Skip to main content
Scientifica logoLink to Scientifica
. 2017 Dec 3;2017:5202913. doi: 10.1155/2017/5202913

Genetic Variability of Exotic Sugarcane Genotypes

M N Alam 1,, Ujjal Kumar Nath 2, K M R Karim 3, M M Ahmed 1, R Y Mitul 2
PMCID: PMC5733769  PMID: 29348970

Abstract

Sugarcane is the main sugar producing crop in Bangladesh. However, improvement of this crop through breeding is limited due to lack of genetic diversity. Therefore, genetic variability and diversity assessment are necessarily important for the foreign introduced materials. Experiment was conducted with 9 exotic sugarcane genotypes at Regional Station, Bangladesh Sugar Crop Research Institute, Gazipur, during 2012-13, following RCBD. Data were collected on different growth and yield contributing characters. Individual cane weight exhibited high genotypic coefficient of variation and phenotypic coefficient of variation. Leaf blade length, leaf blade width, fresh leaf weight, dried leaf weight, number of tillers, millable cane, bud size, cane diameter, internodes number, internode length, plant height, stalk length, brix%, and individual cane weight showed high heritability. Individual cane weight showed highly significant and positive correlation with cane diameter, internode length, and stalk length, whereas path coefficient analysis revealed that cane diameter had maximum positive direct effect on individual cane weight followed by internode length, number of tillers, and chlorophyll content. Results indicate that the genotypes should be selected on the basis of individual cane weight, cane diameter, and millable canes number for future breeding to get higher sugarcane yield in respect to juice and brix content.

1. Introduction

Sugarcane is the leading sugar producing crop in the world as well as in Bangladesh. It provides about 75% of the sugar harvested for human consumption [1, 2]. The average yield of sugarcane in Bangladesh is about 41.2 tons/hectare which is far below from the existing standard; therefore, possibilities could be exploited through collaboration among research stations and progressive growers [3]. Sugarcane is a long duration field crop which occupies the land up to 12–18 months for its maturity. It is considered as a time-consuming crop compared to other traditional field crops grown in Bangladesh. Therefore, sustainability of sugarcane cultivation in this country is threatened. To sustain sugarcane production and to improve the productivity, tolerance to biotic and abiotic stresses, nutrient management, and improved sugar recovery are of the major concerns. Development of varieties is important consideration that would be highly productive and tolerant against biotic and abiotic factors with the changing climate. Coefficients of variation with heritability as well as genetic advance are very essential to improve any trait of sugarcane because this would help in informing whether or not the desired objective can be achieved from the material [4]. Therefore, the objective of present study was to narrate the nature and extent of genetic variability and phenotypic and genotypic variability of sugarcane varieties in some exotic traits in Bangladesh.

2. Materials and Methods

The experiment was conducted at Regional Station, Bangladesh Sugar crop Research Institute, Gazipur, during 2012-13 cropping season under Madhupur Tract soil, following Randomized Completely Block Design (RCBD) with three replicates. Nine exotic genotypes of sugarcane, namely, GT11, GT15, GT17, VMC86-550, HoCP85-845, HoCP96-540, HoCP95-988, HoCP91-555, and CB45-3, were collected from Quarantine Station, Bangladesh Sugar Crop Research Institute, Gazipur. The two-eyed setts of each genotype were planted in 6 m × 5 m size plot. Line to line distance was 1 m and plot to plot was 2 m. Setts were placed in the furrow following end to end method. Data were collected on different growth and yield contributing characters. Intercultural operations like weeding, earthen-up, mulching, and irrigation were done as per required schedule. Leaf chlorophyll content (SPAD index) was estimated using a SPAD-502 plus chlorophyll meter [5]. The collected data were analyzed by different statistical software, namely. MSTAT-C [6], PLABSTAT, and STAR [7] program for variability and diversity analysis. Analysis of variance was performed using the Plant Breeding Statistical Program [8].

2.1. Estimation of Genotypic and Phenotypic Variances

Genotypic and phenotypic variances were calculated using the following formula [9, 10]:

Genotypicvarianceσg2=GMSEMSr, (1)

where GMS is genotypic mean square, EMS is error mean square, r is number of replication, and phenotypic variance is (σp2) = σg2 + σe2.

2.2. Estimation of Genotypic Coefficient of Variation (GCV) and Phenotypic Coefficient of Variation (PCV)

Phenotypic (PCV) and genotypic (GCV) coefficients of variation were evaluated according to the methods as follows [1013]:

GenotypiccoefficientofvariationGCV=σg2X×100, (2)

where σg2 is genotypic variance and X- is population mean.

PhenotypiccoefficientofvariationPCV=σp2X×100, (3)

where σp2 is phenotypic variance and X- is population mean.

2.3. Estimation of Heritability

Broad-sense heritability (h2) for mean values was calculated using PABSTAT [8], following the formula described by [9, 10, 14, 15]:

Heritabilityhb2=σg2σp2×100, (4)

where σg2 is genotypic variance and σp2 is phenotypic variance.

2.4. Estimation of Genetic Advance

Genetic advance (GA) was estimated accordance to the methods illustrated [10, 16, 17]:

GeneticadvanceGA=hb2·K·σp, (5)

where hb2 is heritability in broad sense, K = K is the selection differential value which is 2.06 at 5% selection intensity, and σp is phenotypic standard deviation.

2.5. Estimation of Correlation Coefficient

The genotypic and phenotypic correlation coefficients between growth and yield contributing character were calculated as follows [13]:

Genotypiccorrelation,rgxy=Covg1.2σ2g1σ2g2. (6)

Cov(g)1.2 is genotypic covariance between the variables X and Y, σ2(g)1 is genotypic variance of the variable X1, and σ2(g)2 is genotypic variance of the variable X2.

Phenotypiccorrelation,rpxy=Covp1.2σ2p1σ2p2. (7)

Cov(p)1.2 is phenotypic covariance between the variables X and Y, σ2(p)1 is phenotypic variance of the variable X1, and σ2(p)2 is Phenotypic variance of the variable X2.

2.6. Estimation of Path Coefficient

Direct and indirect path coefficient was calculated as described [18]:

ryi=Pyi+i=1i=1kriiPyifori1, (8)

where ryi is the correlation coefficient between the ith causal variable (Xi) and effect variable (y), rii is the correlation coefficient between the ith and i′th causal variables, Pyi is the path coefficient (direct effect) of the ith causal variable (Xi), and riiPyi is the indirect effect of the ith causal variable via the i′th causal variable. To determine the direct effect, square matrices of the correlation coefficients between independent traits in all possible pairs were inverted and multiplied by the correlation coefficient between the independent and dependent traits.

3. Results and Discussion

3.1. Variance Components

The analysis of variance for all characters showed statistically highly significant (p ≤ 0.01) among the genotypes except chlorophyll (Table 1). Similar results were also found in case of number of millable canes, individual cane weight, cane height, and sucrose% [19]. These results indicated that there were greater variations among the exotic genotypes that might support the design of a breeding program for sugarcane improvement. As stated, the PCV (phenotypic coefficient of variation) and GCV (genotypic coefficient of variation) values are ranked as low, medium, and high with 0 to 10%, 10 to 20%, and >20%, respectively [20]. High GCV were recorded for fresh leaf weight (22.51), millable cane (22.28), bud size (24.02), and individual cane weight (37.79); while leaf blade width (19.43), dried leaf weight (15.42), number of tillers (16.20), and cane diameter (17.58) showed medium GCV and leaf blade length (4.45), chlorophyll content (5.39), number of internodes (5.00), internode length (8.55), plant height (7.14), stalk length (4.38), and brix% (7.05) exhibited low GCV. High phenotypic coefficients of variation (PCV) were also recorded for leaf blade width (20.31), fresh leaf weight (22.78), millable cane (23.19), bud size (24.87), and individual cane weight (37.96) but moderate PCVs were recorded for dried leaf weight (18.26), number of tillers (17.64), cane diameter (18.16), and chlorophyll content (11.88); in contrast, remaining traits showed low PCV (Table 2). High genotypic coefficient of variation (37.79) and phenotypic coefficient of variation (37.96) were found in individual cane weight [21]. The estimated phenotypic coefficient of variation (PCV) was higher than genotypic coefficient of variation (GCV) for all the traits indicating greater environmental influence on these traits for total variation. High GCV and PCV indicated that selection may be effective based on these characters and their phenotypic expression would be good indication of the genotypic potential [22]. Mean performance of different genotypes had wider variation in performance values for different traits (Table 3).

Table 1.

Analysis of variances for 15 characters of 9 exotic sugarcane genotypes.

Sources df LBL LBW FLW DLW NT MC Bud size Chlorophyll content Cane diameter Number of internodes Internode length Plant height Stalk length Brix% ICW
Genotype 8 125.15 1.45 1906.43 84.37 12.34 14.91 252.24 46.67 0.42 8.04 2.71 0.32 0.19 6.00 0.72
Replication 2 2.81 0.01 5.15 29.48 1.59 2.01 13.70 0.62 0.01 1.93 0.81 0.12 0.02 2.02 0.00
Error 16 4.95 0.04 15.19 9.98 0.72 0.41 5.94 26.25 0.01 1.30 0.06 0.02 0.01 0.37 0.00

Note. LBL = leaf blade length, LBW = leaf blade width, FLW = fresh leaf weight, DLW = dried leaf weight, NT = number of tillers, MC = millable cane, BS = bud size, chlorophyll, CD = cane diameter, NI = number of internodes, IL = internode length, PH = plant height, SL = stalk length, brix%, and ICW = individual cane weight.

Table 2.

Component for variances, heritability in broad sense (hb2), and genetic advance (GA) for 15 variables of 9 exotic sugarcane genotypes.

Characters GV EV PV GCV PCV Heritability (hb2) GA
Leaf blade length 40.07 4.947 45.02 4.45 4.71 94.3 61.456
Leaf blade width 0.47 0.043 0.51 19.43 20.31 95.7 28.618
Fresh leaf weight 630.41 15.190 645.60 22.51 22.78 98.8 1178.444
Dried leaf weight 24.80 9.982 34.78 15.42 18.26 84.4 187.288
Number of tillers 3.88 0.718 4.59 16.20 17.64 91.9 71.525
Millable cane 4.84 0.405 5.24 22.28 23.19 96.1 105.069
Bud size 82.10 5.935 88.04 24.02 24.87 96.6 464.190
Chlorophyll 6.80 26.253 33.06 5.39 11.88 45.4 63.850
Cane diameter 0.14 0.009 0.15 17.58 18.16 96.8 13.873
Number of internodes 2.25 1.301 3.55 5.00 6.29 79.6 19.402
Internode length 0.88 0.061 0.94 8.55 8.84 96.7 17.106
Plant height 0.10 0.017 0.12 7.14 7.69 92.8 5.075
Stalk length 0.02 0.011 0.03 4.38 5.63 77.9 1.489
Brix% 1.88 0.370 2.25 7.05 7.71 91.4 21.757
Individual cane weight 0.24 0.002 0.24 37.79 37.96 99.6 38.115

Note. GV = genotypic variance, EV = error variance, PV = phenotypic variance, GCV = genotypic coefficient of variation, and PCV = phenotypic coefficient of variation.

Table 3.

Mean performance of the exotic nine genotypes for 15 different variables.

Variables Genotypes
GT 11 GT 15 GT 17 VMC
86-550
HoCP
85-845
HoCP
96-540
HoCP
95-988
HoCP
91-555
CB 45-3 ±LSD(0.05)
Leaf blade length (cm) 143.28 143.71 150.35 143.66 133.28 132.03 140.53 150.82 143.60 3.85
Leaf blade width (cm) 4.56 4.31 3.87 3.62 3.69 3.16 3.0 3.12 2.33 0.36
Fresh leaf weight (g) 136.67 133.33 128.67 144.33 106.00 89.33 85.33 105.33 74.67 6.75
Dried leaf weight (g) 38.67 38.00 37.33 36.00 31.33 25.33 28.0 30.00 26.00 5.47
Number of tillers/m2 9.67 10.33 13.00 11.67 12.00 10.33 13.33 12.67 16.33 1.47
Millable cane/m2 8.00 7.33 10.33 9.67 9.67 7.67 11.0 10.50 14.67 1.10
Bud size (mm2) 40.50 53.84 29.82 46.58 39.33 36.20 32.05 22.68 38.58 4.22
Chlorophyll (spad) 48.67 45.03 46.07 49.23 49.53 57.40 43.97 49.23 46.33 8.87
Cane diameter (cm) 2.64 2.35 2.45 2.29 1.89 1.96 2.0 2.07 1.36 0.17
Number of internodes 30.00 33.00 29.00 28.67 29.33 30.00 29.0 32.33 28.33 1.97
Internode length (cm) 12.24 12.19 11.47 11.06 9.44 11.34 10.64 10.57 9.92 0.43
Plant height (m) 4.82 4.76 4.93 3.90 4.40 4.61 4.45 4.41 4.16 0.22
Stalk length (m) 3.13 3.05 3.14 3.15 2.38 3.01 2.76 2.99 2.77 0.18
Brix% 19.83 19.38 19.02 19.77 20.22 20.54 20.41 19.83 15.88 1.05
Individual cane weight (kg) 1.88 1.68 1.64 1.48 0.78 1.2 1.0 1.57 0.39 0.08

3.2. Heritability and Genetic Advance

Heritability values are categorized as low (0–30%), moderate (30–60%), and high (60% and above) [23]. The characters of leaf blade length, leaf blade width, fresh leaf weight, dried leaf weight, number of tillers, millable cane, bud size, cane diameter, number of internodes, internode length, plant height, stalk length, brix%, and individual cane weight showed high heritability except chlorophyll content (45.3%) (Table 2). The heritability for millable canes number (88%), stalk diameter (85%), and cane weight (84%) were also reported in sugarcane [19]. Similar results were found for those characters [16, 22]. It indicates that simple selection based on phenotype for these traits might be effective method for sugarcane variety improvement breeding program. The highest genetic advance was found in millable cane (10.645) and the lowest in stalk length (0.005; Table 2).

3.3. Correlation Coefficient

The pairwise simple correlation coefficient (r) among various variables of nine exotic genotypes is presented in Table 4. Individual cane weight showed positive and highly significant correlation with cane diameter (r = 0.942∗∗), internode length (r = 0.837∗∗), and stalk length (r = 0.775). There was also positive significant correlation of individual cane weight with leaf blade width (r = 0.784), fresh leaf weight (r = 0.807∗∗), dried leaf weight (r = 0.765), nonsignificant positive correlation with leaf blade length (r = 0.453), bud size (r = 0.078), chlorophyll content (r = 0.014), number of internodes (r = 0.523), plant height (r = 0.522), and brix% (r = 0.482). By contrast, number of tillers (r = −0.721) and millable cane (r = −0.707) had negative significant correlations with individual cane weight. Positive and highly significant correlation between cane yield and its components, namely, single cane weight, stalk length, and millable canes number, was reported [2426]. It was also observed that cane diameter has significant positive correlation with cane yield [27]. Millable canes number had negatively significant correlation with cane diameter (r = −0.722), internode length (r = −0.676), and brix% (r = −0.742). It was also reported that millable canes number had negative significant correlation with cane diameter (r = −0.722) [24]. It is obvious that single cane weight, stalk length, millable canes number, stalk diameter, and number of internodes can be considered together in a positive direction towards an ultimate aim of developing high yielding sugarcane clone.

Table 4.

Correlation coefficient matrix among different characters in 9 exotic sugarcane genotypes.

Variables Leaf blade length Leaf blade width Fresh leaf weight Dried leaf weight Number of tillers Millable cane Bud size Chlorophyll content Cane diameter Number of internodes Internode length Plant height Stalk length Brix%
Leaf blade width 0.090
Fresh leaf weight 0.354 0.856∗∗
Dried leaf weight 0.438 0.892∗∗ 0.945∗∗
Number of tillers 0.276 −0.795 −0.613 −0.506
Millable cane 0.279 −0.777 −0.581 −0.484 0.981∗∗
Bud size −0.300 0.442 0.439 0.425 −0.373 −0.369
Chlorophyll content −0.552 −0.080 −0.123 −0.357 −0.421 −0.393 −0.099
Cane diameter 0.322 0.891∗∗ 0.865∗∗ 0.856∗∗ −0.741 −0.722 0.171 −0.077
Number of internodes 0.235 0.370 0.247 0.248 −0.471 −0.525 0.104 0.004 0.315
Internode length 0.264 0.693 0.627 0.639 −0.676 −0.674 0.345 0.001 0.795 0.420
Plant height 0.122 0.570 0.212 0.387 −0.433 −0.494 −0.108 −0.060 0.546 0.378 0.598
Stalk length 0.540 0.377 0.579 0.500 −0.378 −0.359 0.088 0.073 0.646 0.242 0.831∗∗ 0.267
Brix% −0.329 0.455 0.304 0.170 −0.742 −0.759 −0.081 0.352 0.543 0.278 0.251 0.239 0.054
Individual cane weight 0.453 0.784 0.807∗∗ 0.765 −0.721 −0.707 0.078 0.014 0.942∗∗ 0.523 0.837∗∗ 0.522 0.775 0.482

, ∗∗Significant at 5% and 1%, respectively.

3.4. Path Coefficient Analysis

Path coefficient analysis was performed to partition the correlation coefficient value towards individual cane weight into direct and indirect effect to get the real scenario of that trait into target variable. The results of path coefficient analysis revealed that cane diameter had maximum positive direct effect on individual cane weight (0.748) followed by internode length (0.676), number of tillers (0.410), chlorophyll (0.308), dried leaf weight (0.272), leaf blade length (0.229), and number of internodes (0.188) (Table 5). Path coefficient analyses indicated that plant height was less important contributors than stalk diameter and stalk number for enhancing cane yield [28]. It was reported that numbers of internodes were the major contributors to cane yield per plot [29]. This study indicates that cane diameter, number of internodes, length of internode, and stalk length were most important for getting higher individual cane weight as well as improvement of sugarcane yield. Therefore, selection based on number of millable canes and single cane weight might directly increase sugarcane yield.

Table 5.

Path coefficient analysis showing direct (diagonal) and indirect effects of different characters on individual cane weight of sugarcane genotypes.

Characters LBL LBW FLW DLW NT MC BS Chlorophyll CD NI IL PH SL Brix
LBW 0.229 −0.007 −0.037 0.119 0.113 −0.102 0.068 −0.170 0.241 0.044 0.179 −0.040 −0.203 0.017
FLW 0.021 −0.075 −0.090 0.243 −0.327 0.283 −0.101 −0.025 0.667 0.070 0.469 −0.186 −0.141 −0.024
DLW 0.081 −0.065 −0.104 0.257 −0.252 0.212 −0.100 −0.038 0.648 0.047 0.424 −0.069 −0.217 −0.016
NT 0.100 −0.067 −0.099 0.272 −0.208 0.176 −0.097 −0.110 0.641 0.047 0.432 −0.126 −0.188 −0.009
MC 0.063 0.060 0.064 −0.138 0.410 −0.357 0.085 −0.130 −0.555 −0.089 −0.457 0.141 0.142 0.039
BS 0.064 0.059 0.061 −0.132 0.403 −0.364 0.084 −0.121 −0.541 −0.099 −0.456 0.161 0.135 0.040
Chlorophyll −0.069 −0.033 −0.046 0.116 −0.153 0.134 −0.228 −0.030 0.128 0.020 0.233 0.035 −0.033 0.004
CD −0.126 0.006 0.013 −0.097 −0.173 0.143 0.023 0.308 −0.058 0.001 0.001 0.020 −0.027 −0.018
NI 0.074 −0.067 −0.090 0.233 −0.305 0.263 −0.039 −0.024 0.748 0.060 0.538 −0.178 −0.242 −0.028
IL 0.054 −0.028 −0.026 0.067 −0.194 0.191 −0.024 0.001 0.236 0.188 0.284 −0.123 −0.091 −0.014
PH 0.060 −0.052 −0.066 0.174 −0.278 0.246 −0.079 0.000 0.595 0.079 0.676 −0.195 −0.312 −0.013
SL 0.028 −0.043 −0.022 0.105 −0.178 0.180 0.025 −0.018 0.409 0.071 0.405 −0.326 −0.100 −0.012
Brix 0.123 −0.028 −0.061 0.136 −0.155 0.131 −0.020 0.022 0.484 0.046 0.562 −0.087 −0.375 −0.003
ICW −0.075 −0.034 −0.032 0.046 −0.305 0.277 0.018 0.108 0.407 0.053 0.170 −0.078 −0.020 −0.052
Residual effect = 0.019

Note. LBL = leaf blade length, LBW = leaf blade width, FLW = fresh leaf weight, DLW = dried leaf weight, NT = number of tillers, MC = millable cane, BS = bud size, chlorophyll, CD = cane diameter, NI = number of internodes, IL = internode length, PH = plant height, SL = stalk length, brix%, and ICW = individual cane weight.

3.5. Divergence of Genotypes

All the genotypes were clustered on the basis of agglomerative cluster analysis, where specifications were made based on Euclidean distance matrix (Table 6) and grouping was made on average clustering method. Based on these two methods together the nine genotypes were clustered into three groups named as cluster I, cluster II, and cluster III (Figure 1). Cluster II included 4 genotypes (GT 11, GT 15, GT 17, and VMC 86-550). Similarly, cluster III also included 4 genotypes (HoCP85-845, HoCP95-988, HoCP91-555, and HoCP96-540). By contrast, only genotype CB45-3 belonged to cluster I.

Table 6.

Euclidean distance matrix for 15 characters of 9 exotic sugarcane genotypes.

Genotypes GT 11 GT 15 GT 17 VMC 86-550 HoCP 85-845 HoCP 96-540 HoCP 95-988 HoCP 91-555 CB 45-3
GT 11 0 2.773618 3.147112 3.972764 6.141488 5.404492 5.806524 5.1793 9.16596
GT 15 2.773618 0 4.367265 4.508293 6.214665 5.954076 5.983032 5.355682 8.923348
GT 17 3.147112 4.367265 0 4.097314 5.794336 5.814613 4.434417 3.806455 7.27551
VMC 86-550 3.972764 4.508293 4.097314 0 4.92496 5.140553 4.613214 4.588661 7.020552
HoCP 85-845 6.141488 6.214665 5.794336 4.92496 0 4.417262 3.307413 5.016917 5.896278
HoCP 96-540 5.404492 5.954076 5.814613 5.140553 4.417262 0 4.538716 4.798698 7.331457
HoCP 95-988 5.806524 5.983032 4.434417 4.613214 3.307413 4.538716 0 3.588104 4.84463
HoCP 91-555 5.1793 5.355682 3.806455 4.588661 5.016917 4.798698 3.588104 0 6.315618
CB 45-3 9.16596 8.923348 7.27551 7.020552 5.896278 7.331457 4.84463 6.315618 0

Figure 1.

Figure 1

Dendrogram based on mean performance of variables among 9 exotic sugarcane genotypes according to average clustering and Euclidean distance method, where 1 is GT11, 2 is GT15, 3 is GT17, 4 is VMC86-550, 5 is HoCP85-845, 6 is HoCP96-540, 7 is HoCP95-988, 8 is HoCP91-555, and 9 is CB45-3.

4. Conclusion

The study indicated that there is wide genetic variability among the tested genotypes for growth and yield characters. Moreover, the results showed high GCV for millable cane (22.28) and individual cane weight (37.79), while leaf blade length (4.45), chlorophyll content (5.39), number of internodes (5.00), internode length (8.55), plant height (7.14), stalk length (4.38), and brix% (7.05) showed low GCV. High phenotypic coefficient of variation was also recorded for millable cane (23.19) and individual cane weight (37.96). Path coefficient value in plant height is less important than stalk diameter and stalk number as a component of cane yield. Therefore, path coefficient, GCV, and PCV together might be helpful for effective selection. However, selection of candidate genotypes should also be performed considering those characters with high values of heritability because they magnify the genetic advance to progenies.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of the paper.

References

  • 1. FAO (Food and Agricultural Organization): Economic and Social Department: The Statistical Division, 2009.
  • 2.Sreenivasan T., Ahloowalia B., Heinz D. Cytogenetics. Vol. 11. Amsterdam, Netherlands: Elsevier; 1987. Sugarcane improvement through breeding; pp. 211–253. (Developments in Crop Science). [DOI] [Google Scholar]
  • 3.TNAU (Tamil Nadu Agricultural University) Agritech portal: Expert System for Sugarcane. http://agritech.tnau.ac.in/, 2013.
  • 4.Tyagi S. D., Singh D. N. Studies on genetic variability for stalk characters in sugarcane. Indian Sugar XL VIII. 1998:259–262. [Google Scholar]
  • 5.Markwell J., Osterman J. C., Mitchell J. L. Calibration of the Minolta SPAD-502 leaf chlorophyll meter. Photosynthesis Research. 1995;46(3):467–472. doi: 10.1007/BF00032301. [DOI] [PubMed] [Google Scholar]
  • 6.Russell D. F. MSTAT-C Computer Package Programme. USA: Crop and Soil Science Department, Michigan State University; 1986. [Google Scholar]
  • 7. STAR: Statistical Tool for Agricultural Research, Biometrics and Breeding Informatics, Plant Breeding, Genetics and Biotechnology Division, International Rice Research Institute, 2014.
  • 8.Utz HF: PLABSTAT (Version 2N) A computer program for the computation of variances and covariance's. Institute of Plant Breeding, Seed Science, and Population Genetics, University of Hohenheim, Stuttgart, Germany. http://www.unihohenheim.de/ipspwww/soft.html, 2007.
  • 9.Hill J., Becker H. C., Tigerstedt P. M. Quantitative and Ecological Aspects of Plant Breeding. London, UK: Chapman & Hall; 1998. [Google Scholar]
  • 10.Johnson H. W., Robinson H. F., Comstok R. E. Estimation of genetic and environmental variability in soybean. Agronomy Journal. 1955;47:314–318. doi: 10.2134/agronj1955.00021962004700070009x. [DOI] [Google Scholar]
  • 11.Burton G. W. Quantitative inheritance in pearl millet (Pennisetum glaucum S. H.) Agronomy Journal. 1952;43:409–417. [Google Scholar]
  • 12.Kumar A., Misra S. C., Singh V. P., Chaahan B. P. S. Variability and correlation studies in triticale. Journal of the Maharashira Agricultural University. 1985;10:273–275. [Google Scholar]
  • 13.Singh R. K., Chaudhary B. D. Biometrical Methods in Quantitative Genetic Analysis. New Delhi, India: Kalyani Publishers; 1985. [DOI] [Google Scholar]
  • 14.Allard R. W. Principles of Plant Breeding. New York, NY, USA: John Wily and Sons. Inc; 1960. [Google Scholar]
  • 15.Hanson C. H., Robinson H. F., Comstock R. E. Biometrical studies of yield in segregating populations of korean lespedeza. Agronomy Journal. 1956;48(6):268–272. doi: 10.2134/agronj1956.00021962004800060008x. [DOI] [Google Scholar]
  • 16.Nair N. V., Balakrishnan R., Sreenivasan T. V. Variability for quantitative traits in exotic hybrid germplasm of sugarcane. Genetic Resources and Crop Evolution. 1998;45(5):459–464. doi: 10.1023/A:1008696617524. [DOI] [Google Scholar]
  • 17.Fehr W. R. Principles of Cultivar Development. I. New York, NY, USA: MacMillan; 1987. [Google Scholar]
  • 18.Lynch M., Walsh B. Genetics and Analysis of Quantitative Traits. Sunderland, Mass, USA: Sin. Associates Inc.; 1998. [Google Scholar]
  • 19.Chaudhary R. R. Genetic variability and heritability in sugarcane. Nepal Agriculture Research Journal. 2001;4(5):56–59. [Google Scholar]
  • 20.Shivasubramanian S., Menon M. Heterosis and inbreeding depression in rice. Madrash Agricultural Journal. 1973;60:1139. [Google Scholar]
  • 21.Singh R., Sangwan R. S. Studies on genetic variability for stalk characters in sugarcane. Indian Sugar. 1980;30:409–412. [Google Scholar]
  • 22.Singh R. K., Singh D. N., Singh S. K., Singh H. N. Genetic variability and correlation studies in foreign commercial hybrids of sugarcane. Agricultural Science Digest. 1994;14:103–107. [Google Scholar]
  • 23.Robinson H. F., Comstock R. E., Harvey P. H. Estimates of heritability and the degree of dominance in corn. Agronomy Journal. 1949;41(8):353–359. doi: 10.2134/agronj1949.00021962004100080005x. [DOI] [Google Scholar]
  • 24.Balasundarum N., Bhagyalkshmi KV. Variability, heritability and association among yield and yield components in sugarcane. Indian Journal of Agricultural Sciences. 1978;48:291–295. [Google Scholar]
  • 25.Brown A. H. D., Daniels J., Latter B. D. H. Quantitative genetics of sugarcane - II. Correlation analysis of continuous characters in relation to hybrid sugarcane breeding. Theoretical and Applied Genetics. 1969;39(1):1–10. doi: 10.1007/BF00283078. [DOI] [PubMed] [Google Scholar]
  • 26.Punia M. S., Paroda R., Hooda R. S. Correlation and path analysis of cane yield in sugarcane. Indian Journal of Genetics and Plant Breeding. 1983;43:109–112. [Google Scholar]
  • 27.Hooda R. S., Babu C. N., Khairwal L. S. Association and path analysis of nine characters in progenies of four sugarcane crosses at settling stage. Indian Journal of Agricultural Sciences. 1979;49:931–933. [Google Scholar]
  • 28.Kang M. S., Miller J. D., Tai P. Y. Genetic and Phenotypic Path Analyses and Heritability in Sugarcane1. Crop Science. 1983;23(4):p. 643. doi: 10.2135/cropsci1983.0011183X002300040010x. [DOI] [Google Scholar]
  • 29.Thippeswamy S., Kajjidoni S. T., Salimath P. M., Goud J. V. Correlation and path analysis TNAU (Tamil Nadu Agricultural University) Agritech portal: Expert System for Sugarcane. http://agritech.tnau.ac.in/, 2003.

Articles from Scientifica are provided here courtesy of Wiley

RESOURCES