × B 25 0.03 0.001 0.9643NS 0.41 0.02 0.0132*

Here, SOV = source of variation, df = degree of freedom, SS = sum of squares, MS = mean squares, NS = non-significant, * = significant (p ≤ 0.05).

Effect of boron application on leaf area index of different chickpea genotypes ± SE. Here, DAS = days after sowing.
Fig. 1
Effect of boron application on leaf area index of different chickpea genotypes ± SE. Here, DAS = days after sowing.
Effect of boron application on leaf area duration (day) and crop growth rate (g m−2 day−1) of different chickpea genotypes ± SE. Here, DAS = days after sowing.
Fig. 2
Effect of boron application on leaf area duration (day) and crop growth rate (g m−2 day−1) of different chickpea genotypes ± SE. Here, DAS = days after sowing.
Effect of boron application on net assimilation rate (g m−2 day−1) of different chickpea genotypes ± SE. Here, DAS = days after sowing.
Fig. 3
Effect of boron application on net assimilation rate (g m−2 day−1) of different chickpea genotypes ± SE. Here, DAS = days after sowing.

Genotypes and B application had highly significant effect on plant height and number of nodules per plant. However, interactive effect was significant for plant height and non-significant for number of nodules per plant (Table 1). Boron application improved plant height and number of nodules of all genotypes with varying degree (Table 2). Among ‘desi’ genotypes ‘Bittle-2016’ and ‘Punjab-2008’ resulted in the longest plant height with B application, while the shortest plant height was recorded for genotype ‘TG-1415’ grown without B application and it was statistically at par with genotypes ‘TGK-228’, ‘05A028’, ‘TG-1623’, ‘Thal-2006’, ‘TG-1218’, ‘TG-1513’, ‘Chattan’ and ‘NIAB-2016’ (Table 1). Among ‘kabuli’ genotypes, ‘TGK-1761’ and ‘TGK-228’ resulted in the highest and the lowest plant height, respectively grown with and without B application (Table 1). Likewise, ‘desi’ genotypes ‘TG-1616’, ‘TG-1601’, ‘05A028’, ‘Chattan’, ‘Bittle-2016’ and ‘Punjab-2008’ with B application recorded higher number of nodules per plant compared to the rest of the genotypes and B application treatments (Table 2). However, ‘kabuli’ genotypes ‘TGK-1761’, ‘TGK-1802’ and ‘NOOR-2009’ with or without B application observed higher number of nodules per plant and ‘TGK-228’ grown without B resulted in poor nodulation (Table 2).

Table 2 Effect of boron application on plant height and number of nodules per plant of different chickpea genotypes
Chickpea genotypes Plant height (cm) Number of nodules per plant
Boron levels (kg ha−1)
0.00 1.00 Means 0.00 1.00 Means
TGK-1767 47.55 k-n 55.22 c-f 51.39 C-I 21.33 17.67 19.50 AB
TGK-1802 50.50 g-m 54.23 c-h 52.37 C-H 17.00 17.67 17.33 A-C
NOOR-2009 51.37 d-l 50.93 e-l 51.15 E-I 16.67 16.67 16.67 A-E
TGK-1761 51.63 d-k 57.37 bc 54.50 BC 17.67 16.67 17.17 A-D
TGK-1805 50.78 f-m 52.67 d-i 51.72 C-I 12.67 8.33 10.500 D-F
TGK-228 47.73 k-n 51.67 d-k 49.70 G-I 5.00 15.33 10.17 EF
TG-1430 50.29 h-m 52.91 c-i 51.60 C-I 15.33 15.33 15.33 A-F
Parbat 53.07 c-i 54.80 c-g 53.93 B-E 15.33 17.67 16.50 A-E
TG-1616 51.84 d-k 53.00 c-i 52.42 C-G 13.67 29.00 21.33 A
TG-1620 51.29 d-l 51.28 d-l 51.28 D-I 23.67 16.00 19.83 AB
05A028 46.39 mn 51.27 d-l 48.83 I 19.00 21.67 20.33 AB
TG-1601 51.29 d-l 51.87 d-k 51.58 C-I 17.00 21.00 19.00 AB
TG-1623 48.11 j-n 53.09 c-i 50.60 F-I 13.67 15.00 14.33 B-F
Thal-2006 49.49 i-n 47.89 j-n 48.69 I 15.00 18.33 16.67 A-E
TG-1218 47.11 l-n 50.56 g-m 48.83 I 19.00 15.33 17.17 A-D
TG-1513 48.89 i-n 53.18 c-i 51.03 E-I 11.33 19.33 15.33 A-F
Chattan 48.89 i-n 49.56 i-n 49.22 HI 9.67 20.67 15.17 A-F
BK-2011 52.99 c-i 51.58 d-l 52.28 C-H 6.67 11.33 9.00 F
TG-1500 51.47 d-l 52.62 d-i 52.04 C-H 13.67 19.00 16.33 A-E
NIAB-2016 47.44 k-n 52.33 d-j 49.89 G-I 12.33 17.00 14.67 A-F
GGP-1456 51.11 d-l 61.58 ab 56.34 AB 15.33 18.00 16.67 A-E
TG-1618 51.57 d-l 57.33 bc 54.45 B-D 17.67 15.67 16.67 A-E
TG-1619 51.91 d-k 55.44 cd 53.68 B-F 9.67 12.33 11.00 C-F
Bittle-2016 54.17 c-h 63.60 a 58.88 A 10.00 24.00 17.00 A-D
TG-1415 45.44 n 55.30 c-e 50.37 G-I 19.67 19.00 19.33 AB
Punjab-2008 55.367 c-e 61.33 ab 58.35 A 12.67 26.67 19.67 AB
Means for B 50.29 B 53.95 A 14.64 B 17.87 A
LSD value at 5% B = 0.88, V = 3.18, V × B = 4.50 LSD at 5% B = 1.86, V = 6.71

Means sharing different letters, within a column or row, differ significantly for each trait from each other at P ≤ 5%.

Chickpea genotypes, B application and their interaction had significant effect on number of branches and number of pods per plant (Table 1). Boron application improved the number of branches and number of pods of all genotypes and genotypes behaved differently (Table 3). Among ‘desi’ genotypes ‘Punjab-2008’, ‘Chattan’, ‘TG-1500’, ‘NIAB-2016’ and ‘GGP-1456’ recorded higher number of branches per plant compared with B application compared to the rest of the genotypes grown with or without B. However, all ‘kabuli’ genotypes recorded similar number of branches per plant with or without B application (Table 3). Moreover, ‘desi’ genotypes ‘Punjab-2008’ and ‘Bittle-2016’ with B application recorded higher number of pods per plant, while genotypes ‘TG-1601’, ‘TG-1623’ and ‘05A028’ recorded the lowest number of pods per plant with B application (Table 3).

Table 3 Effect of boron application on number of branches and number of pods per plant of different chickpea genotypes
Chickpea genotypes Number of branches per plant Number of pods per plant
Boron levels (kg ha−1)
0.00 1.00 Means 0.00 1.00 Means
TGK-1767 4.45 f-l 4.33 g-l 4.39 F 41.00 f-j 45.33 c-g 43.167 E-H
TGK-1802 3.67 j-l 4.22 g-l 3.94 EF 38.67 h-k 44.44 d-g 41.555 GH
NOOR-2009 5.55 c-i 4.11 g-l 4.83 B-F 43.89 d-h 45.77 c-g 44.833 B-G
TGK-1761 4.22 g-l 3.56 kl 3.89 EF 46.22 c-f 44.67 d-g 45.445 B-F
TGK-1805 5.00 c-l 4.00 g-l 4.50 C-F 35.44 k 44.99 d-g 40.217 H
TGK-228 3.67 j-l 5.44 c-j 4.55 C-F 42.56 e-i 44.69 d-g 43.623 D-H
TG-1430 4.67 d-l 4.00 g-l 4.33 C-F 48.22 cd 44.24 d-g 46.233 B-E
Parbat 4.45 f-l 3.89 h-l 4.19 C-F 46.67 c-e 46.55 c-e 46.612 B-E
TG-1616 4.22 g-l 4.55 e-l 4.39 C-F 43.78 d-h 50.56 bc 47.167 A-D
TG-1620 3.67 j-l 4.33 g-l 4.00 D-F 47.33 c-e 48.67 b-d 48.00 A-C
05A028 3.78 i-l 4.67 d-l 4.22 C-F 40.67 g-k 48.00 cd 44.33 C-G
TG-1601 3.22 l 4.11 g-l 3.66 F 36.33 jk 47.33 c-e 41.83 F-H
TG-1623 4.45 f-l 5.22 c-k 4.83 B-F 38.67 h-k 48.44 cd 43.55 D-H
Thal-2006 3.78 i-l 6.22 a-f 5.00 B-E 41.00 f-j 44.67 d-g 42.83 E-H
TG-1218 4.22 g-l 5.66 c-h 4.94 B-F 47.00 c-e 48.00 cd 48.00 A-C
TG-1513 3.56 kl 4.66 d-l 4.11 D-F 45.78 c-g 47.33 c-e 44.33 C-G
Chattan 4.22 g-l 6.67 a-c 5.44 A-C 45.33 c-g 44.24 d-g 47.00 A-D
BK-2011 4.89 c-l 4.55 e-l 4.55 C-F 48.55 cd 48.22 cd 48.39 AB
TG-1500 4.56 e-l 6.33 a-e 4.39 C-F 48.67 b-d 47.11 c-e 47.89 A-C
NIAB-2016 4.11 g-l 6.44 a-d 5.28 A-D 46.67 c-e 48.33 cd 47.50 A-C
GGP-1456 4.33 g-l 7.56 ab 5.94 AB 45.67 c-g 48.33 cd 47.00 A-D
TG-1618 3.55 kl 4.89 c-l 4.22 C-F 42.56 e-i 48.33 cd 45.44 B-F
TG-1619 3.56 kl 6.22 a-f 4.89 B-F 48.33 cd 47.78 c-e 47.22 A-D
Bittle-2016 4.44 f-l 5.44 c-j 4.94 B-F 37.22 i-k 54.00 ab 48.05 A-C
TG-1415 4.00 g-l 5.78 b-g 4.89 B-F 43.67 d-h 50.67 bc 47.17 A-D
Punjab-2008 4.55 e-l 7.78 a 6.33 A 47.00 c-e 57.223 a 50.50 A
Means for B 4.18 B 5.18 A 43.73 B 47.78 A
LSD at 5% B = 0.09, V = 0.34, V × B = 0.48 LSD at 5% B = 1.06, V = 3.81, V × B = 5.39

Means sharing different letters, within a column or row, differ significantly for each trait from each other at P ≤ 5%.

Chickpea genotypes, B application and their interaction had significant effect on 1000-grain weight and grain yield of chickpea except for non-significant of interaction on grain yield (Table 1). Boron application improved 1000-grain weight and grain yield of all genotypes with varying degree (Table 4). Among ‘desi’ genotype ‘Punjab-2008’ and ‘kabuli’ genotype ‘NOOR-2009’ recorded higher 1000-grain weight grown with B application (Table 4). Moreover, ‘desi’ genotypes ‘Bittle-2016’ and ‘TG-1619’ with B application produced higher yield than all other genotypes, while ‘BK-2011’ and ‘TG-1620’ produced the lowest yield without B application (Table 4). Among ‘kabuli’ genotypes, ‘NOOR-2009’ recorded higher grain yield with B application (Table 4). Among ‘desi’ genotypes, ‘Punjanb-2008’ with B application recorded the highest grain yield and it was at par with ‘Bittle-2016’ and ‘TG-1619’, whereas ‘NOOR-2009’ ‘kabuli’ genotype with B application recorded higher grain yield compared to the rest of the ‘kabuli’ genotypes (Table 4).

Table 4 Effect of boron application on 1000-grain weight and grain yield of different chickpea genotypes
Chickpea genotypes 1000-grain weight (g) Grain yield (t ha−1)
Boron (kg ha−1)
0.00 1.00 Means 0.00 1.00 Means
TGK-1767 428.47 op 445.00 e-k 436.73 C-H 2.41 2.77 2.59 D-G
TGK-1802 418.77 tu 438.03 mn 428.40 L 2.43 2.73 2.58 D-G
NOOR-2009 439.90 k-m 458.50 b 449.20 A 2.78 3.03 2.90 AB
TGK-1761 420.90 r-u 444.97 e-k 432.93 H-K 2.34 2.63 2.49 FG
TGK-1805 418.53 tu 446.30 d-j 432.42 I-K 2.24 2.67 2.45 G
TGK-228 428.21 op 446.27 d-j 437.24 C-F 2.27 2.70 2.53 E-G
TG-1430 418.60 tu 447.97 d-h 433.28 G-K 2.68 2.97 2.82 B-D
Parbat 427.30 o-q 447.03 d-j 437.17 C-G 2.33 2.93 2.63 C-G
TG-1616 428.23 op 448.73 d-f 438.48 CD 2.34 2.90 2.62 C-G
TG-1620 421.00 r-u 442.67 h-m 431.83 J-L 2.50 2.87 2.68 B-G
05A028 425.93p-r 444.00 f-l 434.97 C-J 2.72 2.90 2.81 B-D
TG-1601 427.17 o-q 450.07 c-e 438.62 C 2.62 2.80 2.71 B-G
TG-1623 425.63 p-r 443.63 f-l 434.63 D-J 2.69 2.77 2.73 B-F
Thal-2006 427.23 o-q 443.63 f-l 435.43 C-J 2.41 2.83 2.62 C-G
TG-1218 427.07 pq 442.03 i-m 434.55 E-J 2.50 2.90 2.70 B-G
TG-1513 420.90 r-u 446.03 d-j 433.47 F-K 2.67 2.97 2.82 B-D
Chattan 425.30 p-r 443.00 g-m 434.15 E-K 2.31 2.93 2.62 C-G
BK-2011 419.20 s-u 444.97 e-k 432.08 J-L 2.43 2.81 2.62 C-G
TG-1500 418.93 tu 441.70 j-m 430.32 KL 2.57 2.88 2.72 B-F
NIAB-2016 416.93 u 450.70 cd 433.82 F-K 2.37 2.82 2.67 B-G
GGP-1456 422.17 q-u 444.80 e-l 433.48 F-K 2.33 2.90 2.58 D-G
TG-1618 423.60 p-t 446.67 d-j 435.13 C-J 2.63 2.90 2.77 B-E
TG-1619 427.50 o-q 448.33 d-g 437.92 C-E 2.90 2.87 2.88 BC
Bittle-2016 432.67 no 455.40 bc 444.03 B 2.83 3.00 2.92 AB
TG-1415 424.57 p-s 447.43 d-i 436.00 C-I 2.73 2.90 2.82 B-D
Punjab-2008 439.33 lm 466.03 a 452.68 A 3.07 3.27 3.17 A
Means for B 425.16 B 447.07 A 2.54 B 2.87 A
LSD value at 5% B = 1.08, V = 3.90, V × B = 5.52 LSD at 5% V = 0.27, B = 0.07

Means sharing different letters, within a column or row, differ significantly for each trait from each other at P ≤ 5%.

Chickpea genotypes and B application had significant effect on biological yield and harvest index, while their interaction had non-significant effect (Table 1). Boron application improved biological yield of all genotypes (Table 5). Among ‘desi’ genotypes ‘Punjab-2008’ observed higher biological yield than all other genotypes (Table 5). Similarly, among ‘kabuli’ genotypes, ‘NOOR-2009’ recorded higher biological yield, whereas ‘TGK-1767’ produced the lowest biological yield (Table 5). The B application at 1 kg ha−1 resulted in higher biological yield compared with no B application. Regarding interactions, ‘Punjab-2008’ with B application recorded the highest biological yield among ‘desi’ genotypes, while ‘NOOR-2009’ had the highest biological yield with B application among ‘kabuli’ genotypes (Table 5). The lowest biological yield was recorded for ‘Parbat’ among ‘desi’ genotypes, ‘TGK-1767’ produced the lowest biological yield among ‘kabuli’ genotypes (Table 5). Among desi genotypes, ‘TG-1601’ and ‘05A028’ observed higher harvest index, whereas ‘TGK-1767’ recorded highest harvest index among ‘kabuli’ genotypes (Table 5).

Table 5 Effect of boron application on biological yield and harvest index of different chickpea genotypes.
Chickpea genotypes Biological yield (t ha−1) Harvest index (%)
Boron levels (kg ha−1)
0.00 1.00 Means 0.00 1.00 Means
TGK-1767 6.85 7.80 7.33 E-H 35.21 35.45 35.33
TGK-1802 6.88 7.76 7.32 E-H 35.20 35.16 35.18
NOOR-2009 7.59 8.58 8.09 B 36.66 35.33 35.99
TGK-1761 6.79 7.51 7.15 GH 34.30 35.03 34.67
TGK-1805 6.50 7.63 7.07 H 34.36 34.96 34.66
TGK-228 6.81 7.74 7.27 F-H 34.38 34.90 34.64
TG-1430 7.38 8.20 7.79 B-E 36.23 36.15 36.19
Parbat 6.84 8.14 7.49 D-H 33.69 36.02 34.85
TG-1616 6.70 8.07 7.39 E-H 34.83 35.93 35.38
TG-1620 7.02 8.00 7.51 D-H 35.54 35.81 35.67
05A028 7.46 8.07 7.76 B-F 36.2 35.93 36.18
TG-1601 7.26 7.87 7.56 C-H 35.84 35.57 35.71
TG-1623 7.65 7.80 7.73 B-F 35.06 35.44 35.25
Thal-2006 7.09 7.90 7.49 D-H 33.95 35.86 34.90
TG-1218 7.26 8.06 7.66 B-G 34.39 35.94 35.16
TG-1513 7.60 8.24 7.92 B-D 35.04 35.99 35.52
Chattan 6.88 8.13 7.50 D-H 33.38 36.10 34.79
BK-2011 7.14 7.89 7.51 D-H 34.04 35.57 34.81
TG-1500 7.41 8.02 7.72 B-F 34.62 35.83 35.23
NIAB-2016 7.01 8.22 7.62 B-G 33.76 36.17 34.96
GGP-1456 6.93 7.90 7.42 D-H 33.58 35.63 34.61
TG-1618 7.55 8.07 7.81 B-E 34.83 35.93 35.38
TG-1619 8.10 8.03 8.07 BC 35.80 35.66 35.73
Bittle-2016 7.93 8.18 8.05 BC 35.73 36.68 36.21
TG-1415 7.74 8.07 7.90 B-D 35.30 35.93 35.62
Punjab-2008 8.41 9.03 8.72 A 36.46 36.18 36.32
Means for B 7.26 B 8.04 A 35.74 A 34.95 B
LSD at 5% B = 0.14, V = 0.52 LSD at 5% B = 0.37

Means sharing different letters, within a column or row, differ significantly for each trait from each other at P ≤ 5%.

Chickpea genotypes, B application and their interaction had significant effect on grains B concentration (Table 1). Boron application improved grain B concentrations of all genotypes and genotypes significantly differed in this regard (Table 5). Among ‘desi’ genotypes, ‘TG-1500’, ‘Chattan’, ‘05A028’, ‘TG-1620’ and ‘NIAB-2016’ recorded higher grain B concentration (Table 6). Among ‘kabuli’ genotypes, ‘TGK-1767’ recorded the highest grain B concentration (Table 6). Regarding interaction, ‘TG-1500’, ‘BK-2011’ and ‘NIAB-2016’ with B application recorded the highest grain B concentration among ‘desi’ genotypes, while ‘TGK-1767’ and ‘TGK-228’ with B supplementation had higher grain B contents among all ‘kabuli’ genotypes (Table 6).

Table 6 Effect of boron application on grains boron concentration in different chickpea genotypes.
Chickpea genotypes Grains boron concentrations (mg kg1)
Boron (kg ha1)
0.00 1.00 Means
TGK-1767 2.81 v 57.62 d-g 30.22 G-J
TGK-1802 8.60 q-v 50.13 g-i 29.37 H-J
NOOR-2009 7.96 r-v 38.57 j 23.27 K
TGK-1761 5.18 uv 55.05 e-h 30.11 G-J
TGK-1805 18.45 k-o 55.91 d-h 37.18 C-E
TGK-228 19.95 k-n 60.83 b-e 40.39 B-E
TG-1430 7.96 r-v 48.63 hi 30.44 G-J
Parbat 12.03 n-u 48.84 hi 35.04 E-H
TG-1616 14.81 n-t 55.27 e-h 36.86 D-F
TG-1620 9.67 p-v 64.04 a-d 35.25 E-G
05A028 7.75 s-v 62.76 a-e 37.61 C-E
TG-1601 16.52 l-q 58.69 c-f 27.97 I-K
TG-1623 5.61 uv 50.34 g-i 28.94 I-K
Thal-2006 7.53 s-v 50.34 g-i 25.40 JK
TG-1218 7.32 t-v 43.49 ij 34.93 E-H
TG-1513 24.87 k 44.99 ij 42.64 A-D
Chattan 24.66 kl 60.62 b-e 42.74 A-C
BK-2011 18.02 k-o 67.47 ab 42.75 A-C
TG-1500 24.66 kl 70.89 a 47.77 A
NIAB-2016 23.37 k-m 66.40 a-c 44.88 AB
GGP-1456 15.67 m-s 58.26 c-g 36.96 C-F
TG-1618 16.10 m-r 59.97 b-e 38.03 C-E
TG-1619 11.39 o-u 63.83 a-d 37.61 C-E
Bittle-2016 11.39 o-u 51.20 f-i 31.29 F-I
TG-1415 15.31 m-t 44.99 ij 30.15 G-J
Punjab-2008 17.59 k-p 55.48 e-h 36.54 EF
Means of B 13.66 B 55.56 A
LSD at 5% B = 1.60 , V=5.79 , V × B = 8.18

Means sharing different letters, within a column or row, differ significantly for each trait from each other at P ≤ 5%.

4

4 Discussion

The results the current study supported our hypothesis that B application significantly improved growth, nodulation, yield related traits and grain B concentration (Figs. 1–3, Tables 1–6). All genotypes responded differently under B availability and genetic makeup is thought to be responsible for this response. Equal amount of B was applied to each genotype; however, their response varied to a great extent. Ceyhan et al. (2007) unveiled that chickpea genotypes had varying response to supplementation because of their divergent genetic makeup. More B application improved grain B concentration of all tested genotypes (Table 6).

Boron is an essential element and undoubtedly plays structural role in cell walls and the maintenance of plasma membrane functions, sugar transport, carbon-fixation, lignification, ribose nucleic acid metabolism and indole acetic acid metabolism (Flores et al., 2017). Application of B considerably enhanced LAI, LAD, CGR and NAR which boosted the productivity of chickpea (Figs. 1–3). Leaf area index is important factor of growth rate and yield which is an alternative for the measurement of photosynthesis. Boron was applied at sowing, so it was expected to influence growth traits, especially LAI, LAD and CGR (Figs. 1–3). Boron application before vegetative stage resulted in higher LAI through improved LAD (Al-Amery et al., 2011). With respect to ‘desi’ genotypes, ‘Punjab-2008’ recorded higher LAI, LAD and CGR, whereas in ‘kabuli’ genotypes ‘NOOR-2009’ had higher values of these traits (Figs. 1–3). Leaf area is considered as main part of photosynthesis and directly affects photosynthesis rate. According to Yamori et al. (2016), photosynthesis rate directly depends on chlorophyll content and leaf area index, which ultimately enhanced grain yield and dry matter production. Chickpea plants observed reduction in LAI, LAD and dry weight under no B application which resulted in lower photosynthetic rate and reduced production (Figs. 1–3). Under drought conditions, photosynthesis rate and water status is improved by B application (Lu et al., 2014).

Boron application significantly improved plant height, nodulation, number of grains per plant and 1000-grain weight leading to higher grain yield. Bayrak et al. (2005) reported that B application in B‐deficient soils has significant effect on number of pods per plant in chickpea. Sarker et al. (2002) reported that B application 1000-grain weight in soybean (Glycine max L.). Oosterhuis and Zhao (2001) stated that B is very important for germination and development of pollen tube, seed maturity, richness of floret, anther growth and plasma membrane encouragement. Nutrient and water availability during vegetative stage helps in biomass accumulation. Results of this study reported that ‘desi’ genotypes, especially ‘Punjab-2008’ had higher plant height, branches, and pods per plant under B application compared to other genotypes which might be due to more nodulation (Tables 2–3).

Boron application enable plants to produce a greater number of pods, nodules, and quality grains because it plays active role in assimilated partitioning and transport (Zohaib et al., 2018). Better movement of assimilates from source to sink, improved pollen fertility and grains development are the major role of B in plants. Therefore, chickpea yield-related traits were improved under B application. Application of B improved number of nodules (18%), branches (19%), number of pods (8.5%) and 1000 grain weight (5%) as compared to no B application (Tables 2–4). Due to increase in all yield-related traits under B application, chickpea grain yield and biological yield were increased by 11.5% and 10% respectively. Boron application also improved grain B concentration in plants by ∼75% which fulfil the requirement of B in grains and mitigate the malnutrition problem (Table 6). According to Hussain et al. (2020), biofortification of B economically increased gains/pod and 1000-grain weight in chickpea.

When assimilate move easily, plants produce higher net returns because of their utilization. Ceyhan et al. (2008) revealed that soil application of boron at 7.5 kg B ha−1 increased grain yield and plant height not only in 1st year but the positive effect was also visible on next year. Boron application improved total dry matter by three times in B-deficient plants than in B-sufficient plants (Asad et al., 2003). Soil application of B along with Bacillus sp. MN54 inoculation substantially augmented number of pods plant−1 (38%), nodulation (81%) and grain yield (47%) compared with control treatment (Mehboob et al., 2021).

All crops and varieties may vary in their ability to uptake B from soils. This variation is primarily directed by their genetic structure, although environmental issues and plant morphology play a certain role in this variation. In this study, ‘Punjab-2008’ ‘desi’ genotypes and ‘NOOR-2009’ ‘kabuli’ genotype showed better response to B application. These genotypes recorded higher productivity due to notable expansion in nodulation, number of pods and 1000-grain weight. Observing the amount of B in eatable portions of cereals and pulses both by B and no B application may be helpful for the screening of B enriched varieties. Biofortification is an only option today to reduce the effect of malnutrition by entering the essential minerals to our diet.

5

5 Conclusions

Chickpea genotypes (desi and kabuli) had different response to soil application of B. From 20 ‘desi’ genotypes, ‘Punjab-2008’ recorded higher nodulation, pods per plant, 1000-grain weight, grain yield and B-grain concentration with B application. In case ‘kabuli’ genotypes, ‘NOOR-2009’ observed higher nodulation, 1000-grain weight grain and biological yields with B application. In conclusion, desi genotype ‘Punjab-2008’ and ‘kabuli’ genotype ‘NOOR-2009’ are better option to increase chickpea growth, nodules population, productivity, and grain concentration under B application.

Acknowledgement

The authors extend their appreciation to the Researchers supporting project number (RSP-2021/247) King Saud University, Riyadh, Saudi Arabia.

Declaration of Competing Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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