Identification of Salinity Tolerant Stable Sugarca
Identification of Salinity Tolerant Stable Sugarca
Identification of Salinity Tolerant Stable Sugarca
Abstract: Additive main effects and multiplicative interaction (AMMI), as well as various AMMI-
derived statistics, Genotype, and Genotype × Environment Interaction (GGE) models were em-
ployed on 24 sugarcane genotypes planted during two seasons (2017–18, 2018–19) under different
induced salinity stress environments using saline water irrigation (iw) viz., E1 (Normal iw during
crop season 2017–18), E2 (Normal iw during crop season 2018–19), E3 (4 dsm−1 ECiw during crop sea-
son 2017–18), E4 (4 dsm−1 ECiw during crop season 2018–19), E5 (8 dsm−1 ECiw during crop season
2017–18), E6 (8 dsm−1 ECiw during crop season 2018–19), E7 (12 dsm−1 ECiw during crop season 2017–
18) and E8 (12 dsm−1 ECiw during crop season 2018–19) to assess the genotype by the environment
interaction for the cane yield, commercial cane sugar (CCS) yield, number of millable cane (NMC),
single cane weight (SCW), and pol % in juice. Individual and interactive effects of the genotype and
environment for all the traits were significant. In the expression of total variability, the environmen-
tal contribution was higher for the cane yield (66.98%), CCS yield (67.60%), NMC (65.78%), and SCW
(43.27%), whereas genotypic contribution was higher in the expression of pol% (82.48%). As per
Citation: Kumar, R.; Dhansu, P.;
AMMI Stability Value (ASV), G14 (Co 13033), G23 (Co 15026), G7 (Co 05009), G17 (Co 13036), and
Kulshreshtha, N.; Meena, M.R.;
G2 (Co 15025) were the most stable genotypes for the cane yield. Whereas as per GSI (genotype
Kumaraswamy, M.H.; Appunu, C.;
selection index), genotypes G24 (Co 15027), G21 (Co 15023), G23 (Co 15026), and G17 (Co 13036)
Chhabra, M.L.; Pandey, S.K.
Identification of Salinity Tolerant
were found most stable. The Sustainability Index (SI) of the cane yield (CY) and its contributing and
Stable Sugarcane Cultivars Using CY-based computed traits were low for most of the genotypes, which indicates the negative impact
AMMI, GGE and Some Other of increased levels of irrigation-induced salinity in the expression of these traits. In the mean vs
Stability Parameters Under Multi stability biplot analysis, G21 (Co 15023), G24 (Co 15027), G16 (Co 13036), G6 (Co 0238), and G20 (Co
Environments of Salinity Stress. 14036) were found to be highly productive and stable genotypes for the cane yield. The superior
Sustainability 2023, 15, 1119. and stable performance of early maturing notified varieties G21 (Co 15023) and G6 (Co 0238) for CY
https://doi.org/10.3390/su15021119 and CCS yield indicates that they will help the farmers to obtain sustainable income in saline soil
Academic Editor: Jun-Ichi Sakagami conditions.
1. Introduction
Copyright: © 2023 by the authors. Li-
censee MDPI, Basel, Switzerland. Sugarcane, being a C4 crop, thrives well in tropical environments but is cultivated
This article is an open access article globally under varied climatic conditions of tropical and sub-tropical regions [1]. In the
distributed under the terms and con- recent past, Indian sugarcane agriculture had witnessed a swift improvement in cane and
ditions of the Creative Commons At- sugar production. India is the second largest sugarcane producer after Brazil, with around
tribution (CC BY) license (https://cre- 4.79 m ha area, 370.5 mt production, and 77.35 t ha−1 productivity [2]. Sugarcane has the
ativecommons.org/licenses/by/4.0/). ability to survive against various environmental-related limiting factors [3–6]. The
theoretical maximum cane yield for sugarcane is 472 t ha−1 [7], but various environmental
(biotic and abiotic) and agronomic factors (crop geometry, planting time, crop duration,
rotation, water, weeds, diseases, pests and nutrients management practices, crop lodging
etc.) limit the crop yield. Soil salinity is significantly coercing crop productivity, predom-
inantly in arid and semiarid regions. In India, the great Indogangetic plane (Punjab, Har-
yana, Uttar Pradesh, Bihar, and some parts of Rajasthan), arid tracts of Gujarat and Raja-
sthan and semi-arid tracts of Gujarat, Madhya Pradesh, Maharashtra, Karnataka, and An-
dhra Pradesh are largely affected by soil salinity [8]. Five states [Gujarat (2.23 m ha),
Uttar Pradesh (1.37 m ha), Maharashtra (0.61 m ha), West Bengal (0.44 m ha) and Raja-
sthan (0.38 m ha)] together account for almost 75% of the saline and sodic soils; further-
more, the area under salt-affected soils is estimated to be tripled (20 million ha) in India
by 2050 [9]. The problem of fringe quality water also befalls the northwestern arid part of
India, especially in the states of Rajasthan, Haryana, and Punjab [10]. Salinity inhibits
plant growth through ion toxicity, nutritional imbalances, osmotic effect, and oxidative
stress [11–13]. Although sugarcane is pondered as moderately sensitive against salinity
stress [14,15], the prolonged stay of the crop (one plant + one or two ratoon crops) in the
salt-affected area greatly limits the sugarcane yield [15,16]. The ill effect of salinity on the
growth, development, and yield contributing traits of sugarcane have been reported by
several researchers [17–21]-. Rao et al. [22] in their study identified the threshold value for
sugarcane under salinity as 1.7 dSm−1 and suggested that yield decreases by 5.9% with a
per unit increase in salinity. Irrigation-induced salinity or sodicity in sugarcane is reported
in several countries viz., Australia, Egypt, Iraq, the United States, India, Pakistan, Swazi-
land, South Africa, and Zimbabwe [23–25]. Increased soil salinity or sodicity are the most
substantial soil chemical processes which lead to soil degradation under irrigated sugar-
cane [26]. The resistant and susceptible sugarcane genotypes express differential re-
sponses for various growth and yield traits against dissimilar salinity levels [27–31]. It
indicates that there is a need to study the interaction effects of genotype, environment,
and G × E thoroughly against different levels of salinity [5,32]. Plant breeders overcome
the GEI (genotype by environment interaction) challenges by evaluating genotypes in a
variety of distinct environments to ensure that the specific genotype with a high yield and
stable performance is selected [4]. Stable performance and better adaptability are the main
criteria for the selection of genotypes in any breeding program [33]. Environment plays a
dominant role in the expression of the cane yield and attributed traits in sugarcane, and
the importance of G × E interaction is widely recognized [34–37]. The two widely used
biplot models are the AMMI biplot (the additive main effects and multiplicative interac-
tion and the GGE biplot (genotype + genotype × environment). The analysis of variance
of the genotype and environment main effects with the PCA of the GEI generates the
AMMI model, whereas the AMMI2 or GEI biplot is performed based on the singular value
decomposition (SVD) of a double centered G×E table [38]. The GGE biplots are based on
the environment-centered SVD, provided by Yan et al. [39] and graphically represent both
the genotype and genotype-by-environment based on the primary sources of variation
associated with the genotype assessment. The AMMI technique is effective in identifying
the discriminating genotypes that had stable performance across diverse environmental
conditions [40,41]. During yield trials, an additive main effect and a multiplicative inter-
action (AMMI) model are widely used to analyze G × E interaction [42]. AMMI is capable
of detecting GEI in a multi-dimensional environment and displaying it using a biplot.
GGE biplots-based multi-environment trail, genotype evaluation, and environmental val-
uation have been successfully executed for varietal stability analysis by several research-
ers [43-48]. The GGE biplot approach for decomposing genotype plus genotype-by-envi-
ronment (G + G × E) is more effective in a biplot graph compared with AMMI analysis. In
addition, the GGE biplot analysis has been used by several researchers to classify the mega
environment, assess genotype rankings, and decide the discriminative and representative
among the tested environments [42]. The GGE biplot will aid researchers in better under-
standing complicated GE interactions in multi-environment breeding line trials and
Sustainability 2023, 15, 1119 3 of 19
agronomic investigations [45]. The GGE biplot was used to determine the performance of
crop cultivars in a variety of stress conditions, ideal cultivars, mega-environment, and
core testing sites [49]. The direct presentation of genotype effects is not feasible in AMMI2
biplots since this approach only decomposes G × E interaction effects in the PCA. GGE
biplot analysis, on the other hand, is regarded as a useful statistical technique for produc-
ing phenotypically stable and superior cultivars, identifying stable genotypes across sev-
eral environments and achieving crop yield stability across multiple locations.
The AMMI model does not provide a quantitative stability measure, which is essen-
tial to quantify and rank the genotypes in terms of yield stability [50]. The AMMI stability
value (ASV) is used as a selection criterion to quantify and rank the genotypes according
to their yield stability [51]. Further stability per se should not be the only selection criteria,
because the most stable genotypes may not necessarily give the best yield performance
[34, 35]. Therefore, various authors have introduced different selection criteria for the sim-
ulation selection of yield and stability [52-58]. Therefore, the present study aims to identify
superior genotypes with stable yield performance over different salinity stress environ-
ments by evaluating the efficacy of various stability analysis methodologies.
package and practices. In the two consequent years, a total of eight induced production
environments of irrigation water salinity viz., E1 (Niw during crop season 2017–18), E2
(Niw during crop season 2018–19), E3 (4 dsm−1ECiw during crop season 2017–18), E4 (4
dsm−1ECiw during crop season 2018–19), E5 (8 dsm−1ECiw during crop season 2017–18), E6
(8 dsm−1ECiw during crop season 2018–19), E7 (12 dsm−1ECiw during crop season 2017–18),
and E8 (12 dsm−1ECiw during crop season 2018–19) were developed in the ring pits.
𝑆𝑆𝐼𝑃𝐶𝐴1
𝐴𝑆𝑉 = √[( ) × (𝐼𝑃𝐶𝐴1𝑠𝑐𝑜𝑟𝑒 )] + (𝐼𝑃𝐶𝐴2𝑠𝑐𝑜𝑟𝑒 )2
𝑆𝑆𝐼𝑃𝐶𝐴2
where SSIPCA1/SSIPCA2 is the weight given to the IPCA1-value by dividing the IPCA1 sum of
squares by the IPCA2 sum of squares. The larger the IPCA score, either negative or posi-
tive, the more specifically adapted a genotype is to certain environments. Smaller ASV
scores indicate a more stable genotype across environments.
𝑌 − 𝜎𝑛
𝑆𝐼 = [ ] × 100
𝑌𝑀
where Y = Average performance of a genotype, σn = Standard deviation, and YM = Best
performance of a genotype in any environment. The values of the sustainability index
were divided arbitrarily into five groups viz. very low (up to 20%), low (21–40%), moder-
ate (41–60%), high (61–80%), and very high (above 80%).
3. Results
3.1. Effect of Salinity on Sugarcane Genotypes—AMMI Analysis
The analysis of variance (ANOVA) showed that individual and interactive effects of
Genotypes (G), Environments (E), and genotype × environment interaction (G × E) were
significant for all the studied traits viz., the cane yield, CCS yield, NMC population, SCW
and Pol%. The environmental main effect represented 66.98%, the genotype explained
25.41%, and the G × E interaction explained 7.61% of the total variation for the cane yield.
Similarly for the CCS yield (t ha−1), the contribution of environment, genotype, and inter-
action effects on the total variation was 67.60%, 24.88%, and 8.12%, respectively. In addi-
tion, significant variations for NMC (represented 65.78% environmental variation, 21.81%
genotypic variation and 12.41 % G × E variation) were also observed. The analysis of var-
iance revealed 43.27% environmental variation, 42.74% genotypic variation, and 13.99 %
G × E variation for SCW (Table 1). For pol% (sucrose% in juice), the analysis of variance
revealed the presence of a highly significant variation for genotype (82.48%), environment
main effect (9.45%), and moderate interaction effects (8.07%).
Table 1. Analysis of variance of main effects and interactions for Cane yield, CCS t ha−1, NMC, SCW
and Pol % and variability explained in percent.
Cane Yield ha−1 CCS t ha−1 NMC ‘000 no. ha−1 SCW (kg) Pol%
Source df
M.S. VE (%) M.S. VE (%) M.S. VE (%) M.S. VE (%) M.S. VE (%)
Genotypes 23 4453.61 ** 25.41 68.57 ** 24.88 1413.3 ** 21.81 0.75 ** 42.74 45.60 ** 82.48
Environments 7 38,571.59 ** 66.98 627.28 ** 67.60 14,003.6 ** 65.78 2.48 ** 43.27 17.17 ** 9.45
Interactions 161 190.48 ** 7.61 8.12 ** 8.12 114.9 ** 12.41 0.03 ** 13.99 0.64 * 8.07
IPCA1 29 605.88 ** 57.29 11.84 ** 65.10 320.5 ** 50.25 0.11 ** 54.51 1.88 ** 53.02
IPCA2 27 224.25 ** 19.74 3.23 ** 16.52 157.0 ** 22.91 0.06 ** 27.55 0.87 ** 22.02
IPCA3 25 148.54 ** 12.10 2.00 ** 9.48 125.1 ** 16.91 0.03 ** 12.15 0.46 ns 11.25
IPCA4 23 113.50 ** 8.51 1.46 ** 6.34 65.2 ** 8.10 0.01 * 3.77 0.22 ns 5.97
Residuals 384 22.16 ns 00 0.46 ns 00 15.18 ns 00 0.002 ns 00 0.49 ns 00
Note: df = degree of freedom, M.S = Mean sum of square, VE% = variability explained %, *, ** and
*** indicates 5%, 1% and 0.1% level of significance, ns = non significance.
The difference between the principal components (IPCA) values was also highly sig-
nificant, and the first two components accounted for 77.03% of the whole effect on the
variation of the cane yield, 81.62% for CCS t ha−1, 73.16% for NMC (thousand ha−1), 82.06%
for SCW (kg), and 75.04% for Pol% (Table 1).
3.1.1. Biplot Analysis for Determination of Main Effect and Environment Influence
PC1 (principle component 1) Vs CY (Cane yield) environments E5, E6, E7, and E8
[higher ECiw 8 (E5, E6) and ECiw 12 (E7, E8)] demonstrated lower average main effects,
whereas environments E1, E2 (Normal ECiw), expressed the highest main effects and were
gainful for most of the genotypes. The PC1 scores for environments E3 and E4 (4 EC iw) are
near zero. Genotypes G20, G24, G21, G6, G4, G13, G8, G13, and G15, expressed higher
main effects; for the cane yield, on the contrary, genotypes G12, G2, G10, G19, G1, and
G18 exhibited lower main effects. (Figure 1a). The AMMI biplot using PC1 and PC2 scores
Sustainability 2023, 15, 1119 6 of 19
for the cane yield is displayed in Figure 1b. Genotypes G23, G24, G6, G14, G3, G21, and
G20 are stable near the origin, hence they have better adaptation across the environments.
(a)
(b)
Figure 1. (a). AMMI biplot PC1 Vs Cane Yield (CY); (b). AMMI Biplot PC1 Vs PC2 for Cane yield (t
ha−1); Where G = Genotypes (1–24) and E = Environments (1–8) of different ECiw levels viz., Normal
(E1, E2), 4EC (E3, E4), 8EC (E5, E6) and 12 EC (E7, E8).
The AMMI biplot for CCS yield drawn using PC Vs CCSY (Figure 2a) and PC1 Vs
PC2 (Figure 2b) indicates E1, E2, E3, and E4 as the favorable environments, whereas E5,
E6, E7, and E8 as poor environments. Similarly, G21, G24, G4, G6, G13, and G20 are rated
as the better performer genotypes for the trait, while G1, G2, G10, and G12 are rated as
the poor performer genotypes. Genotypes G24, G21, and G16 are located near the origin
in the PC1 Vs PC2 biplot and are stable performers (Figure 2b).
Sustainability 2023, 15, 1119 7 of 19
(a)
(b)
Figure 2. (a). AMMI biplot PC1 Vs CCS Yield (CCSY); (b). AMMI Biplot PC1 Vs PC2 for CCS yield
(t ha−1); Where G = Genotypes (1–24) and E = Environments (1–8) of different ECiw levels viz., Normal
(E1, E2), 4EC (E3, E4), 8EC (E5, E6) and 12 EC (E7, E8).
13035) for Pol%, were the most stable genotypes for respective traits. On the contrary, G12
(Co 12027), G2 (CoS 767), G4 (Co 0118) for cane yield; G9(Co 06034), G11 (Co 12026), G8
(Co 05011) for CCS yield; G9 (Co 06034), G11 (Co 12026), G8 (Co 05011) for NMC; G5 (Co
0237), G22 (Co 15025), G1 (Co 1148) for SCW and G6 (Co 0238), G5 (Co 0237), and G4 (Co
0118) for pol% due to highest ASV ranks found most unstable for the respective traits.
Table 2. Average values of observed traits for genotypes, AMMI stability value (ASV), rank of the ASV (RA), rank of trait mean (RM) and genotype
selection index (GSI).
Clo Cane Yield ha−1 CCS t ha−1 NMC Thousands ha−1 SCW (kg) Pol%
nes Mean ASV RA RM GSI Mean ASV RA RM GSI Mean ASV RA RM GSI Mean ASV RA RM GSI Mean ASV RA RM GSI
G1 57.67 7.78 18 10 28 7.58 4.08 21 12 33 71.57 2.93 13 1 14 0.80 0.66 22 16 38 15.41 0.69 15 21 36
G2 53.55 8.48 23 20 43 5.73 4.31 22 22 44 54.74 2.15 9 16 25 0.75 0.49 18 18 36 15.88 0.22 4 19 23
G3 71.23 2.21 7 14 21 7.97 0.59 4 11 15 65.74 1.97 8 5 13 0.79 0.23 7 17 24 17.16 0.33 7 12 19
G4 37.33 8.24 22 3 25 10.80 5.33 24 3 27 59.68 3.50 16 12 28 1.16 0.23 6 3 9 17.30 1.20 22 9 31
G5 70.60 4.88 14 23 37 6.34 3.72 19 18 37 46.40 4.55 21 23 44 0.73 0.88 24 19 43 18.85 2.29 23 3 26
G6 44.69 4.45 13 5 18 9.83 0.20 1 6 7 60.09 3.49 15 10 25 1.11 0.32 12 4 16 17.00 2.40 24 13 37
G7 61.76 1.18 3 16 19 6.37 0.70 6 17 23 59.94 3.85 18 11 29 0.72 0.31 11 20 31 16.10 1.18 21 17 38
G8 40.33 7.91 19 9 28 8.64 3.26 16 9 25 69.80 5.49 22 2 24 0.83 0.45 16 14 30 16.07 0.88 20 18 38
G9 42.27 3.21 10 21 31 6.32 1.43 11 19 30 54.09 8.34 24 17 41 0.68 0.21 4 23 27 18.13 0.56 10 4 14
G10 39.58 7.47 17 18 35 5.32 4.83 23 23 46 50.91 1.18 5 20 25 0.80 0.44 15 15 30 14.85 0.84 17 22 39
G11 31.54 2.17 6 22 28 5.95 1.18 9 21 30 52.46 6.63 23 18 41 0.69 0.15 2 22 24 17.19 0.58 11 11 22
G12 63.98 8.75 24 24 48 5.27 3.72 18 24 42 46.51 2.31 10 22 32 0.66 0.63 21 24 45 19.04 0.29 6 2 8
G13 43.28 8.01 21 8 29 9.55 3.78 20 8 28 60.23 3.62 17 8 25 1.01 0.44 14 8 22 17.32 0.15 1 8 9
G14 56.60 0.72 1 17 18 6.40 0.50 3 16 19 45.40 3.16 14 24 38 0.89 0.58 19 13 33 16.93 0.20 2 14 16
G15 66.49 5.74 16 11 27 8.59 3.52 17 10 27 55.90 0.80 3 14 17 0.95 0.42 13 12 25 17.29 0.22 5 10 15
G16 55.15 3.28 11 7 18 10.38 0.33 2 4 6 67.25 1.47 11 4 15 0.97 0.60 20 9 29 18.00 0.88 19 5 24
G17 67.08 1.38 4 12 16 7.44 0.88 8 14 22 55.69 0.78 2 15 17 0.95 0.14 1 11 12 15.63 0.21 3 20 23
G18 42.09 7.93 20 6 26 10.20 3.09 15 5 20 65.16 4.31 20 6 26 1.02 0.46 17 6 23 17.78 0.67 14 6 20
G19 42.03 2.87 9 19 28 6.09 1.61 13 20 33 56.12 0.77 1 13 14 0.71 0.28 8 21 29 16.66 0.60 12 16 28
G20 78.93 4.96 15 1 16 9.62 1.54 12 7 19 63.13 2.41 11 7 18 1.22 0.30 10 2 12 14.36 0.84 18 24 42
G21 70.87 2.66 8 4 12 12.06 2.64 14 1 15 68.44 0.87 4 3 7 1.01 0.16 3 7 9 19.74 0.80 16 1 17
G22 51.23 1.97 5 15 20 7.47 0.66 5 13 18 51.53 3.90 19 19 38 0.97 0.67 23 10 33 16.82 0.53 9 15 24
G23 54.61 0.82 2 13 15 6.85 0.78 7 15 22 48.45 2.88 12 21 33 1.08 0.30 9 5 14 14.56 0.67 13 23 36
G24 76.22 3.44 12 2 14 11.42 1.26 10 2 12 60.21 1.46 6 9 15 1.23 0.23 5 1 6 17.60 0.43 8 7 15
Sustainability 2023, 15, 1119 10 of 19
The mean vs stability biplots envisage the mean performance of the genotypes
through the environments. The line in Figures 5 and 6 passing through the origin repre-
sents the “average-environment coordinates”, and the right-hand side of the vertical line
symbolizes a higher mean yield for the genotypes. The second axis denotes stability. For
the cane yield, G21, G24, G16, G6, and G20 are positioned closer to the AEC, and the right-
hand side indicates that these are highly productive and stable genotypes for the cane
yield. Though genotypes G4, G18, G13 etc., are positioned towards a higher mean yield,
they are also unstable due to their far away position from the AEC line. For the CCS yield,
G20, G24, G21, G5, and G16 are located near the AEC towards the arrow, away from the
origin, which indicates their higher productiveness and stable performance for the trait.
The ranking of genotypes (Figures 7 and 8) revealed the best productiveness of gen-
otypes G21 and G24 for the cane yield, whereas G20, G24, G6, and G21 for the CCS yield
due to occupying the first concentric circles for these traits.
The GGE biplot polygons for the cane yield and CCS yield are displayed in Figures
9 and 10. Genotypes G4, G21, G18, G1, G2, G10, G12, and G5 were the vertex genotypes
for cane yield, whereas G13, G4, G20, G18, G2, G12, and G5 were the vertex genotypes for
the CCS yield, confirming the biggest distance from the origin. For the cane yield, the eight
environments were grouped into two mega-environments, i.e., the mega environment (i)
formed by E2 and the mega environment (ii) formed by E1, E3, E4, E5, E6, E7, and E8.
Genotypes G4, G21, and G18 were the vertexes of the mega environment (2) indicating
that they are better performers at all the studied levels of irrigation water salinity. For CCS
Sustainability 2023, 15, 1119 13 of 19
t ha−1 as well, the eight environments formed two mega groups (Figure 10) viz., the mega
environment (i) represented by E1, E2, E3, E4, E5, and E6 environments, whereas E7 and
E8 positioned in Mega environment (ii). G4 and G20 were the vertices genotypes in the
mega environment (i) whereas G18 was the vertices genotype in the mega environment
(ii), indicating their superior performance in these mega environments. There were also
vertexes of genotypes which were located in the regions with no environment at all, viz.,
G5, G12, G10, G2 for cane yield while G5, G12, G2, for CCS t ha−1, indicates their poor
performance in all the environments.
Figure 10. ‘Which won where’ polygon for CCS yield (t ha−1)..
Sustainability 2023, 15, 1119 14 of 19
4. Discussions
Identifying the salt-tolerant genotype with stable performance across different salin-
ity levels is a challenging task for any breeder due to very high environmental and GE
interactions. AMMI incorporates ANOVA and PCA into a single model and enables a
simple visual interpretation of the GE interaction. It enables the clustering of genotypes
based on the similarity of response characteristics and identifying potential trends across
environments [63]. In our study, a large sum of the square for environments indicated that
the environments were diverse, with large differences among environmental means, caus-
ing most of the variation in the cane yield, CCS yield, and NMC. The significant G × E
interaction indicated the differential response of the genotypes at different salinity levels.
A lot of findings are in support of the result that the environment’s main effect used to be
higher for the yield and related traits [64-66]. In our study, the AMMI model with only
two PCA interactions was the best predictive model, which is in agreement with many
researchers [65-70].
4.1. Biplot Analysis for Determination of Main Effect and Environment Influence
For the AMMI1 biplot, exposing main effects means on the abscissa and PC1 values
as the ordinates, genotypes, or environments that locate almost on a vertical line have
interrelated means and those that locate nearly on a horizontal line have similar interac-
tion patterns [64]. These authors proved that the genotypes/environments with great PC1
scores (positive or negative) have higher interactions, whereas genotypes/environments
with PC1 scores near zero have slight interactions [64]. In general, environments with
scores near zero have little interaction across environments and provide low discrimina-
tion among genotypes [68]. In our study, PC1 Vs CY (Cane yield), environments E5, E6,
E7, and E8 [higher ECiw 8 (E5, E6) and ECiw 12 (E7, E8)] demonstrated lower average main
effects and, thus, were rated as deprived environments. Environments E1 and E2 (Normal
ECiw) expressed the highest main effects and were gainful for most of the genotypes. The
PC1 scores for environments E3 and E4 (4 ECiw) are near zero, which indicates that ECiw 4
ds m−1 shows the least interaction among the studied environments in the expression of
the cane yield. Genotypes G20, G24, G21, G6, G4, G13, G8, and G15, expressed higher
main effects for the cane yield, which indicates their better adaptation under favorable
environments. Contrary, genotypes G12, G2, G10, G19, G1, and G18 exhibited lower main
effects for cane yield, indicating their specific adaptation under environments of higher
salinity [ECiw 8 (E5, E6) and ECiw 12 (E7, E8)]. The genotypes near the origin are indifferent
to the environmental interaction and vice versa [69]. The ideal environment and genotype
are those which are near the origin [34]. In our study, the cane yield genotypes G23, G24,
G6, G14, G3, G21, and G20, due to their position near the origin, are comparatively stable
under the various salinity environments (Figure 2a).
our earlier study, these entries were identified as tolerant or moderately tolerant against
salinity [5].
The sustainability index (SI) is the ratio of the average performance of the genotype
across the environments (excluding its standard deviation) to its best performance in a
particular environment [53]. It categorizes the genotypes into five groups viz., very low
(up to 20%), low (21–40%), moderate (41–60%), high (61–80%), and very high (above 80%).
This index is being used by various researchers in the selection of stable genotypes [70-
73]. In our study, except for a few (G18, G1, G10, G2, G16, G20 and G21 had moderate SI
for CY; G18 had moderate SI for CCS yield), most of the genotypes represent lower groups
of SI for the cane yield and CCS yield. This indicates that these traits were greatly affected
by the increased level of irrigation-induced salinity. On the contrary, NMC and SCW rep-
resent a moderate-to-high category of SI, which indicates a moderate reduction in the ex-
pression of these traits, with an increased level of irrigation-induced salinity stress and
the least impact on the juice quality as compared with yield and contributing traits.
whereas G20, G24, G6, and G21 were shown for the CCS yield due to occupying the first
concentric circles for these traits are the best productive genotypes.
The GGE biplot polygon recognized the pictorial grouping of environments based on
crossed GEI between the highest yield genotypes [81]. It is constructed by an asymmetrical
polygon. The number of lines starting at the bi-plot’s origin and intercepting the polygon
vertically is equal to the sides in the polygon. The genotypes that are out of the origin in
all directions polygons denote the vertices; hence all genotypes are inside the polygon
[78]. An imaginary environment is denoted by a line that vertically crosses a side of the
polygon, if both genotypes that formed that side, have better productivity, the genotype’s
comparative rank would be reversed in environments at the line’s opposite extreme
(crossed GE). Therefore, the lines radiating from the origin split the bi-plot into sections,
and each section had a vertex (genotype) that represents the best yield performance in
environments contained in that section, which is named a mega-environment. The vertex
genotypes are either the best or the poorest performers in some or all environments [60].
Genotypes G4, G21 and G18 were the vertexes of better performing mega environment
for cane yield, indicating that they are a better performer at all the studied levels of irri-
gation water salinity. For CCS t ha−1, the eight environments formed two mega groups
viz., mega environment (i) represented by E1, E2, E3, E4, E5, and E6 environments,
whereas E7 and E8 positioned in the mega environment (ii). G4 and G20 were the vertices
genotypes in the mega environment (i) whereas G18 was the vertices genotype in mega
environment (ii), indicating their superior performance in these mega environments.
There were also vertexes of genotypes which were located in the regions with no environ-
ment at all, viz., G5, G12, G10, G2 for cane yield while G5, G12, G2, for CCS t ha−1, indicates
their poor performance in all environments.
5. Conclusions
The genotype and environment main effects as well as G × E interaction effects were
significant for all the studied traits. The genotype G21 (Co 15023) was found as the most
stable genotype under different saline water environments, as it was among the best-
ranked genotypes for AMMI analysis, GSI, SI, and GGE biplot analysis for the CY and
CCS yield. The AMMI and GGE biplot analysis reveals the superiority of G6 (Co 0238) for
CY and CCS yield. Hence, the cultivation of these genotypes would help farmers to obtain
sustainable income in harsh environmental conditions.
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