Research Article

Performance of Different Wheat Cultivars in Semi-arid Ecological Conditions

Zarghoona1, Khilwat Afridi2, Ruby Wali Khan1, Haseeba1, Rahmat Elahi1, Nadia1, Kashmala Jabbar1, Guleena Khan1, Ikramullah Khan1, Haleema Bibi2, Abdur Rauf1*

1Garden Campus, Abdul Wali Khan University, Mardan, Pakistan; 2Cereal Crop Research Institute Pirsabak, Nowshera, Khyber Pakhtunkhwa, Pakistan.

Abstract | A field trial of 49 wheat genotypes was performed in an alpha lattice design to evaluate the phenological and morphological traits. The data analysis revealed considerable variations among genotypes for traits like days to heading (81–97), days to maturity (152–157), plant height (80.7–97 cm), flag leaf area (16.2–31.7 cm²), peduncle length (23.0–33.3 cm), tillers per square meter (116–440), spike length (8.0–12.4 cm), spikelet’s per spike (14.8–20.8), thousand-grain weight (27.0–49.2 gm), biological yield (5375–13250 Kg/ha), grain yield (1375–5290 Kg/ha), and harvest index (23.5–53.1%). The genotypes, PR-156 had the earliest maturity, Nia Zarkhaize with the highest tillers per square meter, while PR-153 recorded the highest 1000-grain weight. Pirsabak-15 and Pirsabak-23 had the highest grain and biological yields, respectively. Highly significant positive correlations, such as days to heading with maturity (rP = 0.89**), tillers and grain yield with biological yield (rP = 0.35 ** & rP = 0.87**), and harvest index with 1000-grain weight (rG = 0.50**), highlighted the coordinated genetic control. These correlations indicate that the selection could simultaneously enhance the given traits in breeding programs. On the other hand, the genotype Pirsabak-15 is a candidate line for grain yield increase and may be considered for future wheat breeding programs.


Received | April 29, 2025; Accepted | June 24, 2025; Published | June 26, 2025

*Correspondence | Abdur Rauf, Garden Campus, Abdul Wali Khan University, Mardan, Pakistan; Email: [email protected]; [email protected]

Citation | Zarghoona, K. Afridi, R.W. Khan, Haseeba, R. Elahi, Nadia, K. Jabbar, G. Khan, I. Khan, H. Bibi, A. Rauf. 2025. Performance of different wheat cultivars in semi-arid ecological conditions. Pakistan Journal of Weed Science Research, 31(2): 132-150.

DOI | https://dx.doi.org/10.17582/journal.PJWSR/2025/31.2.132.150

Keywords | Bread wheat, Cultivars, Heritability, Genetic advance, Phenotypic Coefficient of variation, Genotypic Coefficient of variation

Copyright: 2025 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).



Introduction

Wheat (Triticum aestivum L.), a member of the family Poaceae, is a staple grain crop grown worldwide, primarily for human consumption (Ahmad et al., 2020). As a self-pollinated, long-day crop, wheat ranks first among cereal crops in terms of cultivation and grain yield in regions like Uruguay, Australia, Argentina, Syria, and Morocco (Arzadun et al., 2006). Globally, wheat is cultivated from sea level to altitudes exceeding 3000 meters.

The wheat cropping system is pivotal to Pakistan’s agriculture-dependent economy. It ensures food security for the rapidly growing population and contributes significantly to foreign exchange (Amin et al., 2017). The main wheat-growing regions are in the Indus plains across Pakistan, approximately 900 meters above sea level (PARC, 2009), while Pakistan ranks 9th in wheat cultivation area and 7th in production globally (MINFAL, 2022-23). Deploying high-yield, rust-resistant spring wheat cultivars is crucial to meet the country’s increasing food demands (Muhammad et al., 2017; Sadiq et al., 2025). Selection for yield components, aided by traits with high heritability and genetic advancement, is essential for enhancing yield potential (Balkan, 2018). However, negative correlations among yield attributes can hinder breeding programs, emphasizing the importance of breaking unfavorable linkages (Abdulhamed et al., 2021). The development of new spring wheat cultivars has led to significant increases worldwide (Rauf et al., 2023). Farmers favor cultivars with stable performance across diverse environments (Hancock, 2004).

Genetic diversity is vital for developing novel genotypes and can be measured through morphological traits, molecular markers, or pedigree analysis (Habash et al., 2009; Rauf et al., 2023). Traits like plant height, grain number, and spikes per unit area exhibit significant genetic variation, aiding selection for higher yields. Genotypic associations among yield-contributing traits play a crucial role in determining their influence on grain production (Salman et al., 2014; Rauf et al., 2023). The genetic architecture of yield-related traits is fundamental to wheat improvement. Correlation studies between quantitative traits and their direct and indirect effects on grain yield are indispensable for breeding programs (Khan et al., 2010; Sadiq et al., 2025). Wheat breeders focus on developing resilient cultivars with enhanced grain yield to meet the needs of the growing population (Mangova and Rachovska, 2004).

Bread wheat is highly adaptable, thriving in diverse climatic conditions. Climate change poses significant challenges to Pakistan’s agriculture, with rising greenhouse gas emissions exacerbating temperature increases and affecting crop growth. Developing wheat cultivars that can withstand adverse environmental conditions is vital. The interaction between genotype and environment (GEI) plays a key role in determining the stability and performance of wheat genotypes across diverse conditions (Sadiq et al., 2025; Khan et al., 2023). Multi-environment trials assess genotype adaptability and help identify superior cultivars (Piepho et al., 2012). Soil, climate, and management practices are critical factors influencing wheat genotype performance. Temperature changes, particularly terminal heat stress above 22–24 °C, adversely affect wheat grain yield. Heat-tolerant cultivars with broad adaptability are essential for increasing productivity (Shafi et al., 2013; Khan et al., 2023).

Correlation coefficients help determine the relationship between grain yield and yield components. Days to maturity and thousand-grain weight are highly positively correlated with grain yield (Gelalcha and Hanchinal, 2013). The path coefficient analysis would go deeper into yield components’ direct and indirect effects (Del-Moral et al., 2003). Such analyses guide breeders to identify traits critical for yield improvement. Genetic heritability and variability provide essential information for crop improvement. Traits with high heritability and genetic advancement are crucial for selecting superior genotypes (Ibrahim et al., 2020). Mutagenic trait inheritance, assessed through heritability, supports efficient breeding strategies (Bhargava et al., 2003). Global wheat production must rise significantly to meet the increasing demand driven by population growth, necessitating the development of robust cultivars (FAO, 2018).

Greater genetic diversity in base populations increases the likelihood of developing desirable plant types. This study analyzed 49 wheat genotypes to estimate genetic diversity, heritability, and genetic gain for traits related to productivity and quality, providing insights for future crop improvement efforts. The current project was designed to identify the high-yielding wheat varieties with genetic diversity, adaptability, and yield potentials suitable for the semi-arid to sub-humid agroecological conditions of Peshawar Valley, KP.

Materials and Methods

Experimental Materials and Resources

A total of 49 wheat genotypes, which include 11 advanced lines and 38 potential cultivars, were cultivated in two repetitions in a seven-by-seven Alpha lattice square configuration at the Cereal Crop Research Institute (CCRI), Pirsabak Nowshera, Pakistan (Table 1). The agronomic cultural methods were used in the field trial, where four rows, two meters long and 25 centimeters apart, were used for sowing seeds.

These 49 wheat lines were analyzed for different parameters, including days to heading, days to maturity, plant height, flag leaf area (width × length × 0.75), peduncle length, tiller per square meter (Total Number of Tillers/Number of Rows× R-R space × Row length), Spike Length, Spikelets spike-1, Thousand-grain weight, Biological yield, Grain yield, Harvest Index (Grain yield/Biological Yield×100).

 

Table 1: Details of 49 different wheat genotypes used in the field trial.

S.N.

Genotypes

S.N.

Genotypes

S.N.

Genotypes

1

PR.138

18

Pirsabak-19

35

Zincol-16

2

PR.139

19

Gulzar-19

36

Pakistan-13

3

PR.141

20

Abaseen-21

37

MA-20

4

PR.142

21

Zarghoona-21

38

Akbar-19

5

PR.146

22

Pirsabak-21

39

Subhani-21

6

PR.147

23

Taskeen-22

40

M.H-21

7

PR.148

24

Fahim-19

41

Dilkash-21

8

PR.149

25

Kohat-17

42

V-19347

9

PR.150

26

Kt-22

43

Ghazi19

10

PR.151

27

Swabi-1

44

Nawab-21

11

PR.152

28

NIFA Lubna

45

NIA Shaheen

12

Pirsabak-13

29

S.N-005

46

NIA Sunhari

13

Shahkar-13

30

TRB-2-103

47

NIA Zarkhaize

14

pirsabak-15

31

Wafaq-23

48

Fakhar-e-Bakkar

15

paseena-17

32

NAKC Super

49

Bakkar star

16

wadan-17

33

Makaf-19

17

Khaista-17

34

Borlaug-16

 

Statistical Analysis

The variance data were analyzed using Steel and Torri (1980) for the Alpha lattice design (Table 2). The least significant difference (LSD) was used to differentiate between means. The computer software MSTAT-C and TUANSTAT were utilized to analyze variance (ANOVA) and correlation among various traits.

 

Table 2: Anova for Alpha Lattice Design.

Source of Variations

DF

SS

Envi

e-1

SSe

Geno (unadjusted)

g-1

SSg

Blocks (within replications)

rs-r

SSb

Geno (Adjusted)

g-1

SSg

RCB

(g-1) b(r-1)

SSrb

Geno x Envi.

(g-1)(e-1)

SSge

Intra Block Error

e(g-1)(r-1)

Sse

Total

egr-1

SST

 

Correlation analysis

Genotypic and phenotypic correlations for various morphological, physiological, and biochemical traits were computed for both genotypic and phenotypic correlations using TNAUSTAT software (Manivannan, 2014).

Results and Discussion

We have analyzed several variables, including days to heading, days to maturity, plant height, flag leaf area, peduncle length, tillers meter-2, spikelets per spike, spike length, thousand-grain weight, biological yield, grain yield, and harvest index. This was designed to estimate genetic diversity, heritability, genetic advance, and correlation analysis of 49 genotypes of bread wheat related to the important above-mentioned traits. The statistical analyses of the mean square, mean values, LSD, heritability, genetic advance, genotypic, and phenotypic correlation values are shown (Tables 3, 4, 5, 6, 7 and 8).

Days to heading

Analysis of variance revealed a significant difference in the heading (P≤ 0.01) among the tested genotypes. The coefficient variation for days to heading was 0.70%. The mean heading interval was 117.0 days for the 49-genotype set, with a range from 81 to 97 days (Table 5). The maximum (97) and minimum (81) days heading were reported for GULZAR-19 and PIRSABAK-21, respectively (Figure 1 and Table 5). The three days were the least significant change (LDS) of 5% for the direction. The heritability estimate of heading was 0.98, while genetic advance was 6.12 (Table 7). Moderate genetic advancement combined with a high heritability is shown for heading (Table 7).

Results for heading were also supported by Chauhan et al. (2022), who found highly significant differences for a set of 40 genotypes evaluated in a randomized complete block design in 2021. Likewise, Iqbal et al. (2017) evaluated 16 wheat genotypes and found a CV of 0.98% for heading. Gerema et al. (2020) evaluated 180 genotypes during 2017-18, where they noted a CV of 1.60% for days to heading. Tefera (2022) also supports the current mean range for maturity interval, which varied between 48-80 days for 81 genotypes evaluated. Early studies by Dabi et al. (2017) found a high heritability of 86.4% with very low genetic gain

 

Table 3: Mean squares for days to heading, days to maturity, plant height, flag leaf area, peduncle length, and tillers per meter square at CCRI during 2022-23.

SOV

DF

DH

DM

PH

FLA

PL

TM

REPS

1

2.78**

0.26

4.50*

2.30

0.65

4.08

Geno.(unadjusted)

48

39.36**

2.91**

37.99**

15.92**

9.14**

15379.90**

Blocks within Reps/ Block

14

9.60

0.49

10.57

2.09

0.56

5.54

Geno. (adjusted)

48

38.87**

2.99**

37.83**

15.45**

9.14**

15162.31**

RCB

48

3.14

1.42

3.95

1.59

0.65

4.08

Intra block error

42

0.39

1.46

1.00

1.12

0.56

2.82

CV

--

0.70

0.78

1.13

4.60

1.50

3.39

 

**, * significant at 1% and 5% respectively.

 

Table 4: Mean squares for spike length, Spikelets spike-1, 1000 grain weight, grain yield, biological yield, and harvest index at CCRI during 2022-23.

 SOV

 Df

SL

SPS

TGW

GY

BY

HI

REPS

1

0.84*

0.02

0.16

1493979.59**

5739.795918

0.826530612

Geno (unadjusted)

48

1.88**

4.04**

40.89**

924014.58**

6060958.759**

52.43275248**

Blocks within Reps/ Block

14

1.07

0.64

0.22

1330706.49

7789.723032

1.121720117

Geno (adjusted)

48

1.89**

4.07**

39.31**

888121.17**

5540442.471**

49.81130822**

RCB

48

0.43

0.81

0.16

456981.68

5739.795918

0.826530612

Intra block error

42

0.14

0.71

0.11

78695.94

3963.19242

0.570699708

CV

98

3.75

4.67

0.85

7.63

0.64

2.08

 

for heading and supported these findings regarding heritability. These differences in results about genetic gain may be related to the genetic materials used in the experiments.

Days to maturity

Analysis of variance across maturity revealed highly significant differences between the genotypes (P≤ 0.01) (Table 3). The coefficient of variation for days to maturity was 2.41%. The general mean for the maturity period among the 64 genotypes in the collection was 154 days, while the minimum and maximum ranges were from 152 to 157 days. The shortest period of 152 days was obtained in PR-156, and the longest period of 157 days was obtained in SWABI-1 (Table 3). The LSD 5% took two days for maturity. Mature genes had a heritability value of 0.34 and genetic advances of 0.74. Low genetic progress was observed for maturity, and moderate heritability was fixed (Table 5).

 

Table 5: Means performances of wheat advanced lines for days to heading, days to maturity, plant height, flag leaf area, peduncle length, and tillers per square meter at CCRI during 2022-23.

Varieties

Days to heading

Days to maturity

Plant height

(cm)

Flag leaf area(cm2)

Peduncle length(cm)

Tiller meter

(m-2)

PR-49

84

156

83.8

23.3

32.7

116.0

PR-152

94

155

92.5

19.9

27.3

240.0

PR-153

93

153

92.5

21.5

27.1

260.0

PR-154

87

156

87.0

20.8

29.3

360.0

PR-155

94

153

93.3

21.9

28.1

400.0

PR-156

86

152

85.3

21.0

29.0

200.0

PR-157

94

155

89.0

23.1

30.0

160.0

PR-158

90

154

89.5

25.7

31.0

230.0

PIRSABAK-13

86

154

86.2

20.4

30.0

200.1

SHAHKAR-13

91

155

91.3

16.2

26.3

300.0

PIRSABAK-15

92

156

92.0

18.9

30.0

400.1

PASEENA-17

81

153

81.3

25.2

29.7

360.0

WADAN-17

97

154

96.5

25.2

33.3

140.1

KHAISTA-17

89

154

89.3

26.0

27.7

200.0

PIRSABA-19

83

156

83.0

22.5

31.3

204.1

GULZAR-19

97

156

97.0

25.0

30.3

136.0

ABASEEN-21

90

156

90.0

22.4

27.7

200.1

ZARGHOON-21

94

155

93.8

26.3

33.3

300.0

PIRSABAK-21

81

153

80.7

31.7

31.0

240.1

TASKEEN-22

86

153

86.3

26.0

32.3

160.0

PIRSABAK-23

90

154

90.0

23.4

32.3

300.1

KHYBER-23

90

154

90.0

21.7

32.0

156.0

ABDUL BARI-24

89

155

89.2

25.0

29.0

160.1

FAHIM-19

92

156

91.8

20.4

30.3

280.0

KT-17

90

155

89.0

22.1

32.4

280.1

TANDA-23

94

155

93.8

24.6

32.3

300.0

SWABI-1

84

157

84.2

28.9

29.3

180.1

NAURANG-23

86

154

86.3

20.7

32.7

372.0

TARNAB RAHBER

86

153

84.7

23.8

32.3

128.1

TARNAB GANAM

93

155

93.0

23.1

29.7

176.0

NIFA LALMA

81

152

80.7

23.5

32.8

200.1

NIFA NIJAT

93

154

92.5

24.0

30.7

180.0

FAHR E NIFA

95

155

94.5

19.8

28.7

400.1

WAFAQ-23

87

156

88.3

19.6

30.3

240.0

NARC SUPER

94

155

93.7

21.1

31.7

276.1

MARKAZ-19

84

154

83.5

23.0

31.7

180.0

BORLUG-16

88

153

87.7

27.7

31.3

200.1

ZINCOL16

89

153

89.3

24.5

32.8

300.0

MA-20

89

155

88.5

22.7

28.3

420.1

AKBAR-19

81

156

81.0

19.7

30.0

200.0

DILKASH-21

86

153

85.7

25.2

27.7

350.1

UROOJ-2022

88

155

88.3

27.5

27.3

220.0

GHAZI-19

88

154

86.5

24.5

32.7

300.1

NAWAB-21

83

154

82.5

22.1

29.7

260.0

NIA SHAHEEN

92

152

92.2

21.8

31.0

190.1

NIA SUNHERI

88

155

88.3

21.5

31.0

300.0

NIA ZARKHAIZE

81

154

81.2

20.3

23.0

420.1

F.BAKKAR

90

156

90.0

20.6

30.4

440.0

BAKKAR STAR

95

156

95.0

22.2

32.4

196.1

GM

88.8

154.4

88.6

23.0

30.3

253.3

LSD

1.25

2.44

2.01

2.14

1.5

3.4

 

Our results for maturity agree with Kanwar et al. (2020), who found highly significant differences for a set of 25 genotypes evaluated in a Latin square design. Likewise, Dabi et al. (2017) evaluated 12 wheat genotypes and found a CV of 1.98% for maturity interval. Rana et al. (2023) also support the current mean range for maturity interval, which varied between 146-153 days for 40 genotypes. The heritability estimates disagree with the previously obtained results by Arya et al. (2017), who found that 17% was low in heritability for the maturity interval. Further results were drawn by Bhushan et al. (2013), whereby a set of 40 wheat genotypes in a randomized full-block design emerged with a high heritability of 77.5% for days to maturity. Experimental results may be inconsistent because of variations in the genetic material under experimentation.

Plant Height (cm)

The results of the analysis of variance showed that changes from genotype to genotype, for this parameter, were highly significant (P≤ 0.01) (Table 3). The CV was 2.02% for plant height. The overall mean plant height of the genotypes was 88.6 cm, with a minimum value of 80.7 cm and a maximum of 97.0 cm. PIRSABAK-21 showed the shortest plant height of 80.7 cm, while GULZAR-19 and DILKASH-21 showed the highest plant height of 97.0 cm (Table 5 and Figure 3). In the case of plant height, the LSD 5% was 2.0 cm. Heritability estimated for plant height was 0.90, and genetic advancement was 5.75. Low genetic improvement and high heritability were noticed for plant height.

Likewise, Gerema et al. (2020) evaluated 10 wheat genotypes and reported a CV of 6.6% for plant height. Kanwar et al. (2020) also confirmed that the mean range for plant height varied between 71-95 cm for 25 genotypes. Current means for plant height are supported by Kanwar et al. (2020), who found highly significant differences in the evaluation of 25 genotypes using a Latin square design. Furthermore, heritability results were confirmed by early researchers like Nukasani et al. (2019) found high heritability (92%) for plant height. Likewise, Bhushan et al. (2013) reported high heritability (97.6%) for plant height during the evaluation of 40 wheat genotypes in a randomized complete block design. Similarly, Din et al. (2018) reported a genetic advance of about 11.81 for plant height observed in the screening of 23 genotypes.

 

 

Flag leaf area (cm2)

Analysis of variance conducted on the flag leaf area showed very significant differences between genotypes at P≤ 0.01 (Table 3). The coefficient of variation for this parameter was 2.10%. Means ranged from 16.2 to 31.7 cm2 for the genotypes, with a value of 17.6 cm2. The smallest flag leaf area, 16.2 cm2, was recorded for SHAHKAR-13, and the largest, 31.7 cm2, for PIRSABAK-21 (Figure 4/Table 3). LSD at 5% for the flag leaf area was 2.1 cm2, and 0.86 was the heritability estimate of the flag leaf, while genetic progress was 3.51 (Table 7). The flag leaf area showed low genetic progress accompanied by high heritability (Table 7).

Our results for the flag leaf area agree with Kanwar et al. (2020), who found highly significant differences for a set of 25 genotypes evaluated in a Latin square design. Likewise, Dabi et al. (2017) evaluated 12 wheat genotypes and found a CV of 1.98 % for the flag leaf area. Ahmad et al. (2023) also confirmed mean range for flag leaf area varied between 21.29-36.41 cm2 for 10 genotypes. A high heritability of 92% has been reported for plant height by Arya et al. (2017). Likewise, Bhushan et al. (2013) observed high heritability (97.6%) for plant height during the evaluation of 40 wheat genotypes in a randomized complete block design. Similarly, Iqbal et al. (2017) reported a genetic advance of about 2.63 for flag leaf screening in 16 genotypes (Table 4).

Peduncle length (cm)

According to the results of the analysis of variance (Table 3), the difference in genotypes demonstrated

 

 

a highly significant effect on peduncle length (P ≤ 0.01). The CV of peduncle length was 1.50%. The mean pedicle length of the genotypes was 30.27 cm, ranging between 23.00 to 33.33 cm. The NIA ZARKHAIZE had the least peduncle length of 23.00 cm, and ZARGHOON-21 had the maximum peduncle length of 33.33 cm (Figure 5/Table 5). The 5% LSD was 1.5 cm for peduncle length, the heritability of a peduncle was 0.88, and the genetic advance was 2.75. Low genetic advance is predicted for peduncle length, and high heritability (Table 7).

Our results for peduncle length are supported by Gerema et al. (2020), who found highly significant differences in the evaluation of 180 genotypes using an alpha lattice design. The results of Rana et al. (2023) also support the current mean range for peduncle length varied between 37 to 67 cm for 40 genotypes. Heritability value is also in agreement with the early researchers like Bishwas et al. (2024), who found a high heritability of 78% for peduncle length. Adhikari et al. (2019) reported a genetic advance of about 1.53% for peduncle length in the screening of 26 genotypes.


Tillers m-2

Significant differences were observed at P≤0.01 among the genotypes for tillers m-2 (Table 3). Correspondingly, the CV was 3.39 for tillers per square meter. Average tiller m-2 was 253.31 with a range between 116.00 and 440.00. A maximum number of tillers m-2 (440.00) was recorded on F. BAKKAR, whereas PR-49 had the least number of tillers m-2 (116.00) (Figure 6/Table 7). More specifically, an LSD of 5% for tillers m-² was 3.39 with the smallest significant difference. The heritability value of tillers m-² was 0.88, and the genetic advance was equal to 2.75. Tillers have low genetic advancement and considerably high heritability (Table 7).

 

Present results for tillers m-2 are recorded by Prasad et al. (2021), where they found highly significant differences in the evaluation of 50 genotypes using a randomized complete block design. The findings of Varsha et al. (2019) also support the current mean range for tillers m-2 varied between 94.00 to 115.00 cm for 98 genotypes. Chauhan et al. (2023) reported a high heritability (83.6%) for tillers in the evaluation of 40 wheat genotypes in a randomized complete block design. Similarly, Ahmad and Gupta (2023) reported a genetic advance of about 1.76 for tiller screening of 10 genotypes.

Spike length (cm)

The length of spikes showed highly significant (P≤ 0.01) variations among genotypes for spike emergence (Table 4). The CV for spike length was 3.75%, while the mean spike length was 9.86 cm, with a range of 7.98 to 12.48 cm among the genotypes. The minimum spike length was recorded for KHYBER-23 (12.48cm), while the maximum was noted for ZARGHOON-21 (7.98 cm) (Figure 7/Table 5). The least significant difference (LSD 5%) for spike length was 0.75 cm. The heritability estimate of spike length was 0.86, while genetic advance was 1.23. A high heritability coupled with low genetic advance was recorded for spike length (Table 7).

Kyosev and Desheva (2015) also supported the current mean range for spike length varied between 9.20-17.60cm for 32 genotypes evaluated during 2014. The heritability result is also confirmed by early researchers like Desheva and Kyosev (2015), who found a high value of 83% for spike length. Rana et al. (2023) found lower genetic progress at 2.64, with a high heritability of 74% in the screening of 40 wheat genotypes in a randomized complete block design.

Spikelet spike-1

Genotype differences for spikelet spike-1 were highly significant with P≤0.01 based on the value of the mean squares (Table 4). The coefficient of variation computed for spikelet spike-1 was 4.67%. The spikelet counts ranged from 14.83 to 20.83, with an average of 18.08 spikelets spike-1. The lowest spikelet spike-1 was recorded for ZARGHOON-21, and the highest was found in MARKAZ-19, which had 20.83 (Figure 8/Table 6). A 1.70 was the least significant difference with an LSD of 5% for spikelets spike-1. The heritability value of 0.70 was obtained for the spikelets spike-1, and the genetic advance was 1.53. A minimum genetic advance with high heritability was observed for the spikelets (Table 7).

Our results on the number of spikelets per spike agree with the very significant differences Dragove et al. (2022) reported. Tefera et al. (2022) estimated a CV of 5.3% on a set of 81 genotypes tested in a triple lattice design in the same year. In the evaluation of 50 genotypes by Prasad et al. (2021), the range for spikelets per spike was confirmed to average between 14.10 to 21.23. In addition, for 180 wheat genotypes evaluated under alpha lattice design, Gerema et al. (2020) reported high heritability (60%) coupled with low genetic gain (21.1) in spikelets spike-1. This difference in findings might be attributed to variations in the genetic material used in experiments.

 

Table 6: Mean performances of wheat advanced lines for Spike length Spikelets spike-1, thousand-grain weight, grain yield, biological yield, and harvest index at CCRI during 2022-23.

Varieties

Spike length(cm)

Spikeletsspike-1

Thousand-grainweight(g)

Biological yield (Kg ha-1)

Grain yield
(Kg ha
-1)

Harvest index

PR-149

9.5

20.7

38.9

10000

3440

36.5

PR-152

9.5

18.3

42.9

9750

3775

36.4

PR-153

9.9

18.5

49.2

8500

4365

40.4

PR-154

10.6

17.5

38.3

9500

3435

30.0

PR-155

9.2

17.5

47.8

8000

4745

43.4

PR-156

9.5

17.3

40.0

7750

4100

44.0

PR-157

10.0

19.7

43.6

11500

4340

40.1

PR-158

9.6

16.8

42.1

12000

4020

35.8

PIRSABAK-13

9.3

17.5

44.2

10500

4320

38.3

SHAHKAR-13

9.6

18.2

36.9

10500

3735

32.8

PIRSABAK-15

9.3

17.7

40.1

11000

5290

41.7

PASEENA-17

9.4

18.5

41.0

11500

4010

40.0

WADAN-17

11.5

16.7

39.1

11750

3665

32.4

KHAISTA-17

9.8

20.3

44.3

11000

4675

37.8

PIRSABA-19

9.9

18.3

33.8

13000

3995

34.1

GULZAR-19

9.1

17.3

40.2

11250

3890

37.2

ABASEEN-21

9.1

15.7

38.1

12000

3800

33.8

ZARGHOON-21

8.0

14.8

42.1

11000

4375

35.2

PIRSABAK-21

8.8

20.5

41.0

10000

3770

37.2

TASKEEN-22

9.6

17.3

37.2

12500

4020

36.1

PIRSABAK-23

10.5

16.2

42.9

13250

4315

37.1

KHYBER-23

12.4

17.3

45.9

10500

3455

37.7

ABDUL BARI-24

9.5

17.0

43.2

9500

3875

41.6

FAHIM-19

9.7

18.7

41.6

9750

4070

38.5

KT-17

10.7

18.5

34.8

10750

4010

36.5

TANDA-23

10.7

18.0

42.7

7500

3970

52.1

SWABI-1

9.0

17.0

38.9

8750

4235

46.4

NAURANG-23

10.6

16.3

41.1

9750

3465

35.4

TARNAB RAHBER

9.5

18.0

43.2

11750

3495

33.6

TARNAB GANAM

8.9

15.7

40.3

9000

3320

32.3

NIFA LALMA

9.4

16.7

44.5

10500

4550

36.6

NIFA NIJAT

8.5

18.5

31.6

8750

2870

32.9

FAHR E NIFA

10.5

16.3

34.7

9500

3655

34.7

WAFAQ-23

10.5

19.2

43.7

7250

3000

37.2

NARC SUPER

11.3

19.3

39.0

11500

4170

36.9

MARKAZ-19

9.9

20.8

35.7

9500

2745

33.7

BORLUG-16

9.4

18.3

38.5

9500

3480

25.6

ZINCOL16

11.3

16.3

40.2

8250

3465

35.3

MA-20

8.8

19.3

29.5

5375

3160

46.3

AKBAR-19

9.4

17.7

27.0

7000

1375

23.5

DILKASH-21

11.2

17.7

40.5

7500

2665

36.4

UROOJ-2022

10.5

20.5

42.4

9000

3935

29.4

GHAZI-19

9.8

19.3

39.4

8750

3200

33.4

NAWAB-21

11.0

18.0

39.6

10750

3730

37.6

NIA SHAHEEN

11.2

18.7

38.8

8500

2750

36.0

NIA SUNHERI

8.2

18.7

35.6

8500

3315

34.5

NIA ZARKHAIZE

8.2

19.3

29.1

6250

2100

27.5

F.BAKKAR

10.0

20.7

36.6

9000

3490

32.2

BAKKAR STAR

11.7

18.8

43.6

11250

3600

31.9

GM

9.9

18.1

39.7

9798.5

3698.4

36.2

LSD

0.8

1.7

0.7

127.1

566.1

1.5

 

 

1000-grain weight (gm)

The means squares of different genotypes differ in 1000-grain weight very significantly (P≤ 0.01) (Table 4). The coefficient of variation calculated for 1000 grains was 0.85%. The average value for 1000-grain weight for each genotype was 18.50 g, having a range of 27.00–49.20 g. The maximum weight for 1000 grains (49.20 g) was recorded for PR-153, while AKBAR-19 has the least weight for 1000 grains (27.00g) (Figure 9/Table 5). A 2.21 g was the least significant difference (LSD 5%) for 1000-grain weight. At 1000 grain weight, the heritability estimate was 0.99, and genetic progress was 6.13. High heritability with very low genetic progress was observed for the predicted thousand-grain weight (Table 7).

Our results for the 1000-grain weight were following Varsha et al. (2019), in which significant differences were found for the set of 98 genotypes evaluated in a randomized block design in the year 2019. Likewise, Wani et al. (2018) evaluated 24 wheat genotypes and found a CV of 0.57 % for 1000-grain weight. Din et al. (2018) also supported the current mean range for thousand-grain weight varied between 34.3-41.7cm

 

 

for 23 genotypes. The estimate for thousand-grain weight had a heritability value of 95%, matching that of previous early researchers, Chauhan et al. (2022). In subsequent works, Nukasani et al. (2011) obtained 114 genotypes in an RFB design with three replications, resulting in a high heritability of 96 %, which disagrees with that of Ahmad et al. (2023), conforming to the current 4.89% genetic advance (Table 7).

Biological yield (Kg ha-1)

Variance analysis of biological yield showed significant changes from genotype to genotype at P≤0.01 (Table 4). The coefficient of variation (CV) estimated for biological yield was 0.64%. The mean values for biological yield ranged from 13250.00 to 5375.00 with an average of 9798.47(Table 6). The minimum biological yield (13250.00) was documented for PIRSABAK-23, whereas the maximum biological yield (5375.00) was recorded for MA-20 (Figure 10/Table 6). The least significant difference (LSD 5%) for biological yield is 127.05. The heritability estimate of biological yield was 0.998, while genetic advance was 2257.43 (Table 7).

Our results for biological yield are in agreement with Bishwas et al. (2024), who found highly significant differences for a set of 20 genotypes evaluated in a randomized block design. Rana et al. (2023) also observed mean range for bio yield varied between 20 and 52 for 40 genotypes. These results are supported by an estimated significant heritability of 93% for bio-yield (Arya et al., 2017). Moreover, Bhushan et al. 2012 observed a high heritability of 92% in 30 genotypes in a randomized block design with three replications. On the other hand, Iqbal et al. (2017) reported a genetic gain of 19.28%.

Grain yield (Kg ha-1)

There was a significant variation in grain yield (P≤ 0.01) among genotypes (Table 4). Coefficients of variation computed for grain yield were 8.98%. Grain yield ranged from 2916 to 5784 Kg ha-1, averaging 4457.13 Kg ha-1. PIRSABAK-13 had the highest grain yield, while SWABI-1 had the lowest grain yield with 2916.19 Kg ha-1 (Figure 11/Table 6). In the case of grain yield, the LSD 5% was 802.18 Kg ha-1. The heritability for grain yield was estimated at 0.84, and the genetic progress was 820.75. The grain yields manifested significant genetic progress with high heritability (Table 7).

In the grain yield, our results agree with Chauhan et al. (2022), who found highly significant differences for the set of 40 genotypes tested in a randomized whole-block design. Iqbal et al. (2017) reported a CV of 11.50% for grain yield by evaluating 16 wheat genotypes. The heritability value is also similar in magnitude to the findings of Bhushan et al. (2009), with a high heritability of 78% for grain yield. Likewise, Bhushan et al. (2009) also reported a high heritability (92%) by observing 30 genotypes in an RBD with three replications. A heritability value as high as 79% and genetic advance of 103.79 for genotype 114 were also recorded in an RBD design with three replications by Nukasani et al. (2011). In contrast, Bayisa et al. (2020) reported about 10.38% genetic gain. Contradictions in genetic advancement may be the case due to variations in the genetic material used in those experiments.

Harvest index

On the harvest index, ANOVA showed genotype significant differences at (P≤0.01) (Table 4). The coefficient of variation (CV) estimated for the harvest index was 2.08%. Mean values for the harvest index ranged from 23.50 to 52.13 Kg ha-1 with an average of 36.24 Kg ha-1 (Table 6). The minimum harvest index (23.50 Kg ha-1) was documented for AKBAR-19, whereas the maximum harvest index (52.13 Kg ha-1) was recorded for TANDA-23 (Figure 12/Table 7). The least significant difference (LSD 5%) for harvest index (Kg ha-1) was 1.52 Kg ha-1. The heritability estimate of harvest index was 0.98, while genetic advance was 6.92. The harvest index presents rather low genetic progress associated with high heritability (Table 7).

Our results for the harvest index are in agreement with those of Prasad et al. (2021), who found highly significant differences for a set of 50 genotypes evaluated in a randomized block design. Likewise, Dabi et al. (2017) evaluated 12 wheat genotypes with a CV of 10.1 % for the harvest index. Kanwar et al. (2018) also observed mean range for the harvest index varied between 30.0-64% for 98 genotypes. These outcomes concur with those of other research, including Varsha et al. (2019), who found that the harvest index had a high heritability value of 96%. A related study by Bhushan et al. (2009) also detected a high heritability of 92%, using 30 genotypes and three replications in a randomized block design. While Rajput et al. (2019) observed a genetic advance of about 8.73%.

Phenotypic and genotypic correlation

Days to heading and days to maturity expressed a highly significant positive phenotypic relationship, rP = 0.89, P = 0.01, about the harvest index, P = 0.01, and rP = 0.64. On the other hand, days to heading showed a strongly negative phenotypic connection with the biological yield (rP = 0.35, P = 0.05) and tillers meter-2 (rP = -0.42, P = 0.01) (Table 8). Similar correlations between heading and bio-yield (rp=-0.19*) were

 

Table 7: Estimation of genetic, environmental and phenotypic variance with their respective heritability and genetic advance for various traits.

Name of Traits

Genetic Variance (Vg)

Environmental Variance (Ve)

Phenotypic Variance (Vp)

Heritability

(h2)

Genetic Advance (GA)

Days to heading

19.24

0.39

19.63

0.98

6.12

Days to Maturity

0.76

1.46

2.22

0.34

0.72

Plant Height

18.42

1.98

20.39

0.90

5.75

Flag Leaf Area

7.16

1.12

8.28

0.86

3.51

Peduncle Length

4.29

0.57

4.86

0.88

2.75

Tillers metre-2

7579.75

2.82

7582.57

0.98

122.73

Spike Length

0.88

0.14

1.02

0.86

1.23

Spikelets Spike-1

1.68

0.71

2.39

0.70

1.53

Thousand Grain weight

19.02

0.11

19.13

0.99

6.13

Grain Yield

404712.61

78695.94

483408.55

0.84

820.75

Biological Yield

2768239.64

3963.19

2772202.83

0.98

2344.28

Harvest Index

24.62

0.57

25.19

0.98

6.92

 

 

also recorded by Rana et al. 2023 in their research. Mecha et al. (2017) and Gerema et al. (2020) observed the same relationship between heading and maturity in their respective experiments (rG=0.42** and rG=0.39**), respectively. Days to maturity showed a positive phenotypic association with harvest index (rP = 0.43, P = 0.01), and thousand-grain weight (rP = 0.29, P = 0.05). The same relationship between plant height and maturity, rG=0.53*, was reported by Abinasa et al. (2011) for a set of 16 durum genotypes. Plant height and peduncle length showed significant positive phenotypic relationships (rP=0.83, P = 0.01; flag leaf area, rP=0.35, P = 0.05). Moreover, a significant negative correlation between the plant height and the harvest index, tillers meter-2, grain yield, bio yield, and spikelets spike-1, with corresponding rP values of -0.35, P = 0.05, -0.52, P = 0.01, -0.36, P = 0.05, -0.48, P = 0.01, and rP values of -0.29 and P = 0.05 (Table 8). Ibrahim et al. (2010) demonstrated a strong positive phenotypic correlation between plant height and 1000-grain weight (rp=0.31*) and flag leaf area (rp=0.50**), further validating the current association. In this regard, Khaliq et al. (2004) reported a high positive phenotypic association rP =0.82** between plant height and spikelets spike-1.

Flag leaf area and plant height were strongly positively genotypically associated rG= 0.37, P=0.05. On the other hand, spikelets spike-1 and biological yield had a strong negative genotypic association with the plant height (Table 6). Upadhyay et al. (2020) observed almost similar associations, viz., a positive significant genotypic correlation between plant height and peduncle length, rG=0.88**; and Rahman et al. (2017) showed a similar correlation between plant height and spikelets spike-1, rG=0.79**. Similarly, Khaliq et al. (2004) found a significant positive genotypic association of Q = 0.76* existing between plant height and flag leaf area. More recently, Ibrahim et al. (2020) revealed a positive genotypic correlation rp=0.52**, between plant height and 1000-grain weight.

On the other hand, flag leaf area and spike length, rP= 0.45, P = 0.01, peduncle length, rP= 0.80, P = 0.01, indicated a strong positive phenotypic relationship. According to this, there was a highly significant negative association (rP = -0.41 at P = 0.01) and positive relationship (rP = 0.32 at P = 0.05) between the tillers meter-2 and bio-yield and leaf area, respectively (Table 8). In contrast, flag leaf area and peduncle length were highly significantly positively associated on a genotypic basis, rG = 0.45 at P = 0.01. Iqbal et al. (2017), tested 16 genotypes in a randomized complete block design and established the same relationship of flag leaf area with bio-yield, rG=0.30*.

The peduncle length correlated significantly negatively with biological yield, while it correlated positively with spike length with rP = -0.35 and rP = 0.78, respectively at P = 0.01. The peduncle length correlated significantly positively with spike length and negatively with tillers meter-2, with rG = 0.35 and rG = -0.42, respectively, at P = 0.05 (Table 7). Ullah et al. (2021) reported the same magnitude of peduncle length with spikelets per spike, rG = 0.78**.

The spikelets, however, recorded negative phenotypic association with harvest index, rP=-0.35, P = 0.05, and with bio-yield, rP= – 0.72, P = 0.01. Similarly, spikelets spike-1 and tillers meter-2 also recorded a positive association, rP=0.59, P=0.01 (Table 7). Bishwas and Singh (2024) led to the same conclusion about the association of spikelets spike-1 and bio-yield with rG=0.9345** from their experiments, consisting of 20 genotypes in a block design. Chauhan et al. (2022) reported the morphological and genotypic association between spikelets and bio-yield as rG= 0.440** and rP= 0.395**. The phenotypic association between tillers and bio-yield showed a strong positive association with rP= 0.35, P = 0.05.

The tillers, however, were negatively correlated to the harvest index with rP =-0.72 at P = 0.01 and thousand-grain weight with rP =-0.34 at P = 0.05. However, a strong positive genotypic association, rG= 0.55 at P = 0.01, was found to exist between tiller meter-2 and grain yield. However, a significant negative genotypic association was observed between tiller meter-2 and harvest index with rG=-0.33 at P = 0.05. Gao et al. (2024) revealed the presence of a negative relationship between tiller meter-2 and chlorophyll content, rG = 0.36*. Kiss et al. (2021) reported an identical finding of a strong negative genotypic association between tiller meter-2 with 1000-grain weight; rG= -0.60**. Similarly, 1000-grain weight and tiller meter-2 showed a strong negative phenotypic association rP= -0.44**. The phenotypic relation of grain yield and biological yield was highly significant, rP = 0.87, P = 0.01, while the harvest index showed a negative relationship, rP = 0.40, P = 0.01.

Furthermore, the biological yield and grain yield exhibited a highly positive genotypic relationship, rG= 0.73, P = 0.01 (Table 8). According to Bayisa et al. (2020), there was a high positive genotypic association between grain yield and biological yield, rG= 0.62**. Furthermore, Din et al. (2018), indicated that there existed a positive genotypic correlation between grain yield and bio-yield, rG== 0.961**. A high positive phenotypic and genotypic correlation between the thousand-grain weight and harvest index, with rP = 0.54, P = 0.01, and rG = 0.50, P = 0.01, respectively (Table 8). Chauhan et al. (2022) estimated the correlations of genotype and phenotype with the harvest index to be rG = 0.378** and 0.384**, respectively.

Conclusion and Recommendations

Our analysis of the 49 different wheat genotypes revealed significant variations across various phenological and morphological traits. Among these genotypes, some of them were identified for specific traits, like PR-156 for early maturity, NIA ZARKHAIZE for the highest tillers per square meter, PR-153 for the highest 1000-grain weight, PIRSABAK-15 for the highest grain yield, and PIRSABAK-23 for the highest biological yield. Significant positive genotypic correlations were observed among various key traits including days to heading with maturity and harvest index, maturity with plant height, plant height relative to the flag leaf area, spike length relative to spike-1, tillers relative to grain yield, and grain yield with biological yield and 1,000-grain weight relative to the harvest index. These are the indicators of the possibility of charting improvement at the same time in the right proportion through the breeder’s effort and coordination in genetic management. All these correlations show coordinated potential for simultaneous improvement through breeding efforts.

We recommend that some of the enhancing traits, such as early maturity, tillering capacity, grain yield, 1000-grain weight, and biological yield, can be considered for future breeding programs, as well as efforts need to utilize advanced techniques for more efficient trait improvement. Further research can help in understanding the trait relationships, and leveraging advanced breeding technologies will be crucial for developing high-yielding and resilient wheat varieties to address agricultural challenges.

Acknowledgements

We are thankful to the Cereal Crop Research Institute (CCRI), Pirsabak Nowshera, Pakistan, for providing the research materials and facilitating this project, as well as the Department of Botany, AWKUM.

Novelty Statement

The field trial of 49 different wheat genotypes revealed that genotypes PR-156, Nia Zarkhaize, and PR-153 had the earliest maturity, the highest tillers per square meter, and 1000-grain weight, respectively. Furthermore, Pirsabak-15 and Pirsabak-23 had the highest grain and biological yields, respectively.

Author’s Contribution

Zarghoona: Research experiment executed/MS drafting

Khilwat Afridi: Field trial supervision

Ruby Wali Khan, Rahmat Elahi, Nadia, Kashmala Jabbar, Guleena Khan, Haleema Bibi and Haseeba: Data collection

Ikramullah Khan: Proofreading

Abdur Rauf: Research Supervision/MS drafting and proofreading.

Generative AI and AI-assisted technology statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

Conflict of interest

The authors have declared no conflict of interest.

References

Abdulhamed, Z.A., Abood, N.M. and Noaman, A.H., 2021. IOP Conf. Ser. Earth Environ. Sci., 761: 012066. https://doi.org/10.1088/1755-1315/761/1/012066

Abinasa, M., Ayana, A. and Bultosa, G., 2011. Genetic variability, heritability and trait associations in durum wheat (Triticum turgidum L. var. durum) genotypes. African J. Agric. Res., 6(17): 3972-3979.https://doi.org/10.5897/AJAR10.880

Adhikari, A., Ibrahim, A.M.H., Rudd, J.C., Baenziger, P.S. and Sarazin, J.B., 2019. Estimation of heterosis and combining abilities of U.S. winter wheat germplasm for hybrid development in Texas. Crop Sci., 60(2): 788-803.

Ahmad, A. and Gupta, R.K., 2023. Genetic variability, heritability and genetic advance for yield and yield associated traits in bread wheat (Triticum Aestivum L.). Ann. Agric. Crop Sci., 8(1): 1125.

Ahmad, D., Afzal, M. and Rauf, A., 2020. Environmental risks among rice farmers and factors influencing their risk perceptions and attitudes in Punjab, Pakistan. Environ. Sci. Pollut. Res, 27.21953-21964.https://doi.org/10.1007/s11356-020-08771-8

Ahmad, J,. Rehman, A., Ahmad, N., Anwar, J., Nadeem, M., Owais, M., Abdullah, M., Gulnaz, S., Ramzan, Y., Shair, H., Saleem, M., Shahzad, R., 2023. Dilkash-20: A newly approved wheat variety recommended for Punjab, Pakistan, with supreme yielding potential and disease resistance. SABRAO J. Breed. Genet. 55(2): 298-308. http://doi.org/10.54910/sabrao2023.55.2.3

Amin, A., Nasim, W., Mubeen, M., Nadeem, M., Ali, L., Hammad, H.M. and Fathi, A., 2017. Optimizing the phosphorus use in cotton by using Csm-Cropgro-cotton model for semi-arid climate of Vehari-Punjab, Pakistan. Environ. Sci. Pollut. Res., 24, 5811-5823.https://doi.org/10.1016/j.fcr.2017.07.007

Arya, V., Singh, J., Kumar, L., Kumar, R. and Kumar, P., 2017. Genetic variability and diversity analysis for yield and its components in wheat (Triticum aestivum L.). Indian J. Agric. Res., 51(2), 128-134. https://doi.org/10.18805/ijare.v0iOF.7634

Arzadun, M.J., Arroquy, J.I., Laborde, H.E. and Brevedan, R.E., 2006. Effect of planting date, clipping height, and cultivar on forage and grain yield of winter wheat in argentinean pampas. Agron. J., 98: 1274–1279. https://doi.org/10.2134/agronj2005.0313

Balkan, A., 2018. Genetic variability, heritability and genetic advance for yield and quality traits in M2-4 generations of bread wheat (Triticum aestivum L.) genotypes. Turk. J. Field Crops, 23(2): 173-179.

Bayisa, T., Tefera, H. and Letta, T., 2020. Genetic variability, heritability and genetic advance among bread wheat genotypes at Southeastern Ethiopia. Agric. Forestr. Fish., 9(4): 128-134. https://doi.org/10.11648/j.aff.20200904.15

Bhargava, A., Shukla, S., Katiyar, S. and Ohri, D., 2003. Selection parameters for genetic improvement in Chenopodium grain yield in sodic soil. J. Appl. Horticult., 5: 45-48.https://doi.org/10.37855/jah.2003.v05i01.13

Bhushan, B., Bharti, S., Ojha, A., Pandey, M., Gourav, S.S., Tyagi, B.S. and Singh G., 2013. Genetic variability, correlation coefficient and path analysis of some quantitative traits in bread wheat. J. Cereal Res., 5(1).https://doi.org/10.1002/agg2.20515

Bishwa,s S. and Singh, B., 2024). Assessment of heritability, genetic advance and correlation coefficient in wheat (Triticum aestivum L.). Int. J. Plant Soil Sci., 36(1), 82-88.https://doi.org/10.18805/IJARe.A-5095

Chauhan, S., Tyagi, S.D., Gupta, A. and Singh, S., 2022. Genetic variability, correlation, path coefficient and cluster analysis in bread wheat (Triticum aestivum L.) under rainfed conditions. Pharma Innovat. J., 11(11), 818-823.

Dabi, A., Mekbib, F. and Desalegn, T., 2019. Genetic variability studies on bread wheat (Triticum aestivum L.) genotypes. J. Plant Breed Crop Sci., 11(2), 41-54.https://doi.org/10.5897/JPBCS2016.0600

Desheva, G. and Kyosev, B., 2015. Genetic diversity assessment of common winter wheat (Triticum aestivum L.) genotypes. Emirates J. Food Agric., 27(3), 283.https://doi.org/10.9755/ejfa.v27i3.19799

Del-Moral, L.F., Rharrabti, Y., Villegas, D., and Royo, C., 2003. Evaluation of grain yield and its components in durum wheat under Mediterranean conditions. Agron. J., 95(2): 266–274. https://doi.org/10. 2134/agronj2003.0266

Desheva, G. and Kyosev, B., 2015. Genetic diversity assessment of common winter wheat (Triticum aestivum L.) genotypes. Emirates J. Food Agric., 27(3): 283. https://doi.org/10.9755/ejfa.v27i3.19799

Din, I., Munsif, F., Shah, I., Khan, A., Khan, H., Uddin, S. and Islam, T., 2018. Genetic variability and heritability for yield and yield associated traits of wheat genotypes in Nowshera Valley, Pakistan. Pak. J. Agric. Res., 31(3): 216-222. http://dx.doi.org/10.17582/journal.pjar/2018/31.3.216.222

Gao, G., Zhang, L., Wu, L. and Yuan, D., 2024. Estimation of chlorophyll content in wheat based on optimal spectral index. Appl. Sci.,14(2): 703. https://doi.org/10.3390/app14020703

Gelalcha, S., Hanchinal, R.R., 2013. Correlation and path analysis in yield and yield components in spring bread wheat (Triticum aestivum L.) genotypes under irrigated condition in Southern India. Afri. J. Agric. Res., 8(24): 3186-3192. https://doi.org/10.5897/AJAR2012.6965

Gerema, G., Lule, D., Lemessa, F. and Mekonnen, 2020. Morphological characterization and genetic analysis in bread wheat germplasm: A combined study of heritability, genetic variance, genetic divergence and association of characters. Agric. Sci. Technol., (1313-8820), 12(4). https://doi.org/10.15547/AST.2020.04.048

Habash, D.Z., Kehel, Z. and Nachit, M., 2009. Genomic approaches for designing durum wheat ready for climate change with a focus on drought. J. Exp. Bot., 60: 2805-2815.

Hancock, J.F.E., 2003. Plant evolution and the origin of crop species. CABI publishing.https://doi.org/10.1017/S0014479712001457

Ibrahim, A., Yadav, B., Anusha, R. and Magashi, A.I., 2020. Heterosis studies in durum wheat (Triticum durum L.). J. Genet. Genom. Plant Breed, 4(1), 2-8.https://doi.org/10.32406/v7n3/2024/102-114/agrariacad

Iqbal, A., Khalil, I., Shah, S.M.A. and Kakar, M.S., 2017. Estimation of heritability, genetic advance and correlation for morphological traits in spring wheat. Sarhad J. Agric., 33(4), 674-679.https://doi.org/10.1016/j.jksus.2022.102364

Kanwar, A., Agrawal, A., Sharma, P.J. and Agrawal, H.P., 2020. Genetic parameters of variation and correlation analysis in wheat under terminal heat stress. J. Pharma. Phytochem., 9(5), 1795-1798.https://doi.org/10.3389/fpls.2023.1132108

Kiss, T., Balla, K., Cseh, A., Berki, Z., Horvath, A., Vida, G., Veisz, O. and Karasi, I., 2021. Assessment of the genetic diversity, population structure and allele distribution of major plant development genes in bread wheat cultivars using DArT and gene-specific markers. Cereal Res. Commun., 49: 549–557 https://doi.org/10.1007/s42976-021-00136-2

Khaliq, I., Parveen, N. and Chowdhry, M.A., 2004. Correlation and path coefficient analyses in bread wheat. Int. J. Agri. Biol. 6(4).

Khan, A., Azam, J. and Ali, F., 2010. Relationship of morphological traits and grain yield in recombinant inbred wheat lines grown under drought conditions. Pak. J. Bot., 42(1): 259-267.https://doi.org/10.1016/j.cj.2023.05.002

Khan. T., Gul, S., Khan, N.U., Fawibe, O., Akhtar, N., Rehman, M., Sabah, N., Tahir, M.A., Iqbal, A., Naz, F., Haq, I. and Rauf, A., 2023). Stability analysis of wheat through genotype by environment interaction in three regions of Khyber Pakhtunkhwa, Pakistan. SABRAO J. Breed. Genet., 55(1): 0-0. http://doi.org/10.54910/sabrao2023.55.1.

Mangova, M. and Rachovska, G., 2004. Technological characteristics of newly developed mutant common winter wheat lines. Plant Soil and Environ., 50(2), 84-87.https://doi.org/10.17221/3686-PSE

Manivannan, N., 2014. TNAUSTAT-Statistical package. Retrieved from https://sites.google.com/site/tnaustat.

Mecha, B., Alamerew, S., Assefa, A., Assefa, E. andDutamo, D., 2017. Correlation and path coefficient studies of yield and yield-associated traits in bread wheat (Triticum aestivum L.) genotypes. Adv. Plants Agric. Res., 6(5): 128-136.

Muhammad, S., Anjum, A.S., Kasana, M.I. and Randhawa, M.A., 2013. Impact of organic fertilizer, humic acid and sea weed extract on wheat production in Pothowar region of Pakistan. Pak. J. Agric. Sci., 50(4), 677-681.https://doi.org/10.21162/PAKJAS

Nawaz, H., Shah, S., Rab, A., Fayyaz, H., Raza, H.K., Hairs, T.J. and Ahmad, S.J., 2017. Response of wheat cultivars toward successive delayed sowing under rainfed condition in Lower Dir. Pure Appl. Biol., (PAB), 6(2), 470-480.http://dx.doi.org/10.19045/bspab.2017.60046

Nukasani, V., Potdukhe, N.R., Bharad, S., Deshmukh, S. and Shinde, S.M., 2013. Genetic variability, correlation and path analysis in wheat. J. Cereal Res., 5(2). https://doi.org/10.11648/j.abb.20231103.13

Piepho, H.P., Möhring, J., Schulz-Streeck, T. and Ogutu, J.O., 2012. A stage-wise approach for the analysis of multi-environment trials. Biom J., 54(6): 844-60. https://doi.org/10.1002/bimj.201100219

Prasad, J., Dasora, A., Chauhan, D., Rizzardi, D.A., Bangarwa, S.K. and Nesara, K., 2021. Genetic variability, heritability and genetic advance in bread wheat (Triticum aestivum L.) genotypes. Gen. Mole. Res., 20(2), 1-6.http://dx.doi.org/10.4238/gmr19419

Rana, P., Bıshno, O.P., Chaurasıa, H. and Behl, R.K., 2023. Genetic Variability and Correlation Coefficient Analysis in Wheat Genotypes for Grain Yield and Its Contributing Traits under Drought and Irrigated Condition. Ekin J. Crop Breed. Gen., 9(2), 150-159.https://doi.org/10.1186/s43170-024-00259-6

Rahman, M.M., Mandal, M.S.N., Alam, M.A., Rahman, S., Begum, N. AND Khalil, I.H., 2017. Identification of drought-tolerant spring wheat genotypes based on some of the physiological traits. SABRAO J. Breed. Genet., 49 (1): 104-115.

Rajput, R.S., 2019. Path analysis and genetic parameters for grain yield in bread wheat (Triticum aestivum L.). Annual Res. Rev. Biol., 31(3): 1–8.

Rauf, A., Jawad, M., Jan, F., Qayash, M., Yasin, M., Gul, S., Khan, W., Khan, I., Bibi, F., Khan, W., Kumar, T., Aarif, M. and Afridi, K., 2023. Comparative performance of diverse advanced wheat genotypes in response to different sowing times. Pak. J. Weed Sci. Res., 29(2): 72-80.

Rauf, A., Khan, M.A., Jan, F., Gul, S., Afridi, K., Khan, I., Bibi, H., Khan, R.W., Khan, W. and Kumar, T., 2023. Genetic analysis for production traits in wheat using line x tester combining ability analysis. SABRAO J. Breed. Genet., 55(2): 0-0. http://doi.org/10.54910/sabrao2023.55.2

Rauf, A., Sadiq, M., Jan, F., Qayash, M., Khan, W., Khan, I., Afridi, K., Shuaib, M., Khalid, M. and Gul, S., 2023. Comparative analysis of genetic variability and heritability in wheat germplasms. Pak. J. Weed Sci. Res., 39, no. 2: 95-101.

Sadiq, M., Nadia, A. Rauf, K. Afridi, M. Qayash, S. Yaqub, K. Jabbar, G. Khan, I. Khan, A. Khan, T. Ullah, T. Kumar, M. Arif, M. Ismail and M. Munir., 2025. Evaluation of genetic variability and yellow rust in selected wheat lines. Pak. J. Weed Sci. Res., 31(1): 16-36.

Salman, S., Khan, S.J., Khan, J., Khan, R.U. and Khan, I., 2014. Genetic variability studies in bread wheat. Pakistan J. Agric. Res., 27(1): 1–7.

Shafi, M., Khan, M.J., Bakht, J. and Khan, M.A., 2013. Response of wheat genotypes to salinity under field environment. Pak. J. Bot., 45(3), 787-794.https://doi.org/10.3389/fpls.2024.1396498

Shi, J., Gao, H., Wang, H., Lafitte, H.R., Archibald, R.L., Yang, M. and Habben, J.E., 2017. ARGOS 8 variants generated by CRISPR-Cas9 improve maize grain yield under field drought stress conditions. Plant Biotechnol. J., 15(2), 207-216.https://doi.org/10.1111/pbi.12603.

Tefera, H., 2022. Genetic variability, divergence, and path coefficient analysis of yield and yield related traits of Durum wheat (Triticum turgidum L. var. Durum) genotypes at Jamma district, south wollo zone, amhara region, Ethiopia. J. Plant Sci. Phytopathol., 6(2), 075-083.https://doi.org/10.29328/journal.jpsp.1001078

Upadhyay, S., Dubey, N., Yadav, P.S., Mishra, V.K., 2020. Estimation of heterobeltiosis and character associations for yield and yield attributing traits in bread wheat (Triticum aestivum L.) genotypes. Int. J. Curr. Microbiol. Appl. Sci., 9(4): 2734-2747.

Varsha, Verma, P., Saini, P., Singh, V., Yashveer, S., 2019. Genetic variability of wheat (Triticum aestivum L.) genotypes for agro-morphological traits and their correlation and path analysis. J. Pharmacog. Phytochem., 8(4): 2290-2294.

Wani, S.H., Sheikh, F.A., Najeeb, S., Sofi, M.U.D., Iqbal, A.M., Kordrostami, M. and Jeberson, M.S., 2018. Genetic variability study in Bread Wheat (Triticum aestivum L.) under Temperate Conditions. Curr. Agric. Res. J., 6(3).http://dx.doi.org/10.12944/CARJ.6.3.06