Acta agriculturae Slovenica, 119/2, 1–13, Ljubljana 2023 doi:10.14720/aas.2023.119.2.2949 Original research article / izvirni znanstveni članek Variability of genetic - morphological traits of eleven seed strains of Mangifera indica L. growing in Upper Egypt Hoida ZAKI 1, 2 , Mona Mohamed MANSOUR 3 , Samah Osman Ahmed OSMAN 3 , Nagwa Rabie Ahmed HUSSEIN 1 Received December 04, 2022; accepted April 26, 2023. Delo je prispelo 4. decembra 2022, sprejeto 26. aprila 2023 1 Botany and Microbiology Department, Faculty of Science, Qena, South Valley University, Egypt 2 Corresponding author, e-mail: hoaida.zaki@sci.svu.edu.eg 3 Tropical Fruits Department, Horticulture Research Institution, Agricultural Research Centre, Egypt Variability of genetic - morphological traits of eleven seed strains of Mangifera indica L. growing in Upper Egypt Abstract: Mango (Mangifera indica L.) is one of the tasti- est fruits in the world, with numerous advantages beyond their economic value. Eleven genotypes of mango various cultivars were examined for variability, heritability, and genetic advance, as well as multivariate analysis based on cluster and principal component analysis (PCA) for yield and some of its contribut- ing traits during the two growing seasons, 2021 and 2022. All studied traits showed significant differences, and the pheno- typic coefficients of variation (PCV) were found to be higher than genotypic coefficients of variation (GCV), supporting the idea that morphological (genetic) traits are more prevalent than environmental influence. All traits had substantial heritability ranging from 75.63 to 99.93 %, and the highest significant ge- netic advance (119.09 %) was for the number of fruits per tree than other traits. Four clusters were formed, i.e., clusters I and IV had four genotypes, cluster II had two, and cluster III had one genotype. The highest cluster mean values for fruit diam- eter, fruit mass, yield per tree, and the number of fruits per tree were found in Cluster II, followed by cluster I. Greater genetic divergence was found between ‘Zebda’ or ‘S9’ or ‘S10’ with most other genotypes, indicating that these genotypes may be used to study the characters’ broad range of variability and to yield high-quality recombinant lines. In light of the fact that mango is a very heterozygous crop, our current genetic results can be used for the selection of the appropriate parents in hy- bridization programs and in vegetative propagation to yield selective traits. Key words: Mangifera indica; mango genotypes; genetic variation; principal component analysis; heritability Spremenljivost genetskih (morfoloških) lastnosti sedmih se- menskih linij manga (Mangifera indica L.) rastočega v Zgor- njem Egiptu Izvleček: Mango (Mangifera indica L.) je eden izmed najokusnejših sadežev na svetu s številnimi prednostmi poleg njihove cene. Preučevanih je bilo enajst genotipov manga raz- ličnih sort glede na njihovo variabilnost, dednost in genetsko prednost. Opravljena je bila multivariatna analiza, ki je temelji- la na analizi grozdov in glavnih component (PCA) za pridelek in nekaterih z njim povezanih lastnosti v dveh rastnih sezonah, 2021 in 2022. Vse preučevane lastnosti so pokazale značilne razlike, kjer je imel fenotipski koeficient spremenljivosti (PCV) večje vrednosti kot genotipski koeficient raznolikosti (GCV), kar podpira idejo, da so morfološke (genetske) lastnosti pre- vladujoče nad okoljskimi vplivi. Vse lastnosti so imele znatno dednost, ki je znašala od 75,63 do 99,93 %. Največja značilna genetska prednost (119,09 %) je bila ugotovljena za za število plodov na drevo. Izoblikovale so se štiri skupine in sicer skupini I in IV s štirimi genotipi, skupina II je imela dva in skupina III en genotip. Največje poprečne vrednosti skupine za premer in maso plodu, pridelek na drevo in število plodov na drevo so bile določene v skupini II, ki ji je sledila skupina I. Med vsemi ge- notipi je bila večja genetska raznolikost ugotovljena pri sortah Zebda, S9 in S10, kar nakazuje, da bi se ti genotipi lahko upora- bili za preučevanje značaja širše variabilnosti, kar bi privedlo do zelo kakovostnih rekombinantnih linij. Ob dejstvu, da je mango izredno heterozigotna kulturna rastlina, bi se ti rezultati lahko uporabili za odbiranje primernih staršev v programih križanja in pri vegetativnem razmnoževanju izbranih lastnosti. Ključne besede: Mangifera indica; genotipi manga; genet- ska variabilnost; analiza glavnih komponent; dednost Acta agriculturae Slovenica, 119/2 – 2023 2 H. ZAKI et al. 1 INTRODUCTION Mango (Mangifera indica L.) is the king of fruits and, most important, occupies second place in terms of cultivated area after citrus in Egypt. The cultivated area of mango trees reached 265509 feddan (0.42 ha), producing 1,091,535 tons of fruits. The fruiting area in Egypt’ s Aswan Governorate, where the current study was conducted, got 13573 fed (5700.66 ha) and generated roughly 67076 tons of fruits (SIAERI, 2019). Mangoes are cultivated in over 100 countries, and the top-producing countries are India, China, Thailand, Indonesia, Mexico, and Nigeria (FAO, 2019). Mangoes are naturally heterogeneous and have a wide range of seed genotypes, demonstrating a wide ge- netic range in shape, color, bearing behaviors, maturation stage, and yield. Several factors, including selection, mu- tation, genetic drift, and recombination, provide sources of genetic diversity. Most mango cultivars, including some superior clones, are hybrids resulting from natu- ral cross-pollination (Krishna & Singh, 2007; Ramírez & Davenport, 2016). Despite the level of genetic diversity among mango landraces and cultivars, many seeding strains have high productivity. Some of them outperform some of the mango varieties in some crop traits. How- ever, in Egypt, wide mango varieties mainly arise from seedling strains. Mango is an allopolyploid, most prob- ably amphidiploid, and outbreeding plant with chromo- some number 2n = 40 (Pierozzi & Rossetto, 2011) and is highly heterozygous as performance varies with the climate and resulting in a high level of genetic diversity. Vasugi et al. (2012) revealed that to develop new vari- eties, breeding programs that use germplasm with spe- cific traits need precise information. Mangos have been classified based on fruit characteristics, including color, size, shape, mass, peel percentage, stone, pulp, and nutri- ent composition (Igbari et al., 2019; Arogundade et al., 2022). The morphological characteristics that distinguish mango cultivars make it difficult to distinguish between closely related varieties (Begum et al., 2016). Abdelsalam et al. (2018) presented some mango cultivars in Egypt by employing morphological properties of the fruits and molecular markers techniques to show the diversity of the collected cultivars. Understanding the variability among a crop’s ge- netic stocks is crucial to breeding programs. Moreover, genetic variability is essential to know the gene source for a particular trait within germplasm to identify desirable cultivars for commercial production and improve yield and other traits (Govindaraj et al., 2015). Also, the pro- gress in breeding programs depends on the genetic vari- ability in the breeding material. Most of the genetic char- acteristics are governed by more than one gene, which is highly affected by the environment. Hence, the coef- ficients of variation (both genotypic and phenotypic) and heritability (the degree to which a trait can be attributed to a particular gene) are crucial in determining the inher- itance pattern of the traits. The heritability of a genetic character is important in determining the response to the selection (Piepho & Mohring, 2007). Because of the great heritability, the breeder can choose plants depending on how they display their traits (Holland, 2014). Majumder et al. (2013) studied 60 mango genotypes to determine their variability, heritability, and genetic advance. They found that significant variations were ob- served in 20 traits. Also, there were considerable differ- ences between the genotypic (GCV) and the phenotypic coefficients of variation (PCV) for almost all the char- acters, indicating the effect of the environment on the expression of these traits. However, among the studied characters, GCV and PCV were high for fruit yield per plant and the number of fruits per tree. All the studied traits showed considerably high heritability, ranging from 56.2 to 98.2 %, while the genetic advance was high for the top traits. Moreover, the combined influence of genetic advance and heritability offers the most effective conditions for selecting a specific trait. Estimating each trait’s contribution to the total ob- served variations in the genotypes is important; this ena- bles the identification of the significant traits accounting for the greater share in the observed variations and then enables the breeder to focus on specific traits of interest for crop improvement. Consequently, the current work aimed to evaluate 11 mango genotypes by employing multivariate analysis based on cluster and principal com- ponent analysis (PCA) for yield and some of its contrib- uting traits, as well as estimating the genetic variability, heritability, and genetic advance among the yield and its components. 2 MATERIALS AND METHODS The present study was conducted on 12 years old mango trees grown on clay soil at Qus, Qena governo- rate, Egypt (25°54’56.2” N 32°45’30.7” E) during two suc- cessive seasons of 2021 and 2022. The experimental ma- terials comprised 11 genotypes, i.e., ten seeding strains and one check as the Zebda variety. The trees were spaced at 7 m x 7 m. The experimental design was intended in Randomized Complete Block Design with three replica- tions. A single tree of both strains and varieties with the same uniform size is considered one replicate. Common cultural practices for orchards were provided with stand- ard agronomic methods such as fertilization, irrigation, and pest management, as usual for mango farms. Data was recorded on ten quantitative characters in three rep- Acta agriculturae Slovenica, 119/2 – 2023 3 Variability of genetic - morphological traits ... of Mangifera indica L. growing in Upper Egypt lications and a single tree considered as replication for the studied traits as follows: yield per tree (Y), number of fruits per tree (NF), fruit mass (FM), fruit length (FL), fruit diameter (FD), fruit pulp (FP), seed mass (SM), to- tal soluble solids (TSS), total sugars (TS g) and total acid- ity (AC). The yield per tree was recorded over the study period, fruit mass was measured by weighing balance, to- tal soluble solids were measured by using a handy refrac- tometer (AOAC, 2000), and total acidity was measured as g citric acid/ 100 g pulp according to (AOAC, 2000). 2.1 STATISTICAL ANALYSIS The mean values of the data were analyzed accord- ing to (Sharma, 1998). Data were analyzed separately for each year and combined over two years (Steel & Torrir, 1980). The differences between the means for all stud- ied traits were calculated using revised L.S.D. at 5 % and 1 %. Genotypic and phenotypic coefficient of variation (GCV and PCV) were computed by the formula suggest- ed by Singh & Chaudhury (1985). Heritability, in a broad sense, was estimated according to Falconer (1989). The genetic advance was calculated as per the formula given by (Allard, 1960). The hierarchical cluster analysis procedure of the program SPSS-V.13 for windows carried out cluster analysis. Principal component analysis (PCA) was per- formed using Minitab statistical software -V .17. The PCA was used to determine the extent of genetic variation. Eigenvalues were obtained from PCA, which were used to determine the axes’ relative discriminative power and associated characters (Pradhan et al., 2015). The geno- types were categorized in a bi-plot figure and compared with the cluster analysis. Simple correlation coefficients between different traits under the study were analyzed by the method of Hayes et al. (1955). 3 RESULTS AND DISCUSSION 3.1 MEAN PERFORMANCE OF MANGO GENO- TYPES As shown in Table 1, it should be called that 2 out of 11 genotypes, i.e., S9 and S10, were superior for the number of fruits per tree, yield per tree, fruit mass, and fruit diameter in the two years and showed significant (p < 0.01) compared to ‘Zebda’ (chick genotype No. 11), which was superior from the other genotypes in 5 out of 10 traits namely, fruit pulp, seed mass, TSS, total sugars, and total acidity in two years. Generally, the genotypes S9 and S10 were superior in yield traits, while ‘Zebda’ was superior in all quality traits. Igbari et al. (2019) evaluated seven mango varieties using 13 morphological traits, and the results exhibited some variability in fruit sizes and shapes, leading to reliable discriminating characters. They demonstrated that while some mango fruit mor- phological traits showed the greatest diversity, others showed little to no variation and could not be effectively employed as a characterization tool. 3.2 ANALYSIS OF V ARIANCE, GENOTYPIC AND PHENOTYPIC COEFFICIENTS OF V ARIATION The individual analysis of variance for each year and the combined analysis are shown in Table 2. The results indicated that mean squares of the studied genotypes were highly significant (p < 0.01) every two seasons and combined, indicating wide genetic diversity among the genotypes for all examined traits. Meanwhile, there were no significant differences in combined analysis among years for all traits except for the number of fruits/tree. However, the interaction of genotypes × years was signif- icant (p < 0.01) for three out of ten studied traits: number of fruits/ tree, yield/ tree, and fruit mass. These results agree with Hamad (2021) and Serry et al. (2019). Table 3 displays the heritability and predicted ge- netic advance, as well as the extent of variability within ten characters across different genotypes, as evaluated by range, genotypic coefficient of variation, and phenotypic coefficient of variation. The highest range of variation was recorded in the number of fruits per tree (141.77- 488.73 and 146.90-496.63 fruits), followed by yield per tree (39.27-137.70 and 40.70 - 141.30 kg/tree), fruit mass (220.13-281.80 and 224.43-285.33 g) in first and sec- ond years, respectively among the characters (Table 3). A moderate range of variation was found in seed mass percentage (6.33-19.10 %) and (19.10-71.82 %), with a mean of 15.11 and 16.70 % in the first and second sea- sons, respectively. The remaining contributing characters had a narrow range of variation, indicating a small value of variability among the genotypes. The results of Jena et al. (2021) showed a marked variation in the fruit traits of mango genotypes, reflecting the highly heterozygous nature. Akhtar et al. (2007) stated that characters with a high range of variation should be prioritized in the selec- tion. Galal et al. (2017) and Patel et al. (2015) obtained a wide range of phenotypic variations, high heritability, and genetic advance among the genotypes for the num- ber of traits. Generally, population variability is essential for breeding programs, as substantial variation in the qualities of interest indicates an opportunity for success- ful improvement through selective breeding. A high magnitude of GCV percentage and PCV Acta agriculturae Slovenica, 119/2 – 2023 4 H. ZAKI et al. Table 1: Means of the studied traits for eleven mango genotypes cultivated in Upper Egypt for the years 2021 and 2022 Genotypes Number of fruits/tree Yield/tree (kg) Fruit mass (g) Fruit length (cm) Fruit diameter (cm) Fruit pulp (%) Seed mass (%) TSS (%) Total sugars (%) Total acidity (%) 1 st Ye ar S1 285.83 ± 15.72 61.23 ± 34.74 220.13 ± 26.17 8.57 ± 0.09 7.3 ± 0.07 62.17 ± 2.76 18.73 ± 0.24 13.93 ± 0.1 10.87 ± 0.44 0.34 ± 0.00001 S2 308.80 ± 51.87 69.8 ± 16.48 230.13 ± 9.77 8.7 ± 0.09 7.5 ± 0.04 61.97 ± 0.44 19.1 ± 0.01 14.17 ± 0.32 10.87 ± 0.25 0.31 ± 0.00003 S3 322.33 ± 46.97 70.63 ± 56.14 236.17 ± 11.32 8.97 ± 0.06 7.67 ± 0.06 62.23 ± 0.32 18.07 ± 0.3 14.83 ± 0.02 11.2 ± 0.12 0.305 ± 0.00003 S4 339.00 ± 25.04 82.07 ± 30.77 248.47 ± 10.17 8.67 ± 0.44 7.63 ± 0.09 62.4 ± 0.39 18.27 ± 0.03 15.33 ± 0.02 11.23 ± 0.02 0.291 ± 0.00001 S5 364.73 ± 37.76 91.50 ± 41.97 257.83 ± 4.42 8.93 ± 0.33 7.77 ± 0.06 63.47 ± 0.08 18 ± 0.21 15.27 ± 0.1 11.47 ± 0.04 0.277 ± 0.00005 S6 378.67 ± 38.58 98.80 ± 10.36 260.1 ± 4.81 9 ± 0.31 7.93 ± 0.06 63.87 ± 0.02 17.1 ± 0.36 15.87 ± 0.04 11.3 ± 0.13 0.275 ± 0.00003 S7 390.43 ± 34.40 102.93 ± 34.54 262.77 ± 25.9 9.43 ± 0.12 7.87 ± 0.2 64.4 ± 0.93 17.4 ± 0.16 15.9 ± 0.04 12.23 ± 0.09 0.257 ± 0.00001 S8 408.83 ± 33.82 107.47 ± 44.33 268.67 ± 10.89 9.57 ± 0.09 8.07 ± 0.09 65.23 ± 0.02 17.2 ± 0.16 16.2 ± 0.04 12.57 ± 0.17 0.25 ± 0.00003 S9 428.17 ± 17.42 120.80 ± 05.32 276 ± 24.25 10.03 ± 0.26 8.13 ± 0.06 66.67 ± 0.3 16.6 ± 0.16 16.23 ± 0.16 12.63 ± 0.02 0.252 ± 0.00001 S10 488.73 ± 19.33 137.70 ± 23.85 281.8 ± 9.25 10.67 ± 0.24 8.37 ± 0.02 68.23 ± 0.6 16 ± 0.17 17.13 ± 0.04 13.43 ± 0.15 0.245 ± 0.00001 Chick 141.77 ± 10.94 039.26 ± 0.96 247.17 ± 52.02 11.9 ± 0.04 7.63 ± 0.06 72.17 ± 0.16 6.33 ± 0.04 17.93 ± 0.143 14.47 ± 0.04 0.32 ± 0.0001 Means 350.66 89.29 253.57 9.49 7.81 64.8 15.11 14.99 11.47 0.26 LSD 0.05 12.97 4.97 4.58 0.38 0.34 1.3 0.7 0.51 0.59 0.05 LSD 0.01 17.68 6.77 6.25 0.52 0.46 1.77 0.96 0.7 0.8 0.07 2 nd Ye ar S1 298.97 ± 13.33 68.6 ± 7.09 224.43 ± 14.16 8.77 ± 0.05 7.23 ± 0.04 62.2 ± 2.01 19.1 ± 0.16 14.53 ± 0.06 10.73 ± 0.24 0.338 ± 0.000112 S2 315.5 ± 22.21 73.2 ± 9.49 238.47 ± 5.97 8.83 ± 0.06 7.4 ± 0.09 62.33 ± 0.44 19 ± 0.25 15.33 ± 0.13 10.8 ± 0.13 0.315 ± 0.000025 S3 326.57 ± 55.44 78.27 ± 7.12 237.23 ± 18.13 9.03 ± 0.02 7.6 ± 0.07 62.13 ± 0.3 18.5 ± 0.16 15.17 ± 0.09 11.07 ± 0.09 0.31 ± 0.0001 S4 347 ± 28.99 88.2 ± 4.69 251.03 ± 7.7 8.97 ± 0.17 7.76 ± 0.06 63.23 ± 0.1 18.2 ± 0.09 15.86 ± 0.06 11.37 ± 0.02 0.295 ± 0.000025 S5 372.63 ± 42.8 94.27 ± 14.06 252.5 ± 23.59 9.13 ± 0.13 7.87 ± 0.1 63.67 ± 0.14 18 ± 0.16 16.1 ± 0.16 11.63 ± 0.003 0.27 ± 0.000025 S6 380.37 ± 35.1 98.5 ± 12.31 258.6 ± 6.31 9.57 ± 0.02 7.8 ± 0.16 64.03 ± 0.49 17.6 ± 0.09 16.03 ± 0.1 11.87 ± 0.04 0.258 ± 0.000004 S7 410.07 ± 36.56 109.37 ± 10.17 265.43 ± 22.66 9.63 ± 0.06 7.9 ± 0.21 65.07 ± 0.44 17.3 ± 0.16 16.33 ± 0.16 12.37 ± 0.2 0.26 ± 0.000025 S8 421.53 ± 27.32 112.5 ± 10.93 269 ± 3.64 10 ± 0.28 7.6 ± 0.39 65.23 ± 0.14 17 ± 0.25 16.47 ± 0.08 12.5 ± 0.01 0.26 ± 0.000025 S9 444.1 ± 19.91 123.63 ± 11.96 275.63 ± 23 10.1 ± 0.36 7.96 ± 0.25 66.93 ± 0.17 16.5 ± 0.04 16.67 ± 0.02 13.13 ± 0.3 0.252 ± 0.00001 S10 496.63 ± 19.88 141.3 ± 31.92 285.33 ± 14.42 11 ± 0.21 8.27 ± 0.08 67.7 ± 0.11 15.77 ± 0.04 17.27 ± 0.02 13.4 ± 0.14 0.250 ± 0.00002 11(chick) 146.90 ± 54.27 40.7 ± 1.11 238.4 ± 15.97 11.53 ± 0.03 7.83 ± 0.01 70.67 ± 0.69 6.7 ± 0.16 17.43 ± 0.13 15.03 ± 0.06 0.323 ± 0.000132 Continued on the next page Acta agriculturae Slovenica, 119/2 – 2023 5 Variability of genetic - morphological traits ... of Mangifera indica L. growing in Upper Egypt Means 360.02 88.72 254.19 9.69 7.75 64.84 16.7 16.11 12.17 0.28 LSD 0.05 7.43 3.8 4.37 0.45 0.42 1.19 0.64 0.34 0.54 0.05 LSD 0.01 10.13 5.19 5.97 0.61 0.57 1.63 0.87 0.46 0.73 0.07 Table 2: Mean squares of variance analyses for the studied traits of eleven mango genotypes cultivated in Upper Egypt for the years 2021 and 2022 and combined analysis for the two years S. O. V df NF Y (kg/tree) FM (g) FL (cm) FD (cm) FP (%) SM (%) TSS (%) TSg (%) AC (%) Ye ar 1 Replications 2 119.09 226.37 121.26 1.73 0.44 0.58 0.2 0.15 0.38 0.001 Genotypes 10 24464.9** 2405.4** 1113.2** 3.14** 0.28** 30** 37.4** 4.3** 4.0** 0.003** Error 20 57.95 8.5 7.24 0.05 0.04 0.58 0.17 0.09 0.12 0.0001 Ye ar 2 Replications 39.18 86.9 96.664 0.79 0.94 0.22 0.14 0.58 0.35 0.001 0.001 Genotypes 25503.8** 2373.4** 1043.2** 2.47** 0.24** 21.57** 36.12** 2.29** 5.10** 0.003** 0.003** Error 19.03 4.99 6.61 0.07 0.06 0.49 0.14 0.04 0.1 0.0002 0.0001 Combined analysis Y ears (Y) 1 1445.8** 292.74 6.37 0.62 0.62 0.02 0.1 2.64 1.82 1.82 Error (a) 4 1264.46 229.82 110.55 1.42 1.42 0.41 0.2 1.02 0.46 0.46 Genotypes (G) 10 27219.3** 4769.1** 2123.5** 5.53** 5.53** 50.93** 73.42** 6.27** 9.02** 9.02** G × Y 10 22749.4** 9.61** 32.82** 0.09 0.09 0.59 0.12 0.27 0.11 0.11 Error (b) 40 2.35 0.57 6.76 0.04 0.04 0.53 0.16 0 0.1 0.1 Acta agriculturae Slovenica, 119/2 – 2023 6 H. ZAKI et al. percentage were observed in the number of fruits per tree, followed by yield per tree and fruit mass in both seasons. Meanwhile, the other traits recorded less differ- ence between GCV and PCV and less influence by envi- ronmental conditions (Table 3). High estimates of broad sense heritability for these variables show little to no en- vironmental influence, even though they exhibit a little mismatch between PCV and GCV , as evidenced by these results. GCV’s high value can be exploited through prop- er selection. Galal et al. (2017) reported that the higher the genotypic coefficient of variation value, the more po- tential for character improvement. These findings agree with Majumder et al. (2012); Patel et al. (2015); Sridhar et al. (2018), and Das et al. (2021). They found significant heritability and genetic advance among the genotypes and tiny variations between the genotypic and pheno- typic coefficients of variation for practically all variables, indicating that environmental influences were minimal. The high PCV and GCV were obtained for fruit mass, seed width, seed mass, acidity, TSS, and yield/plant. The high PCV and GCV were obtained for fruit mass, seed width, seed mass, acidity, TSS, and yield/plant. 3.3 HERITABILITY AND GENETIC ADV ANCE As our understanding of genetics continues to ex- pand, we can utilize heritability to forecast how choos- ing superior genotypes will ultimately pan out. From the results presented in Table 3, the heritability percentage ranged from 75.63 (fruit diameter) to 99.93 % (number of fruits per tree). High heritability percentage estimates coupled with the high genetic advance in the number of fruits per tree (99.76 and 119.09 %) in the first season indicate that the environment less influenced this char- acter, showing that these traits were controlled by a small number of genes or, alternatively, that there was an addi- tive genetic influence even if they were polygenic in na- ture. As this is the case, selecting certain characteristics would be more useful for increasing yield. The high value Table 3: Range of values and genetic parameters for all studied traits of mango genotypes cultivated in Upper Egypt during the years 2021 and 2022 Characters Min Max GCV (%) PCV (%) Hb (%) GA Ye ar 1 Number of fruits/tree 141.77 ± 10.94 488.73 ± 19.33 2320.07 2325.58 99.76 119.09 Yield/tree (kg) 39.26 ± 0.96 137.7 ± 23.85 894.78 897.95 99.65 17.44 Fruit mass (g) 220.13 ± 26.17 281.8 ± 9.25 145.38 146.33 99.35 14.82 Fruit length (cm) 8.57 ± 0.09 11.9 ± 0.04 10.86 11.03 98.46 0.1 Fruit diameter (cm) 7.3 ± 0.07 8.37 ± 0.02 1.03 1.2 85.85 0.07 Fruit pulp (%) 61.97 ± 0.44 72.17 ± 0.16 15.11 15.41 98.08 1.17 Seed mass (%) 6.33 ± 0.04 19.1 ± 0.01 74.69 75.04 99.54 0.35 TSS (%) 13.93 ± 0.1 17.93 ± 0.143 8.84 9.03 97.83 0.18 Total sugars (%) 10.87 ± 0.44 14.47 ± 0.04 10.88 11.21 97.07 0.24 Total acidity (%) 0.245 ± 0.00001 0.34 ± 0.00001 0.35 0.35 99.3 0.0002 Ye ar 2 Number of fruits/tree 146.90 ± 54.27 496.63 ± 19.88 2359.54 2361.3 99.93 39.18 Yield/tree (kg) 40.7 ± 1.11 141.3 ± 31.92 844.32 846.1 99.79 10.26 Fruit mass (g) 224.43 ± 14.16 285.33 ± 14.42 135.93 136.8 99.37 13.53 Fruit length (cm) 8.77 ± 0.05 11.53 ± 0.03 8.27 8.51 97.15 0.14 Fruit diameter (cm) 7.23 ± 0.04 8.27 ± 0.08 0.78 1.02 75.63 0.09 Fruit pulp (%) 62.13 ± 0.3 70.67 ± 0.69 10.84 11.09 97.73 0.99 Seed mass (%) 6.7 ± 0.16 19.1 ± 0.16 71.82 72.11 99.6 0.29 TSS (%) 14.53 ± 0.06 17.43 ± 0.13 4.64 4.73 98.06 0.08 Total sugars (%) 10.73 ± 0.24 15.03 ± 0.06 13.67 13.94 98.07 0.2 Total acidity (%) 0.250 ± 0.00002 0.338 ± 0.000112 0.36 0.36 98.45 0.0004 Genotypic coefficient of variation (GCV), phenotypic coefficient of variation (PCV), heritability (Hb), and genetic advance (GA) Acta agriculturae Slovenica, 119/2 – 2023 7 Variability of genetic - morphological traits ... of Mangifera indica L. growing in Upper Egypt of heritability coupled with a moderate degree of genetic advance was recorded for yield per tree, fruit mass in the two seasons, and the number of fruits per tree in the 2 nd season. Thus, selection would be sufficient in situations of high heritability value and high or moderate value of genetic advance. This condition develops because of the interaction of additive genes (Das et al., 2021). Sridhar et al. (2018) concluded that high heritability implies that the environment’s influence was negligible, allowing the breeder to choose plants based on their phenotypic ex- pression. Hence the selection of the characters would be suitable for improving mango. Because strong heritability does not always reflect high genetic progress, high heritability coupled with a lower degree of genetic advance was seen in the results of fruit length, fruit diameter, fruit pulp percentage, seed mass percentage, TSS percentage, total sugars, and total acidity, demonstrating that environmental factors and non-additive gene effects (dominance and epistasis) played a more significant role in determining these char- acteristics than did additive genetic factors (Sridhar et al., 2018; Getachew et al., 2021). All of the analyzed traits of mango genotypes with high heritability in the Das et al. (2021) study had high genetic advance values, indicating that additive genes controlled these qualities, and that se- lection would favor their improvement. In addition, Jena et al. (2021) concluded that the high heritability of man- go traits and closeness of GCV and PCV values indicate they are less environmentally effective. Consequently, a reliable selection is made for breeding based on pheno- typic characteristics (Bally and De Faveri, 2021). 3.4 PRINCIPAL COMPONENT ANALYSIS AND GENETIC DISTANCE Figure 1 shows the various components and the ei- genvalues calculated by principal components analysis (PCA). The principal component analysis revealed that four principal components, PC1, PC2, PC3, and PC4, with eigenvalues 4.70, 2.12, 0.12, and 0.06, respectively, have accounted for the total cumulative variability among genotypes. The first two principal components, PC1 (67.1 %) and PC2 (30.25 %), showed eigenvalues of more than one, and cumulatively they explained 97.35 % vari- ability (the highest variance when correlating the most relevant components), where the contribution of PC1 towards variability was the highest (67.1 %). The results showed that fruit mass and total sugars in PC1 and fruit mass and number of fruits in PC2 had the highest load- ings. Many authors as Lawson et al. (2019) and Sridhar et al. (2022), established the effectiveness of PCA, proving it could classify mangoes. Lal et al. (2019) reported that PCA for 17 traits of 60 mango genotypes was reduced to six principal components with eigenvalues up to 1.0, presenting a cumulative variance of 78.78 % variation among the genotypes. As shown in Table 4 and Figure 2, PC1 has a positive association with total sugars and fruit mass and a nega- tive association with total acidity. The second PC has a positive association with fruit mass and the number of fruits while the negative association with total sugars. The third PC has a positive association with fruit diam- eter and the number of fruits while a negative association with yield per tree. PC4 has a positive association with fruit mass and a negative association with yield per tree. The current investigation indicated that five major characters contributed one hundred percent to genetic divergence out of a total of seven yield and contributing traits. The number of fruits per tree and the yield per tree were found to contribute 87.8 % and 8.4 %, respectively, to genetic divergence out of the five major traits studied (Figure 3). Previous studies (Rajan et al., 2009; Majumder et al., 2012; Singh, 2016; Sridhar et al., 2022) have also reported the maximum contribution of the number to genetic divergence in mango genotypes. Therefore, the Figure 1: Scree plot of Eigenvalues, variability proportion (PTV), and cumulative variability (CV) for studied traits of eleven mango genotypes Table 4: Principal component analysis for different traits in mango genotype Variables PC1 PC2 PC3 PC4 NF 0.429 0.479 0.515 0.254 Y 0.165 0.0316 -0.254 -0.838 FM 0.627 0.571 -0.054 0.435 FL 0.144 0.0630 -0.092 0.233 FD 0.058 0.240 0.829 -0.278 AC -0.323 -0.239 0.356 0.313 TS g 0.669 -0.719 0.185 0.047 Acta agriculturae Slovenica, 119/2 – 2023 8 H. ZAKI et al. number of fruits would be the critical parameter for se- lecting divergent genotypes. Clusters I and II exhibited the highest cluster mean values for most studied physical traits (Table 5). The highest cluster mean values for fruit diameter, fruit mass, yield per tree, and number of fruits per tree were found in Cluster II, followed by cluster I. Cluster III represented the highest cluster mean value for total acidity, total sugars, TSS, fruit pulp, and fruit length. Although cluster IV had the maximum number of geno- types (4), no remarkable feature was noticed in this clus- ter for most different characters, and it had the lowest mean values for fruit diameter, fruit length, fruit mass, total sugars, total soluble solids, and fruit pulp. In order to decipher the variation among the geno- types, a principal component analysis (PCA) was carried out. Moreover, a scattered diagram of the genotypic dis- tribution pattern on the axis is shown in Figure 4. The scree plot indicates most of the variation is derived from the first and second components in the eigenvalue of the genotypes data. The results of biplot-PCA stated the pres- ence of high genetic variations among genotypes based Figure 2: Scree plot of Eigenvector for studied traits of 11 mango genotypes in Upper Egypt Figure 3: Graphical representation of the proportionate con- tribution of studied major traits towards genetic divergence Table 5: Average (av) of studied traits for each cluster along with standard deviation (SD), as well as the difference (dif) between each cluster, mean, and total mean Cluster No. Fruit diameter (cm) Fruit length (cm) Fruit mass (g) Yield/tree (kg) Number of fruits/tree Total acidity (%) Total sugars (%) TSS (%) Seed mass (%) Fruit pulp (%) I av ± SD 7.86 ± 0.001 9.41 ± 0.11 261.86 ± 34.88 101.91 ± 58.42 390.91 ± 43.39 0.26 ± 0.00003 12 ± 0.25 16.03 ± 0.08 17.45 ± 0.15 64.37 ± 0.56 dif 0.08 -0.18 7.99 10.52 35.56 -0.02 -0.11 0.12 0.79 -0.45 II av ± SD 8.19 ± 0.04 10.46 ± 0.3 279.7 ± 30.03 130.86 ± 49.3 464.41 ± 59.95 0.25 ± 0.00 13.15 ± 0.15 16.83 ± 0.28 16.22 ± 0.22 67.39 ± 0.68 dif 0.4 0.86 25.82 39.46 109.06 -0.03 1.05 0.91 -0.44 2.57 III av ± SD 7.73 ± 0.00 11.72 ± 0.00 242.78 ± 0.00 39.98 ± 0.00 144.33 ± 0.00 0.32 ± 0.00 14.75 ± 0.00 17.68 ± 0.00 6.52 ± 0.00 71.42 ± 0.00 dif -0.05 2.13 -11.1 -51.42 -211.01 0.04 2.65 1.77 -10.14 6.6 IV av ± SD 7.52 ± 0.04 8.82 ± 0.02 235.76 ± 26.82 74 ± 7.93 318 ± 45.06 0.31 ± 0.00029 11.02 ± 0.06 14.9 ± 0.32 18.63 ± 0.18 62.33 ± 0.11 dif -0.27 -0.78 -18.12 -17.4 -37.34 0.03 -1.08 -1.02 1.97 -2.49 Acta agriculturae Slovenica, 119/2 – 2023 9 Variability of genetic - morphological traits ... of Mangifera indica L. growing in Upper Egypt on the data of studied traits (Figure 4). The first and fourth clusters had four genotypes accounting for 72.8 % of total genotypes (36.4 % each), beside two and one genotypes were classified in the second and third clusters accounting for 18.1 % and 9.1 % of total genotypes, re- spectively (Table 6). Pairwise comparisons were conducted between all genotypes, and the mean dissimilarity values were cal- culated based on five traits of the studied mango fruit. The distance between all eleven mango genotypes was evaluated. The Euclidean distance coefficient ranged from 0.539 (between S1 and S2) to 16.334 (between S2 and ‘’Zebda’), where the mean distance between groups was found with a maximum (16.334), as shown in Ta- ble 7, which indicates to a reasonable variance between the genotypes. Zebda cultivar was found to be much dis- tanced genetically from other genotypes (>10 DC), fol- lowed by S10 [from S1 (7.6 DC), S2 (7.5 DC), S3 (7 DC), and S4 (6.3 DC)], S9 [from S1 (6 DC) and S2 (5.9 DC)] as well as both S10 [from S5, (5.4 DC)] and S9 [from S3, (5.4 DC)] that distanced from the genotypes under study. Most other genotypes were scattered over the plot with a medium or close genetic distance. There may have been shared ancestors between the genotypes, as evidenced by the close distance between them and their grouping within a common cluster (Lal et al., 2019). When there is a lot of variance between individuals’ genes, it might cause phenomena known as allelic amplitudes to appear in the population’ s phenotypes. Using varieties from vari- ous clusters with high to moderate genetic distances in crossing programs may be advised to create new recom- binants with desirable characteristics (Majumder et al., 2013). Figure 4: Principal component analysis (PCA) based on the first and second components for the eleven mango genotypes Table 6: Optimization grouping between 11 mango genotypes, obtained by cluster analysis, based on five fruit characteristics, us- ing the Euclidian distance Clusters No. of genotypes Percentage Genotypes included I 4 36.4 % GROUP1 (Y1 > = 0, Y2 > = 0): S5, S6, S7 and S8 II 2 18.1 % GROUP2 (Y1 > = 0, Y2 < 0): S9 and S10 III 1 9.1 % GROUP3 (Y1 < 0, Y2 < 0): Check IV 4 36.4 % GROUP4 (Y1 < 0, Y2 > = 0): S1, S2, S3 and S4 Table 7: Euclidean distance coefficient (DC) among 11 Mango genotypes S1 S2 S3 S4 S5 S6 S7 S8 S9 S10 ‘Zebda’ S1 0 0.539 1.052 1.732 2.34 3.031 3.846 4.483 6.019 7.642 16.329 S2 0 0.855 1.428 2.123 2.852 3.682 4.325 5.91 7.518 16.334 S3 0 0.893 1.631 2.263 3.16 3.805 5.432 7.023 15.625 S4 0 0.831 1.509 2.39 3.032 4.682 6.253 15.085 S5 0 0.798 1.586 2.229 3.858 5.44 14.409 S6 0 1.068 1.66 3.268 4.817 13.641 S7 0 0.647 2.317 3.879 13.057 S8 0 1.702 3.238 12.527 S9 0 1.631 11.268 S10 0 10.085 Acta agriculturae Slovenica, 119/2 – 2023 10 H. ZAKI et al. The hybridization program would be sensible if performed with ‘Zebda’ combined with any other stud- ied genotypes and between S10 with S1, S2, or S3 due to higher observed distances to obtain higher values of es- sential characteristics, as well as a mitigation of the speed of primitive extinction and adaptive genes between geno- types (Govindaraj et al., 2015). Small distances between S1 and S2 (0.539 DC) or S2 and S8 (0.647) may corre- spond to originating from a common ancestor, or some genetic material may be substituted between the parental roots of these genotypes, making them all combined into one main group (Davis, 1997; Tahir et al., 2021). 3.5 UPGMA CLUSTERING DENDROGRAM Figure 5 presents the UPGMA tree diagram gener- ated by cluster analysis based on five fruit traits of mango genotypes. Generally, it shows two large classes: low seed mass (SM) trait (‘Zebda’) and high or medium SM trait (other genotypes). Four groups were formed in a com- plex selection across the approved cut-off point; ‘Zebda’ formed a single cluster within a class with a low SW trait and the other ten genotypes in the other class. Genotypes clustered similarly in the dendrogram, cluster analysis, principal component analysis (PCA) graph, and along the two axes of the PCA graph (Figure 4). Once more, ‘Zebda’ created a single cluster that was very different from the other clusters, suggesting that this genotype could be crossed with others to produce offspring with the desired characteristics. The perusal of the results re- vealed that the number of fruits per tree and fruit mass exhibited higher estimates of GCV, heritability, and ge- netic advance, indicating additive gene effects controlling these traits. Therefore, individual plant selection for these traits would be effective in the mango crop. Accordingly, non-additive control the inheritance of all studied traits except the two above traits (number of fruits per tree and fruit mass); hence, other methods used in the breeding that traits other than selection like hybridization, muta- tions, and vegetative propagation, especially mango is a highly heterozygous crop. The results of genetic studies can be used for the selection of parents in hybridization programs. Hence, direct selection may be followed to im- Figure 5: Dendrogram, using average linkage (Between Groups), for eleven mango genotypes based on five fruit traits Acta agriculturae Slovenica, 119/2 – 2023 11 Variability of genetic - morphological traits ... of Mangifera indica L. growing in Upper Egypt prove mango for these characters. Sridhar et al. (2018) and Das et al. (2021) both find results consistent with these conclusions. 3.6 CORRELATION COEFFICIENTS Understanding how different traits are linked is crucial during the crop improvement selection process (Fasahat et al., 2016). Simple correlation coefficients be- tween different traits in eleven mango genotypes for nine traits in two years (above and below) are demonstrated in Table 8. In the present study, the highest significantly posi- tive correlation coefficients were obtained between yield per tree and number of fruits per tree (0.987 and 0.995), followed by fruit mass (0.966 and 0.971), fruit pulp (0.905 and 0.940), fruit length (0.865 and 0.910) and total sug- ars % (0.819 and 0.911) in first and second seasons, re- spectively. This finding implied that selection procedures aimed at increasing yield per tree would improve these characteristics automatically. On the other hand, seed mass demonstrated a negative and significant correla- tion with each yield per tree (-0.838 and -0.883), no of fruits per tree (-0.860 and -0.954), fruit mass (-0.833 and -0.913) and fruit pulp (-0.850 and -0.868) as well as TSS % (-0.400 and -0.885) and total sugars (-0.802 and -0.913) in first and second seasons, respectively. The number of fruits per tree showed positive and highly significant with fruit mass (0.955 and 0.973), fruit length (0.868 and 0.911), and fruit pulp (0.910 and 0.942), while it demon- strated insignificant with seed mass (-0.860 and-0.954) in first and second seasons, respectively. These results agree with Samal et al. (2012) and Igbari et al. (2019). They used the Pearson correlation coefficient for man- go varieties quality parameters and found positive and negative correlations between many fruit traits. Lawson et al. (2019) also used Pearson’s correlation coefficient to explore the relationship between the postharvest quality parameters during mango fruit ripening. A real picture of the genetic relationships between various traits and the direct and indirect contributions of one trait to another is provided by correlation analysis (Jena et al., 2021). In our investigation, positive and negative correlations between quantitative characteristics were strongly reflected. 4 CONCLUSIONS Eleven genotypes of mango exhibited substantial genetic diversity. The highest range of variation was re- corded in the number of fruits per tree, followed by yield per tree and fruit mass. High heritability estimates cou- pled with a high or moderate degree of genetic advance in the number of fruits per tree, yield per tree, and fruit mass. The correlation was positive and significant be- tween yield per tree, with each of number of fruits per tree, fruit mass, fruit length, fruit pulp, and total sugars. In contrast, seed mass demonstrated a negative and sig- nificant correlation with yield per tree, number of fruits per tree, fruit mass, and fruit pulp in the two years of study. For the future experiment, traits contributing maximum to genetic diversity, such as fruits per tree, fruit mass, and yield per tree, should be prioritized as se- lection parameters, and diverse genotypes identified in the present study may be utilized for attempting heterotic cross combinations and developing hybrid varieties. 5 ACKNOWLEDGEMENT Great thanks and gratitude to Prof. Dr. Ahmed F.A. Table 8: Simple correlation coefficients between each pair of nine traits in 1 st (above diagonal) and 2 nd year (below diagonal) in eleven mango genotypes Traits Y (kg) NF FM (g) FL (cm) FD (cm) FP (%) SM (%) TSS (%) TSg (%) Y (kg) 0.987** 0.966** 0.865** 0.846** 0.905** -0.838** 0.469 0.819** NF 0.995** 0.955** 0.868** 0.847** 0.910** -0.860** 0.466 0.847** FM (g) 0.971** 0.973** 0.773 0.805** 0.850** -0.833** 0.397 0.788 FL (cm) 0.91** 0.911** 0.869** 0.859** 0.817** -0.693 0.473 0.711 FD (cm) 0.649** 0.646 0.637 0.662 0.755 -0.638 0.382 0.627 FP (%) 0.94** 0.942** 0.929** 0.856** 0.546 -0.850** 0.639 0.879** SM (%) -0. 883** -0.954** -0.913** -0.828** -0.595 -0.868** -0.400 -0.802** TSS (%) 0.883** 0.891** 0.901 0.698 0.45 0.808** -0.885** 0.483 TSg (%) 0.911** 0.912** 0.889** 0.745 0.428 0.895** -0.913 0.867** **. The mean difference is significant at the 0.01 level Acta agriculturae Slovenica, 119/2 – 2023 12 H. ZAKI et al. Ebeid, director of the Agricultural Research Station of Al- Marashda, Qena, Egypt, for his continued assistance in this work. 6 AUTHOR CONTRIBUTIONS The study’s planning and design included the par- ticipation of all authors. Mansour, MM, and Osman, SOA, prepared the materials and collected the data; Hussein, NRA, and Zaki H analyzed the data. Mansour, MM, Osman, SOA, and Zaki H wrote the original and subsequent versions of the manuscript. All authors have reviewed and approved the final manuscript. 7 DECLARATIONS 7.1 CONFLICT OF INTEREST The authors declare that they have no conflict of in- terest. 8 REFERENCES Abdelsalam, N. R., Ali, H. M., Salem, M. Z. M., Ibrahem, E. G., & Elshikh, M. S. (2018). Genetic and morphological characterization of Mangifera indica L. growing in Egypt. Hortscience, 53(9), 1266-1270. https://doi.org/10.21273/ hortsci13084-18 Akhtar, M. S., Oki, Y., Adachi, T., & Khan, M. H. R. (2007). 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