Comparison Among Different Stability Models for Yield in Bread Wheat
Comparison Among Different Stability Models for Yield in Bread Wheat
Malak Atiq Ullah Khan1*, Fida Mohammad2, Fahim Ullah Khan3, Sheraz Ahmad2, Mian Ahmad Raza1 and Tariq Kamal1
1Department of Agriculture, University of Swabi, Khyber Pakhtunkhwa, Pakistan; 2Department of Plant Breeding and Genetics, The University of Agriculture Peshawar, Khyber Pakhtunkhwa, Pakistan; 3Department of Agriculture, Hazara University Mansehra, Khyber Pakhtunkhwa, Pakistan.
Abstract | A critical comparison of stability models is essential to give an insight to breeders for developing relatively stable wheat cultivars. A multi-environment trial (MET) was conducted to assess the pattern of genotype by environment interaction (GEI) effects on yield using multiple stability models viz. Additive Main effect and Multiplicative Interaction (AMMI), GGE biplot analysis and stability parameters. Eighty-one wheat genotypes were evaluated during three consecutive years (2013/14, 2014/15 and 2015/16) across nine environments (sites × year combination) in Khyber Pakhtunkhwa, Pakistan. Graphical stability approaches such as AMMI and GGE provided almost similar results for identifying the high-yielding and stable wheat genotypes. The AMMI analysis identified G-58 and G-79, whereas GGE biplot identidified G-79 as the most stable and high yielding genotype. Numerical stability parameters like Eberhart and Russell’s model and Francis coefficient of variation (CV) declared G-79 as top-ranked genotype while Shukla stability value (σi2) and Wrick’s ecovalence (Wi) identified G-80 (check cultivar Janbaz), G-52 and G-79 as leading wheat genotypes based on grain yield. Spearman’s rank correlation revealed significant positive correlations of AMMI stability value (ASV) with CV, σi2 with Wi, and Wi with CV indicating that these parameters could invariably be used for identifying stable wheat genotypes depending upon the nature of the experiment, breeding material, and the complexity of data. Different stability models identified G-79 as high yielding and stable genotype and thus could be recommended for commercialization in the province of Khyber Pakhtunkhwa, Pakistan. Furthermore, stability parameters can supplement the use of AMMI and GGE biplot analysis to get more credible and reliable scrutiny of wheat genotypes in METs.
Received | April 30, 2019; Accepted | February 16, 2020; Published | February 25, 2020
*Correspondence | Malak Atiq Ullah Khan, Department of Agriculture, University of Swabi, Khyber Pakhtunkhwa, Pakistan; Email: dr.atiq@uoswabi.edu.pk
Citation | Khan, M.A.U., F. Mohammad, F.U. Khan, S. Ahmad, M.A. Raza and T. Kamal. 2020. Comparison among different stability models for yield in bread wheat. Sarhad Journal of Agriculture, 36(1): 282-290.
DOI | http://dx.doi.org/10.17582/journal.sja/2020/36.1.282.290
Keywords | GEI, AMMI analysis, GGE biplot, Stability parameters
Introduction
Wheat (Triticum aestivum L.) is a leading food grain which occupies more area than any other crop in Pakistan. Wheat contributes about 10.0 percent to the value-added in agriculture and 2.1 percent to GDP. In Pakistan, the main wheat-growing areas fall in the Indus plains. About 70% of the wheat is grown on irrigated land and 30% is grown under rain-fed conditions (Ain et al., 2015). The development of high yielding stable genotypes is a primary objective of all wheat breeding programs. Increasing the yield without sacrificing stability in performance is a great challenge for wheat breeders. The performance of cultivars largely depends on their genetic makeup, environment and the interaction between genotypes and environment. The response of genotypes varies across years and locations as a result of interaction between genotypes and the environment. Therefore, testing of wheat genotypes across years and location is essential (Abraha et al., 2019). Several stability methods including both univariate and multivariate have been proposed to analyze and interpret the performance of genotypes across environments. However, no single method can adequately explain cultivar performance across environments (Dia et al., 2018). The AMMI model can efficiently interpret GEI as it splits main and interaction effects (Gauch, 2006). It has proved to be a powerful tool to determine the magnitude of GEI for identifying stable and adaptable genotypes (Crossa, 1990). Therefore, Neisse et al. (2018) suggested that the AMMI model was efficient to analyze MET data. However, the AMMI1 biplot is ineffective to identify the discriminating ability and representativeness of environments in METs. Therefore, Yan et al. (2000) endorsed the proposal of Gabriel (1971), who used the biplot technique to display the genotype main effect plus GEI (G+GE) using METs data and called it the GGE biplot. GGE biplot is a graphical tool that displays, interprets and explores two important sources of variation, namely genotype main effect and GE interaction of MET data (Fan et al., 2007; Dyulgerova and Dyulgerov, 2019).
Several univariate parameters have been developed since the 1960s which are still in practice to explain complex patterns of GEI. Among them, the most widely used stability parameters are a deviation from regression (S2di) proposed by Eberhart and Russel (1966), coefficient of determination (Ri2) Pinthus (1973), Wricke’secovalence (Wi) (1962), Perkins and Jinks (1968) proposed Bi and DJi values. Similarly, Lin and Binns (1988) developed a new stability parameter (Pi) based on unpredictable environment variance (year) of genotypic means averaged across a predictable environment (location). The reliability of a model in selecting suitable genotypes has always been a concern of researchers. The AMMI stability value (ASV) is one of the recently developed techniques to measure the stability of genotypes across environments. The ASV developed by Purchase et al. (2000) is the measure of distance from the origin in AMMI2 biplot using scores of PC1 and PC2 of AMMI analysis. The objectives of this study were to; i) assess and compare fitness of different stability models, and ii) identify high yielding and stable wheat lines based on various stability models.
Materials and Methods
Description of experimental sites
Eighty-one wheat genotypes including 79 F5:8 recombinant inbred lines (RILs) and two check cultivars “Janbaz” and “Atta-Habib” were evaluated in nine environments during 2013-16. During 2013-14, the experimental material was planted at single location i.e. The University of Agriculture Peshawar (E-01) for evaluation and seed multiplication, whereas, during 2014-16 at the University of Agriculture Peshawar (E-02 and E-03, respectively), Cereal Crops Research Institute, Pirsabak Nowshehra (E-04 and E-05, respectively), Agricultural Research Station, Swabi (E-06 and E-07, respectively) Agricultural Research Station, Charsadda (E-08 and E-09, respectively). Hereafter, these will be referred to as E-01, E-02, E-03, E-04, E-05, E-06, E-07, E-08, and E-09. Agro-metrological features of test sites/environments including temperature, rainfall, and altitude, etc. are given in Table 1.
Experimental design and procedure
Experimental material was planted in a 9×9 alpha lattice design with two replicates at each environment. Each plot had 6 rows of 5-meter length and a row-to-row space of 30 cm. The standard dose of nitrogen (120 kg ha-1) and phosphorous (80 kg ha-1) was applied using broadcast method. Uniform cultural practices i.e. weeding, roughing etc. required for wheat crops were followed throughout the growing season.
Statistical analysis
Data on grain yield were subjected to Analysis of variance (ANOVA) technique using SAS (SAS, 2009) computer software. Upon significant genotype by environment interaction, grain yield data were further subjected to various stability models i.e. AMMI model, GGE biplot and stability parameters using GEA-R version 4.0 computer software (Pacheco et al., 2018).
Results and Discussion
First two principal components of AMMI model for grain yield captured 54.8% of GEI sum of squares, while the first two principal components of GGE biplot analysis cumulatively explained 54.8% of variation caused by GE interaction (Figure 1, 2). The cumulative PCA scores of both models were the same, providing a uniform condition for selecting appropriate genotype with respect to stability. Eberhart and Russell’s model identified G-79 as a widely stable genotype, whereas genotypes G-17 and G-21 were identified as the stable than other genotypes (Figure 3). Coefficient of variation (CV) declared G-79, G-08, and G-56 as highly productive stable genotypes (Figure 4). Although the cumulative PC scores of both AMMI and GGE model were similar, none of the genotypes was unanimously declared as stable by both models. However, Eberhart and Russell’s model and Francis coefficient of variation identified G-79 as a widely adapted stable genotype.
Based on mean grain yield, G-79 was identified as a top-ranked wheatgenotype, followed by G-08, G-56, G-37, and G-19. The AMMI stability value (ASV) found G-14, G-81, G-52, G-32, and G-28 as more stable wheat genotypes, whereas, coefficient of determination (R2i) revealed G-04, G-38, G-57, G-60 and G-63 as top-ranked genotypes for grain yield. Similarly, Francis coefficient of variation (CV) and cultivar superiority measure (Pi) declared G-79 as top-ranked genotype while Shukla stability value (σi2) and Wrick’s ecovalence (Wi) confirmed G-80 (check cultivar Janbaz), G-52 and G-79 as leading wheat genotypes based on grain yield performance (Table 3).
Table 1: Description of nine environments used for evaluation of 81 wheat during 2014-2016 cropping season.
Environments | Growing season | Geographical positon | Altitude (m.a.s.l) | Average rainfall (mm) |
Temperature (0c) |
||
Latitude | Longitude | Min. | Max. | ||||
E1 | 2014 (AUP) | 34.0150° N | 71.5805° E | 359 | 238 | 20.1 | 34.8 |
E2 | 2015 (AUP) | --do-- | --do-- | --do-- | 415 | 19.5 | 35.4 |
E3 | 2016 (AUP) | --do-- | --do-- | --do-- | 189 | 17.8 | 38.2 |
E4 | 2015 (CCRI) | 34.0159° N | 71.9755° E | 288 | 220 | 10.1 | 28.6 |
E5 | 2016 (CCRI) | --do-- | --do-- | --do-- | 112 | 16.3 | 35.9 |
E6 | 2015 (ARSS) | 34.1442° N | 72.3785° E | 321 | 263 | 18.0 | 36.7 |
E7 | 2016 (ARSS) | --do-- | --do-- | --do-- | 312 | 14.5 | 32.1 |
E8 | 2015 (ARSC) | 34.1494° N | 71.7428° E | 381 | 460 | 10.4 | 28.5 |
E9 | 2016 (ARSC) | --do-- | --do-- | --do-- | 392 | 17.4 | 36.2 |
Table 2: List of wheat RILs with pedigree.
Code | Pedigree | Code | Pedigree |
G-01 | Takbir × Khatakwal-3-1 | G-42 | Tatara × Inqilab-26-7 |
G-02 | Takbir × Khatakwal-3-5 | G-43 | Tatara × Inqilab-26-11 |
G-03 | Takbir × Khatakwal-3-7 | G-44 | Tatara × Inqilab-26-15 |
G-04 | Takbir × Khatakwal-3-8 | G-45 | Tatara × Inqilab-26-20 |
G-05 | Takbir × Khatakwal-3-9 | G-46 | Tatara × Ghaznavi 98-31-1 |
G-06 | Takbir × Khatakwal-3-16 | G-47 | Tatara × Ghaznavi 98-31-2 |
G-07 | Takbir × Khatakwal-3-18 | G-48 | Tatara × Ghaznavi 98-31-4 |
G-08 | Tatara × Inqilab-4-3 | G-49 | Tatara × Ghaznavi 98-31-7 |
G-09 | Tatara × Inqilab-4-6 | G-50 | Ghaznavi 98 × Khatakwal -33-5 |
G-10 | Tatara × Inqilab-4-9 | G-51 | Ghaznavi 98 × Khatakwal -33-7 |
G-11 | Tatara × Inqilab-4-10 | G-52 | Ghaznavi 98 × Khatakwal -33-10 |
G-12 | Tatara × Inqilab-4-11 | G-53 | Ghaznavi 98 × Khatakwal -33-15 |
G-13 | Tatara × Inqilab-4-13 | G-54 | Tatara × Ghaznavi 98-37-15 |
G-14 | Tatara × Inqilab-4-16 | G-55 | Tatara × Margala-43-2 |
G-15 | Wafaq × Ghaznavi 98 | G-56 | Tatara × Margala-43-4 |
G-16 | Wafaq × Ghaznavi 98 | G-57 | Tatara × Margala-43-11 |
G-17 | Wafaq × Ghaznavi 98 | G-58 | Tatara × Margala-43-12 |
G-18 | Tatara × Takbir-9-8 | G-59 | Tatara × Inqilab -45-10 |
G-19 | Tatara × Takbir-9-10 | G-60 | Takbir × Inqilab -45-12 |
G-20 | Tatara × Takbir-9-12 | G-61 | Tatara × Ghaznavi 98-48-2 |
G-21 | Tatara × Takbir-9-813 | G-62 | Tatara × Ghaznavi 98-48-3 |
G-22 | Tatara × Inqilab-18-15 | G-63 | Tatara × Ghaznavi 98-48-13 |
G-23 | Tatara × Inqilab-18-19 | G-64 | Tatara × Ghaznavi 98-48-15 |
G-24 | Tatara × Inqilab-18-20 | G-65 | Tatara × Ghaznavi 98-48-19 |
G-25 | Tatara × Takbir-19-3 | G-66 | Wafaq × Ghaznavi 98-49-2 |
G-26 | Tatara × Takbir-19-4 | G-67 | Wafaq × Ghaznavi 98-49-4 |
G-27 | Tatara × Takbir-19-8 | G-68 | Wafaq × Ghaznavi 98-49-5 |
G-28 | Tatara × Takbir-19-11 | G-69 | Wafaq × Ghaznavi 98-49-6 |
G-29 | Tatara × Takbir-19-16 | G-70 | Wafaq × Ghaznavi 98-49-9 |
G-30 | Tatara × Takbir-19-18 | G-71 | Wafaq × Ghaznavi 98-49-10 |
G-31 | Tatara × Ghaznavi 98-22-1 | G-72 | Wafaq × Ghaznavi 98-49-12 |
G-32 | Tatara × Ghaznavi 98-22-2 | G-73 | Wafaq × Ghaznavi 98-49-13 |
G-33 | Tatara × Ghaznavi 98-22-6 | G-74 | Wafaq × Ghaznavi 98-49-15 |
G-34 | Tatara × Ghaznavi 98-22-8 | G-75 | Wafaq × Ghaznavi 98-49-16 |
G-35 | Tatara × Ghaznavi 98-22-9 | G-76 | Wafaq × Ghaznavi 98-49-19 |
G-36 | Tatara × Ghaznavi 98-22-12 | G-77 | Wafaq × Ghaznavi 98-49-20 |
G-37 | Tatara × Ghaznavi 98-22-13 | G-78 | Tatara × Takbir-19-17 |
G-38 | Tatara × Ghaznavi 98-22-19 | G-79 | Tatara × Takbir-19-18 |
G-39 | Tatara × Ghaznavi 98-22-20 | Check | Janbaz |
G-40 | Tatara × Inqilab-26-4 | Check | Atta-Habib |
G-41 | Tatara × Inqilab-26-6 |
Table 3: Mean ranking of genotypes for grain yield using various stability parameters.
Genotype | Mean | Mean rank | ASV |
R2i |
CV |
σi2 |
Wi |
Pi |
Genotype | Mean | Mean rank | ASV |
R2i |
CV |
σi2 |
Wi |
Pi |
G-01 | 3581 | 22 | 18 | 27 | 14 | 07 | 07 | 15 | G-42 | 3207 | 68 | 43 | 19 | 60 | 42 | 42 | 65 |
G-02 | 3378 | 42 | 40 | 30 | 43 | 31 | 31 | 36 | G-43 | 3588 | 21 | 68 | 74 | 34 | 57 | 57 | 23 |
G-03 | 3441 | 33 | 77 | 79 | 78 | 81 | 81 | 60 | G-44 | 3156 | 71 | 64 | 22 | 72 | 54 | 54 | 74 |
G-04 | 3239 | 65 | 26 | 01 | 55 | 24 | 24 | 61 | G-45 | 3612 | 17 | 09 | 68 | 18 | 29 | 29 | 17 |
G-05 | 3844 | 07 | 54 | 48 | 26 | 64 | 64 | 07 | G-46 | 3490 | 29 | 59 | 31 | 42 | 39 | 39 | 28 |
G-06 | 3405 | 37 | 65 | 69 | 49 | 58 | 58 | 32 | G-47 | 3111 | 76 | 31 | 13 | 50 | 22 | 22 | 76 |
G-07 | 3715 | 11 | 08 | 08 | 20 | 08 | 08 | 10 | G-48 | 3391 | 40 | 58 | 45 | 39 | 43 | 43 | 35 |
G-08 | 4195 | 02 | 72 | 76 | 37 | 70 | 70 | 02 | G-49 | 3356 | 47 | 52 | 32 | 77 | 66 | 66 | 55 |
G-09 | 3264 | 59 | 33 | 06 | 75 | 52 | 52 | 66 | G-50 | 3506 | 27 | 22 | 66 | 02 | 04 | 04 | 21 |
G-10 | 3812 | 08 | 44 | 75 | 15 | 30 | 30 | 06 | G-51 | 3134 | 73 | 81 | 49 | 81 | 79 | 79 | 79 |
G-11 | 3054 | 79 | 07 | 54 | 45 | 40 | 40 | 78 | G-52 | 3315 | 51 | 03 | 15 | 05 | 02 | 02 | 38 |
G-12 | 3138 | 72 | 28 | 41 | 35 | 23 | 23 | 69 | G-53 | 3296 | 54 | 17 | 62 | 16 | 19 | 19 | 46 |
G-13 | 3281 | 57 | 45 | 51 | 36 | 36 | 36 | 56 | G-54 | 3623 | 15 | 71 | 72 | 54 | 73 | 73 | 26 |
G-14 | 3284 | 56 | 01 | 81 | 21 | 32 | 32 | 50 | G-55 | 3389 | 41 | 49 | 12 | 69 | 56 | 56 | 47 |
G-15 | 3354 | 48 | 11 | 23 | 23 | 12 | 12 | 39 | G-56 | 4030 | 03 | 57 | 60 | 10 | 49 | 49 | 03 |
G-16 | 3692 | 13 | 67 | 21 | 40 | 75 | 75 | 20 | G-57 | 3105 | 77 | 30 | 03 | 41 | 13 | 13 | 75 |
G-17 | 3222 | 67 | 21 | 14 | 29 | 09 | 09 | 59 | G-58 | 3392 | 39 | 14 | 39 | 19 | 17 | 17 | 30 |
G-18 | 3400 | 38 | 56 | 61 | 53 | 61 | 61 | 43 | G-59 | 3459 | 32 | 66 | 35 | 65 | 60 | 60 | 31 |
G-19 | 3901 | 05 | 78 | 57 | 47 | 76 | 76 | 09 | G-60 | 3366 | 44 | 69 | 04 | 73 | 55 | 55 | 53 |
G-20 | 3131 | 74 | 25 | 10 | 58 | 27 | 27 | 71 | G-61 | 3241 | 62 | 70 | 09 | 79 | 69 | 69 | 72 |
G-21 | 2873 | 80 | 13 | 18 | 46 | 15 | 15 | 80 | G-62 | 3419 | 35 | 48 | 58 | 38 | 63 | 63 | 37 |
G-22 | 3251 | 61 | 42 | 56 | 44 | 46 | 46 | 62 | G-63 | 3264 | 60 | 61 | 05 | 68 | 50 | 50 | 63 |
G-23 | 3362 | 45 | 76 | 73 | 67 | 74 | 74 | 52 | G-64 | 3544 | 26 | 23 | 25 | 30 | 20 | 20 | 24 |
G-24 | 3325 | 50 | 20 | 64 | 03 | 11 | 11 | 40 | G-65 | 3179 | 70 | 62 | 20 | 59 | 41 | 41 | 70 |
G-25 | 3589 | 20 | 73 | 77 | 63 | 72 | 72 | 27 | G-66 | 3693 | 12 | 19 | 71 | 24 | 47 | 47 | 13 |
G-26 | 3590 | 19 | 16 | 16 | 33 | 21 | 21 | 18 | G-67 | 3101 | 78 | 27 | 38 | 76 | 62 | 62 | 77 |
G-27 | 3467 | 31 | 46 | 26 | 52 | 48 | 48 | 29 | G-68 | 3429 | 34 | 75 | 52 | 71 | 71 | 71 | 44 |
G-28 | 3608 | 18 | 05 | 43 | 28 | 28 | 28 | 16 | G-69 | 3116 | 75 | 41 | 11 | 57 | 25 | 25 | 73 |
G-29 | 3274 | 58 | 34 | 46 | 11 | 10 | 10 | 48 | G-70 | 3678 | 14 | 12 | 67 | 06 | 16 | 16 | 11 |
G-30 | 3481 | 30 | 79 | 44 | 62 | 78 | 78 | 34 | G-71 | 3767 | 09 | 51 | 70 | 48 | 68 | 68 | 12 |
G-31 | 3556 | 23 | 37 | 47 | 31 | 34 | 34 | 25 | G-72 | 3554 | 24 | 36 | 50 | 12 | 18 | 18 | 22 |
G-32 | 3548 | 25 | 04 | 37 | 07 | 06 | 06 | 19 | G-73 | 3873 | 06 | 55 | 42 | 25 | 65 | 65 | 05 |
G-33 | 3409 | 36 | 53 | 53 | 64 | 77 | 77 | 49 | G-74 | 3349 | 49 | 32 | 55 | 08 | 26 | 26 | 33 |
G-34 | 3358 | 46 | 10 | 80 | 27 | 44 | 44 | 41 | G-75 | 3366 | 43 | 38 | 63 | 32 | 51 | 51 | 45 |
G-35 | 3615 | 16 | 35 | 33 | 17 | 14 | 14 | 14 | G-76 | 3225 | 66 | 60 | 28 | 51 | 37 | 37 | 64 |
G-36 | 3756 | 10 | 29 | 78 | 13 | 33 | 33 | 08 | G-77 | 3240 | 63 | 50 | 59 | 61 | 59 | 59 | 67 |
G-37 | 4003 | 04 | 74 | 36 | 22 | 67 | 67 | 04 | G-78 | 3206 | 69 | 63 | 07 | 66 | 38 | 38 | 68 |
G-38 | 3314 | 53 | 47 | 02 | 74 | 53 | 53 | 58 | G-79 | 4862 | 01 | 06 | 65 | 01 | 03 | 03 | 01 |
G-39 | 3315 | 52 | 24 | 29 | 56 | 45 | 45 | 51 | G-80 | 3287 | 55 | 15 | 24 | 04 | 01 | 01 | 42 |
G-40 | 2804 | 81 | 39 | 17 | 70 | 35 | 35 | 81 | G-81 | 3240 | 64 | 02 | 34 | 09 | 05 | 05 | 57 |
G-41 | 3497 | 28 | 80 | 40 | 80 | 80 | 80 | 54 |
AMMI stability value (ASV); Coefficient of determination (Ri2); Francis coefficient of variation (CV); Shukla variance (σi2); Wricke’s ecovalence value (Wi) and Lin and Binns model (Pi).
Spearman’s rank correlation coefficient analysis indicated that Ri2 had significantly positive correlations with mean grain yield and significantly negative with yield ranking (0.47 vs -0.47). The relationship of Ri2with mean performance and yield ranking of wheat genotypes for grain yield indicated that the ranking of genotypes was not similar as calculated by Ri2 and mean performance. Furthermore, Pi exhibited significantly positive correlations with yield ranking and significantly negative with mean grain yield (0.96 vs -0.96). The relationship of Pi with mean performance and yield ranking of wheat genotypes for grain yield indicated that the ranking of genotypes was almost similar as calculated by Pi and mean performance. Moreover, the rest of the stability parameters displayed non-significant correlations with both mean and ranking of the genotypes for grain yield. The ASV showed significantly positive associations with CV (0.62), σi2 (0.82) and Wi (0.82), inferring that these parameters were same in their abilities to identify stable genotypes (Table 4). The CV exhibited significantly positive correlations with σi2 (0.69), Wi (0.69) and Pi (61). Shukla stability parameter (σi2) expressed a perfect relationship with Wi (1.00), indicating that both parameters had similar results. Positive correlations of ASV with CV, σi2 with Wi, and Wi with CV revealed that these parameters could invariably be used for identifying stable wheat genotypes (Table 4).
Table 4: Spearman ranks correlation coefficient among stability parameter for grain yield in wheat.
Mean | Mean rank | ASV |
R2i |
CV |
σi2 |
Wi |
|
Mean rank |
-1.00** |
||||||
ASV |
0.15 ns |
-0.15 ns |
|||||
R2i |
0.47** |
-0.47** |
0.09 ns |
||||
CV |
-0.30 ns |
0.30 ns |
0.62** |
-0.31 ns |
|||
σi2 |
0.18 ns |
-0.18 ns |
0.82** |
0.25 ns |
0.69** |
||
Wi |
0.18 ns |
-0.18 ns |
0.82** |
0.25 ns |
0.69** |
1.00** |
|
Pi |
-0.95** |
0.95** |
0.04 ns |
-0.45** |
0.60** |
0.04 ns |
0.04 ns |
AMMI stability value (ASV); Coefficient of determination (Ri2); Francis coefficient of variation (CV); Shukla variance (σi2); Wricke’s ecovalence value (Wi) and Lin and Binns model (Pi).
The main purpose of this study was to check the adequacy of various stability models with respect to the findings of the current study. Serious limitations for the analysis of genotype by environment interaction have been identified while using simple ANOVA (Gauch and Zobel, 1988). Moreover, regression and other stability analysis provide less information regarding the performance and classification of steady genotypes in METs (Manrique and Hermann, 2002). Among several statistical methods, AMMI and GGE biplot analyses had been reported to be efficient in explaining the complexity of GE interactions (Malik et al., 2019). Various studies have been carried out to examine the efficiency of AMMI and GGE biplot methods in which different researchers presented different logics to support their viewpoints (Gauch, 2006; Yan et al., 2007; Gauch et al., 2008). They also claimed that AMMI2 was more efficient than GGE, thus summarizing their statement as AMMI2>GGE>AMMI1. This statement has been further validated by the conclusions of this study. Hagos and Abay (2013) suggested that both GGE and AMMI biplots were important for evaluating stable and adaptable genotypes in METs. Similar results were reported by Stojakovic et al. (2010), Mitrovic et al. (2012), Rad et al. (2013) and Tiwari (2019), indicating that AMMI biplot performed equally well as the GGE biplot. Numerical stability parameters had also been identified as a good tool to rank genotypes based on their stability in METs (Sayyed and Mohammadi, 2008; Tamene et al., 2015). Spearman’s rank correlation exhibited that most of the stability parameters had a significantly positive correlation with each other, indicating that these parameters were equally applicable for identifying stable genotypes.
Before jumping into conclusions, this study supports the idea of Yang et al. (2009) that complementary statistical tests should be followed in addition to biplot analysis to ascertain genotypic stability. However, despite some flaws, the usefulness and suitable visualization of GE interaction of these models cannot be surpassed. More critical analyses would open the horizons for further improvement of the weakspots that exist in these models. Soon, it is generally accepted among the scientists that AMMI and GGE biplot analyses would be the ultimate choice to obtain conclusive information from METs. Based on current results, it is recommended that AMMI and GGE biplot analysis should be complemented by the critical review of genotypes stability with multiple stability models to scrutinize wheat genotypesfor wider adaptation.
Conclusions and Recommendations
Graphical stability approaches provided more or less similar results in terms of identifying stable wheat genotypes for grain yield. Different stability models viz. AMMI, GGE biplot, Eberhart and Russell’s model, Francis coefficient of variation (CV) declared the genotype G-79 as top-ranked while Shukla stability value (σi2) and Wrick’s ecovalence (Wi) identified G-80 (check cultivar Janbaz), G-52 and G-79 as leading wheat genotypes based on grain yield. Spearman’s rank correlation revealed significant positive correlations of AMMI stability value (ASV) with CV, σi2 with Wi, and Wi with CV indicating that these parameters could invariably be used for identifying stable wheat genotypes. Different stability models identified G-79 as high yielding and stable genotype and thus could be recommended for commercialization in the province of Khyber Pakhtunkhwa, Pakistan.
Novelty Statement
A high yielding stable wheat genotypes was identified using multiple stability models out of 81 wheat recombinant inbred lines (RIL’s) tested across nine environments during three years.
Author’s Contribution
Malak Atiq Ullah Khan: Conducted the experiments and collected the data.
Fida Mohammad: Designed the experiment.
Fahim Ullah Khan: Wrote the paper.
Sheraz Ahmad: Analyzed the data.
Mian Ahmad Raza: Collected data
Tariq Kamal: Reviewed the paper
Conflict of interest
The authors have declared no conflict of interest.
References
Abraha, M.T., H. Shimelis, T. Solomon and A. Hailu. 2019. Genotype-by-environment interaction and selection of elite wheat genotypes under variable rainfall conditions in northern Ethiopia. J. Crop Improv. pp. 1–17. https://doi.org/10.1080/15427528.2019.1662531
Ain, Q.U., A. Rasheed, A. Anwar, T. Mahmood, M. Imtiaz, T. Mahmood, X. Xia, Z. He and U.M. Quraishi. 2015. Genome-wide association for grain yield under rainfed conditions in historical wheat cultivars from Pakistan. Front. Plant Sci. 6(September): 743. https://doi.org/10.3389/fpls.2015.00743
Crossa, J., G.H. Gauch and R.W. Zobel. 1990. Additive main effects and multiplicative interaction analysis of two international maize cultivar trials. Crop Sci. 30: 493-500. https://doi.org/10.2135/cropsci1990.0011183X003000030003x
Dehghani, H., A. Ebadi and A. Yousefi. 2006. Biplot analysis of genotype by environment interaction for barley yield in Iran. Agron. J. 98: 388-393. https://doi.org/10.2134/agronj2004.0310
Dia, M., T.C. Wehner, G.W. Elmstrom, A. Gabert, J.E. Motes, J.E. Staub, G.E. Tolla and I.E. Widders. 2018. Genotype X environment interaction for yield of pickling cucumber in 24 U.S. Environments. Open Agric. 3(1): 1–16. https://doi.org/10.1515/opag-2018-0001
Dyulgerova, B. and N. Dyulgerov. 2019. Genotype by environment interaction for grain yield of barley mutant lines. Agric. 65(2): 51–58. https://doi.org/10.2478/agri-2019-0006
Eberhart, S.A. and W.A. Russell. 1966. Stability parameter for comparing varieties. Crop Sci. 6: 36-40. https://doi.org/10.2135/cropsci1966.0011183X000600010011x
Fan, X.M., M.S. Kang, H. Chen, Y. Zhang, J. Tan and C. Xu. 2007. Yield stability of maize hybrids evaluated in multi-environment trials in Yunnan, China. Agron. J. 99: 220-228. https://doi.org/10.2134/agronj2006.0144
Finlay, K.W. and G.N. Wilkinson. 1963. The analysis of adaptation in a plant breeding program. Aust. J. Agric. Res. 14: 742-754. https://doi.org/10.1071/AR9630742
Francis, T.R. and L.W. Kannenberg. 1978. Yield stability studies in short-season maize. I.A descriptive method for grouping genotypes. Can. J. Plant Sci. 58: 1029-1034. https://doi.org/10.4141/cjps78-157
Gabriel, K.R., 1971. The biplot graphic display of matrices with application to principal component analysis. Biometrika. 58: 453-467. https://doi.org/10.1093/biomet/58.3.453
Gauch, H.G. and R.W. Zobel. 1997. Identifying mega-environments and targeting genotypes. Crop Sci. 37: 311-326. https://doi.org/10.2135/cropsci1997.0011183X003700020002x
Gauch, H.G., H.P. Piepho and P. Annicchiarico. 2008. Statistical analysis of yield trials by AMMI and GGE. Further considerations. Crop Sci. 48: 866-889. https://doi.org/10.2135/cropsci2007.09.0513
Gauch, H.G., 2006. Statistical analysis of yield trials by AMMI and GGE. Crop Sci. 46: 1488-1500. https://doi.org/10.2135/cropsci2005.07-0193
Gauch, H.G. and R.W. Zobel. 1988. Predictive and postdictive success of statistical analysis of yield trial. Theo. App. Genet. 76: 1-10. https://doi.org/10.1007/BF00288824
Gauch, H.G. and R.W. Zobel. 1996. AMMI analysis of yield trials. In: Kang, M.S., Gauch, H.G. (ed.) Genotype by environment interaction. CRC Press, Boca Raton, FL. https://doi.org/10.1201/9781420049374.ch4
Gruneberg, W.J., K. Manrique, D. Zhang and M. Hermann. 2006. Genotype × environment interactions for a diverse set of sweet potato clones evaluated across varying ecographic conditions in Peru. Crop Sci. 45: 2160-2171. https://doi.org/10.2135/cropsci2003.0533
Hagos, H.G. and F. Abay. 2013. AMMI and GGE biplot analysis of bread wheat genotypes in the Northern part of Ethiopia. J. Plant Breed. Genet. pp. 12-18.
Lin, C.S. and M.R. Binns. 1988. A superiority measure of cultivar performance for cultivar × location data. Can. J. Plant Sci. 68: 193-198. https://doi.org/10.4141/cjps88-018
Malik, W.A., J. Forkman and H.P. Piepho. 2019. Testing multiplicative terms in AMMI and GGE models for multi-environment trials with replicates. Theor. Appl. Genet. 132(7): 2087–2096. https://doi.org/10.1007/s00122-019-03339-8
Manrique, K. and M. Hermann. 2002. A comparative study to determine stable performance in sweetpotato (Ipomoea batatas [L.] Lam.) Regional trials. Inf. Syst. Div., Nat. Agric. Libr. https://doi.org/10.17660/ActaHortic.2002.583.9
Mitrovic, B., D. Stanisavljevic, S. Treski, M. Stojakovic, M. Ivanovic, G. Bekavac and M. Rajkovic. 2012. Evaluation of experimental maize hybrids tested in multi-location trials using AMMI and GGE biplot analyses. Turk. J. Field Crops. 17: 35-40.
Mohammad. F., O.S. Abdalla, S. Rajaram, A. Yaljarouka, N.U. Khan, A.Z. Khan, S.K. Khalil, I.H. Khalil, I. Ahmad and S.A. Jadoon. 2013. Additive main effect and multiplicative analysis of synthetic-derived wheat under varying moisture regimes. Pak. J. Bot. 43(2): 1205-1210.
Neisse, A.C., J.L. Kirch and K. Hongyu. 2018. AMMI and GGE Biplot for genotype × environment interaction: a medoid–based hierarchical cluster analysis approach for high–dimensional data. Biometrical Lett. 55(2): 97–121. https://doi.org/10.2478/bile-2018-0008
Pacheco, Á., M. Vargas, G. Alvarado, F. Rodríguez, J. Crossa and J. Burgueño. 2018. GEA-R (Genotype × Environment analysis with R for windows) Version 4.1.
Perkins, J.M. and J.L. Jinks. 1968. Environmental and genotype-environmental components of variability III. Multiple lines and crosses. Heredity (Edinb). 23(3): 339–356. https://doi.org/10.1038/hdy.1968.48
Pinthus, M.J., 1973. Estimates of genotypic value: a proposed method. Euphytica, 22: 345-351. https://doi.org/10.1007/BF00021563
Purchase, J.L., H. Hatting and C.S. van Deventer. 2000. Genotype × environment interaction of winter wheat (T. aestivum) in South Africa: Stability analysis of yield performance. S. Afr. J. Plant Soil 17(3): 101-107. https://doi.org/10.1080/02571862.2000.10634878
Rad, N.M., M.A. Kadir, M.Y. Rafii, H.Z. Jaafar, M.R. Naghavi and F. Ahmadi. 2013. Genotype × environment interaction by AMMI and GGE biplot analysis in three consecutive generations of wheat (Triticum aestivum. L) under normal and drought stress conditions. Aust. J. Crop Sci., 7: 956-961.
SAS Institute Inc. 2009. SAS/STAT ® 9.2 User’s Guide, Second Edition. Copyright © 2009, SAS Inst. Inc., Cary, NC, USA. https:// support. sas.com/ documentation/ cdl/en/statug/ 63033/HTML/default/viewer.htm).
Sayyed, S.P. and R. Mohammadi. 2008. Use of stability parameters for comparing safflower genotypes in multi-environment trials. 7th Int. Safflower Conf. Wagga Wagga Aust. https://doi.org/10.3923/ajps.2008.100.104
Shukla, G.K., 1972. Some statistical aspects of portioning genotype–environmental components of variability. Heredity. 29: 237-245. https://doi.org/10.1038/hdy.1972.87
Singh, P.K. and R.D. Choudhary. 1997. Biometrical methods in quantitative genetic analysis. Kalyani Publishers, New Delhi. pp. 178-185.
Stojakovi,c M., M. Ivanovic, D. Jockovic, G. Bekavac, B. Purar, A. Nastasic, D. Stanisavljevic, B. Mitrovic, S. Treskic and R. Laisic. 2010. NS maize hybrids in production regions of Serbia. Field Vegetable Crops Res. 47: 93-102.
Tamene, T., G. Keneni, T. Sefera, and M. Jarso. 2015. Yield stability and relationships among stability parameters in faba bean (Viciafaba L.) genotypes. Crop Sci. Soc. China Inst. Crop Sci., CAAS. Prod. Hosting Elsevier B.V.
Tiwari, J.K., 2019. GGE biplot and AMMI model to evaluate spine gourd (Momordica dioicaRoxb.) for genotype × environment interactionand seasonal adaptation. Electron. J. Plant Breed. 10(1): 264–271. https://doi.org/10.5958/0975-928X.2019.00031.0
Wricke, G., 1962. On a method of understanding the biological diversity in field research. Z. Pfl.-Zücht. 47: 92–96.
Yan, W. and M.S. Kang. 2003. GGE Biplot Analysis: A graphical tool for breeders, geneticists, and agronomists. CRC Press, Boca Raton, F.L. https://doi.org/10.1201/9781420040371
Yan, W. and N.A. Tinker. 2006. Biplot analysis of multi-environment trial data: Principles and applications. Can. J. Plant Sci. 86: 623-645. https://doi.org/10.4141/P05-169
Yan, W., L.A. Hunt, Q. Sheng and Z. Szlavnics. 2000. Cultivar evaluation and mega-environment investigation based on GGE biplot. Crop Sci. 40: 596-605. https://doi.org/10.2135/cropsci2000.403597x
Yan, W., M.S. Kang, B. Ma, S. Woods and P.L. Cornelius. 2007. GGE biplot vs. AMMI analysis of genotype-by-environment data. Crop Sci. 47(2): 643–655. https://doi.org/10.2135/cropsci2006.06.0374
Yang, R.C., J. Crossa, P.L. Cornelius and J. Burgueno. 2009. Biplot analysis of genotype × environment interaction: proceed with caution. Crop Sci. 49: 15641576. https://doi.org/10.2135/cropsci2008.11.0665
Zobel, R.W., M.J. Wright and H.G. Gauch. 1988. Statistical analysis of a yield trial. Agron. J. 80: 388-393. https://doi.org/10.2134/agronj1988.00021962008000030002x
To share on other social networks, click on any share button. What are these?