Phenotypic correlations
The correlation coefficients among the studied traits ranged from
-0.86 to 0.99, indicating a wide spectrum of relationships between the parameters. Most of the correlations were positive, suggesting that an increase in one trait was generally associated with a proportional increase in others. However, negative correlations were observed between EP40 and body weights at different ages, ASM, BWFEP, WFE and EW40. The negative correlation with ASM implies that birds reaching sexual maturity earlier tend to demonstrate higher EP40, highlighting the advantage of early onset of lay in maximizing cumulative egg production. However, this early maturity may be associated with lower body weight. The inverse association with BWFEP and WFE suggests that birds with higher production levels may produce their first eggs at a lower body weight and with smaller initial egg size.
Phenotypic correlations revealed that ASM was negatively associated with egg production at 40 and 52 weeks (EP40:
r = -0.50; EP52:
r = -0.51), yolk height (YH:
r = -0.07), yolk diameter (YD:
r = -0.07) and yolk index (YI:
r = 0.02). The moderate negative correlations between ASM and egg production traits (EP40 and EP52) indicate that early-maturing individuals enter the laying phase sooner, thereby extending their productive period within a fixed timeframe. Conversely, delayed sexual maturity reduces the effective laying duration, resulting in lower overall egg output. In contrast, the correlations between ASM and yolk-related traits (YH, YD and YI) are negative but relatively weak in magnitude, suggesting only a minor influence of sexual maturity timing on internal egg quality characteristics. From a physiological perspective, these findings suggest that the mechanisms governing the onset of sexual maturity are more closely linked to reproductive efficiency (
i.e., egg number) than to egg quality parameters such as yolk morphology. Among all the examined relationships, WFE showed highly significant (
P<0.01) correlations with body weights at 8, 9, 12, 18, 21, 40 and 52 weeks of age, suggesting that early body growth is strongly related to the physiological onset of egg production. Moreover, the correlation between BW20 and BWFEP was also highly significant, underscoring the importance of pre-laying body weight in determining reproductive performance. In the present study, the correlation patterns among growth and reproductive traits were consistent with several previous reports.
In addition, YD and YH exhibited significant associations with both EW40 and EP40, further highlighting the interdependence between egg quality and production traits. Overall, the observed correlation pattern emphasizes the intricate relationship between growth performance, onset of sexual maturity and egg production parameters, providing valuable insights for genetic selection and management strategies aimed at improving both growth and reproductive efficiency. Similar findings of correlation coefficients were reported, in which body weight at 8 weeks was positively correlated with 12 week whereas its correlation with first egg weight and age at sexual maturity was relatively low. A negative phenotypic correlation of body weight at 10 to 20 weeks was found with age at sexual maturity. Moreover, body weight at 10 and 14 weeks was highly significant (p<0.001) with egg production at 52 weeks and egg weight at 40 weeks, respectively (
Yousefi Zonuz et al., 2013). In contrast, the opposite trend was observed in which ASM exhibited a positive correlation with egg production at both 40 and 52 weeks. Egg production at 40 weeks (EP40) showed a positive phenotypic association with egg production at 52 weeks (EP52) and egg weight at 52 weeks (EW52), but a negative correlation with egg weight at 40 weeks (EW40) and first egg weight (FEW). The relationship between EP40 and EW40 was statistically significant (
p<0.05), suggesting that birds that start laying earlier may initially produce smaller eggs but maintain better persistency of lay throughout the production cycle
(Liu et al., 2019). Consistent with these observations, body weight at 8 weeks was positively correlated with body weight at 12 and 16 weeks, although the correlation with egg production traits was relatively weak
(Dana et al., 2011). Collectively, these findings indicate that early growth traits are reliable indicators of later performance and can be used as indirect selection criteria for improving productivity. However, the moderate to low correlations observed between growth and reproductive traits also suggest that selection programs should balance both aspects to avoid antagonistic effects on age at sexual maturity and egg quality.
Principal component analysis
PCA was performed on twenty-three economic traits across three distinct genetic groups, namely Desi Cross 1, Desi Cross 2 and RIR. The results of the PCA provided valuable insights into the inter-relationships among growth, reproductive and egg quality traits in layer chickens. The Kaiser-Meyer-Olkin (KMO) measure of sampling adequacy is commonly used to assess whether the dataset is suitable for principal component analysis (PCA) by determining if each variable contains sufficient information for reliable factor extraction. A KMO value greater than 0.6 is generally considered acceptable, whereas values above 0.8 are regarded as highly desirable (
Tabachnick and Fidell, 2013). The sampling adequacy, as assessed by the Kaiser-Meyer-Olkin (KMO) statistic, was 0.931 (Table 1), indicating that the dataset was highly suitable for PCA. The overall significance of the correlation matrix was verified using Bartlett’s test of sphericity, which yielded a highly significant chi-square value (χ
2 = 59,285.377;
P<0.01) as illustrated in Table 1. Eigen values (Fig 1) and the percentage of variance explained by each component are presented in Table 2. Based on Kaiser’s criterion (Eigen value > 1), three principal components were retained, collectively accounting for 68.59% of the total variance. The component plot of the major components in rotated space is illustrated in Fig 2. The interpretation of the extracted components was carried out based on the factor loadings of individual traits on each principal component. Traits exhibiting high positive loadings within a component were considered to have strong associations, thereby representing a common underlying factor influencing performance. The first principal component (PC1) accounted for 54.366% of the total variance. This component was predominantly associated with body weight traits measured at various ages BW4, BW15, BW18, BW20, BW21, BW40, BW52, suggesting that this component captured growth-related attributes and highlighting its importance for economic efficiency. Moreover, since body weight is closely linked to feed efficiency, market value and overall production output, the dominance of this principal component underscores its relevance for economic efficiency. Selecting individuals with higher scores on this component could therefore lead to improved performance, reduced production costs and increased profitability in livestock systems. Among these, BW15 and BW18 exhibited particularly high component loadings, indicating that PC1 primarily represented overall body growth performance. The dominance of PC1, represented by body weight traits across different ages, underscores the significance of growth performance as a major determinant of overall productivity. The second principal component (PC2) explained 7.699% of the total variation and showed strong loadings on YD and YI, thus representing egg quality characteristics.
The coefficients of the rotated component matrix derived from PCA are presented in Table 3. The third principal component (PC3) contributed 6.525% of the total variance, with high loadings on YH. PC2 and PC3, which were defined by egg quality traits such as yolk diameter, yolk index and yolk height, reflect the influence of egg characteristics on market preference and breeding value. Communalities in PCA represent the proportion of each original variable’s variance explained by the retained PCs and range from 0 to 1. A high communality closer to 1, indicates the component model well explains that variable, while low values suggest the variable is not well explained.
Traits exhibiting higher communalities
, indicate their strong contribution to the explanation of total variance and their greater effectiveness in describing the economic traits of layer chickens. The communalities of the traits ranged from 0.096 (WFE) to 0.976 (BW18) (Table 3). Collectively, these components provide an integrated understanding of the underlying structure of performance variation among the genetic groups studied. In the present study, varimax rotation was applied to maximize the sum of squared loadings and facilitate the interpretability of extracted components (
Fernandez, 2010). Comparable studies have demonstrated similar trends in which the total variation of body weight was determined, with the first three PCs explaining 67.78% and 65.93% of the total variance of the morphostructure of male and female birds, respectively. The KMO value of 0.80, indicates the robustness of the PCA results, which concluded, that the body measurements of PC1 were influenced by the BW of birds (
Tamzil and Putra, 2024). A similar trend was depicted in which PC1 had the largest share of body weight.
The second component explained 27.072% of total variation, consistent with the pattern of major components contributing significantly to morphometric variation
(Vilakazi et al., 2020). A study was conducted where the first component illustrated body size and explained about 36% of total variation
(Mishra et al., 2017). Likewise, PC1, explaining 38.3% of total variation, was documented, further confirming the prominence of body weight traits in defining structural variation
(Egena et al., 2014). A similar trend was identified with four principal components explaining a total of 69.52% of variation, with the first component alone accounting for 28.68%, emphasizing the consistent contribution of PC1 across diverse chicken populations
(Dahiya et al., 2020). Similar studies conducted on internal egg quality and performance traits of native hens revealed that the application of PCA could effectively reduce the computing cost and time required for genetic evaluation of multiple traits
(Babajani et al., 2018).
A comparable study was also reported in which PC1 loaded mostly on the size and weight of albumen and yolk for 22 egg quality traits of chickens, whereas the five principal components extracted accounted for 79.70% of the total variance
(Goto et al., 2015). The comparatively higher proportion of variance explained may be attributed to differences in the genetic background of the chicken population, degree of trait intercorrelation, environmental uniformity and the nature of the traits included in the analysis. Moreover, egg quality traits are often more closely associated physiologically than combined growth and performance traits, resulting in greater clustering of variability within fewer components.