Morphometric Characterization of Coconut Germplasm Conserved at Bari

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International Journal of Sustainable Agriculture 4 (3): 52-56, 2012 ISSN 2079-2107 IDOSI Publications, 2012 DOI: 10.5829/idosi.ijsa.2012.04.03.313 Morphometric Characterization of Coconut Germplasm Conserved at Bari 1 1 1 2 M.D. Sarkar, S. Choudhury, N. Islam and M.N. Islam 1 Department of Horticulture, Sher-e-Bangla Agricultural University, Dhaka-1207, Bangladesh 2 Horticultural Research Centre, Bangladesh Agricultural Research Institute, Gazipur, Bangladesh Abstract: An experiment was conducted at the Pomology Research Field, HRC of BARI, Gazipur, Bangladesh during the period from September 2011 to February 2012 to evaluate the morphometric characterization of coconut germplasm. PCA revealed that days to spathe opening, days to male phase and number of nuts per palm contributed for 66.73% of the observed variation. Twenty seven entries of coconut were grouped into 7 clusters. The largest cluster VII included 9 palms, cluster VI, V and II included 8, 4 and 3 palms respectively while cluster I, III and IV included 1 palm. The inter-cluster values were maximum in between clusters III and VII (82.455) while it was minimum in between II and IV (22.351). The intra-cluster distance was maximum in cluster VII (13.210) while the clusters I, III and IV showed no distance. So, the clusters between III and VII could be used as germplasm for future breeding. Key words: Morphometric characterization % Coconut germplasm INTRODUCTION exploiting advantages of natural diversity for crop improvement. Hence, an initial study on the diversity of Coconut (Cocos nucifera L.) is a monocotyledonous coconut of the country is essential for documenting the plant species belonging to the family Palmaceae genetic diversity of coconut in Bangladesh. Therefore, the (Arecaceae), subfamily Cocoideae and the monospecific study was undertaken for characterization and evaluation genus Cocos [1]. It is widely distributed throughout the of coconut germplasm. tropics between 20 N and 20 Slatitude covering about 11.6 million hectares over 86 countries [2]. MATERIALS AND METHODS Asia and the Pacific produce 85 % of the total world coconut production. Bangladesh produces about 100 The experiment was conducted at the Pomology million nuts annually weighing about 90,000 tons in an Research Field, Horticulture Research Centre of area of 30,000 hectares [3]. About 80% of coconut in Bangladesh Agricultural Research Institute (BARI), Bangladesh consumed as fresh fruit and tender nut for Gazipur under the agro-ecological zone of Modhupur drink purpose. Only 9 % is available for processing in oil Tract (AEZ No. 28) during the period from September 2011 mills [3]. to February 2012. Soil of the experimental field was silty Coconut palm is capable of sequestrating clay loam in texture and acidic in nature. Coconut carbon-dioxide and causing soil bio-diversification of germplasm were collected from different Agro Ecological farm product and nutrient recycle. It is a food source Zone of Bangladesh which was planted at BARI campus which provides supplement for body fluids and minerals. in 1998-2001 among which 27 palms of different Bangladesh hardly can produce 5000 tons of coconut oil population was selected. Coconut palms were about 10 against its yearly demand of 30,000 tons [3]. The yield of years. Data on bole category, stem, leaf, flowers and nut nut in Bangladesh is very low on an average 21 nuts per were recorded and subjected to diversity analysis by palm per year as compared to many other coconut SPSS-12 computer packages. Principal component growing countries in the world [3]. Tall type cross analysis (PCA) and clustering were carried to assess the pollinated coconut is grown in Bangladesh for its long pattern of morphological variation. To assess the productive life and nut quality. Collection, conservation relationships within genotypes or classes of the and evaluation of germplasm offer an opportunity of population, a dendrogram was developed. Corresponding Author: S. Choudhury, Department of Horticulture, Sher-e-Bangla Agricultural University, Dhaka-1207, Bangladesh. 52

RESULTS AND DISCUSSION From the resulting dendrogram in 1-5 scale measurement (Fig. 1), the populations were grouped into Principal Component Analysis (PCA): To examine the seven clusters, which were presented in the Table 3. The relationship among quantitative variables, principal cluster VII was the largest, containing nine palms followed component analysis (PCA) was carried out. First three by cluster VI, which included 8 palms. Cluster V consisted components contributed 66.73% of the observed variation of 4 palms while cluster II included 3 and cluster I, III and (Table 1). The rest of the components contributed for IV represents 1 palm (Table 3). Similarity in many 33.27% of variation. phenotypic characters of the genotypes brought them in In Prin1, number of nuts per palm and number of nuts a particular group. The observed diversities in the per bunch contributed to the highest loading 87% collections might be resulted from natural and human followed by 77%, 66% and 58% for girth of peduncle, intervention [4]. number of female flowers and length of central axis of Average intra and inter cluster distance of seven inflorescence respectively. In Prin2, girth at stem clusters were presented in Table 4. The magnitude of intra contributed highest loading 83% followed by 82% and cluster distances indicated the extent of genetic diversity 59% for girth at bole and width of leaflet respectively among genotypes within the cluster whereas inter cluster (Table 2). Contributions of characters towards divergence distances depicted the extent of diversity among were estimated through canonical variate analysis. genotyped between the clusters. It was reported that The coefficients pertaining to the different characters in clusters with lesser magnitude of divergence showed the first two canonical roots presented in Table 2. The instability, while widely divergent clusters remained positive absolute values of the two vectors revealed that distinct in different environments [5-7]. days to spathe opening, days to male phase, number of The higher value of inter cluster distances than intra nuts per palm, number of nuts per bunch, length of central cluster distances indicated that diversity presents more in axis of inflorescence, number of spikelets per between clusters that within clusters. Genetically distant inflorescence, number of female flowers and girth of parents usually able to produce higher heterosis [8-12]. peduncle had the greatest contribution to genetic Keeping this in view, the findings from the present study divergence. On the other hand, the negative absolute indicated that the maximum inter-cluster distance was values of vector-1 and positive absolute value for obtained in between clusters III and VII (82.455) indicated vector-2 for the characters of Girth at bole, Girth at stem, the wider genetic divergence between these two clusters. Width of leaflet and Width of petiole indicated the It was followed by the distance between the clusters I and responsibility of secondary differentiation. III (72.894), III and IV (70.825), III and V (58.362), II and III (64.855). It was observed that, the cluster III had the Cluster Analysis highest distance from the rest indicated that the genotype Number of Clusters and Cluster Members: Twelve in the cluster III was distinctly different from others. variables of 27 palm collections were selected on the basis Parental material selection from these clusters would give of principal component analysis subjected to Unweighted high manifestation of heterosis as well as wide spectrum Paired Group Method Arithmetic Average (UPGMA) for of variation when they are hybridized. Endang et al. [13] cluster analysis using SPSS. stated that the clustering pattern could be utilized in Table 1: Eigenvalues of the Covariance Matrix of 10 principal components for quantitative characters of coconut population Eigenvalues Difference Variance (%) Cumulative (%) PRIN1 3.400 0.765 28.336 28.336 PRIN2 2.635 0.662 21.955 50.290 PRIN3 1.973 0.906 16.443 66.734 PRIN4 1.067 0.160 8.892 75.626 PRIN5 0.907 0.045 7.561 83.187 PRIN6 0.862 0.362 7.184 90.371 PRIN7 0.500 0.161 4.165 94.537 PRIN8 0.339 0.109 2.829 97.365 PRIN9 0.230 0.144 1.917 99.282 PRIN10 0.086 0.06 0.718 100.000 Prin = Principal component 53

Table 2: Eigenvector of 12 characters in the first three Principal Component Variable PRIN1 PRIN2 PRIN3 Days to spathe opening 0.114 0.570-0.781 Days to male phase.0114 0.570-0.781 Number of nuts per palm 0.870 0.013-0.159 Number of nuts per bunch 0.870 0.013-0.159 Length of central axis of inflorescence (cm) 0.578 0.172 0.250 Number of spikelets per inflorescence 0.434 0.359 0.292 Number of female flowers 0.661 0.092 0.423 Girth of peduncle (cm) 0.770 0.239 0.192 Girth at bole (cm) -0.310 0.823 0.294 Girth at stem (cm) -0.299 0.834 0.145 Width of leaflet (cm) -0.152 0.596 0.467 Width of petiole (cm) -0.317 0.178 0.116 Prin = Principal component Table 3: Cluster grouping of 27coconut population Cluster Number Palm Number Total Genotypes I 22 1 II 2, 8, 17 3 III 25 1 IV 24 1 V 13, 14, 18, 21 4 VI 1, 3, 9, 12, 20, 23, 26, 27 8 VII 4, 5, 6, 7, 10, 11, 15, 16, 19 9 Table 4: Intra and inter cluster distances among the various clusters of coconut population Cluster I II III IV V VI VII I 0.00 26.021 72.894 16.808 16.204 49.530 25.014 II 12.910 64.855 22.351 24.226 37.471 23.486 III 0.00 70.825 58.362 27.690 82.455 IV 0.00 23.896 46.903 18.435 V 11.550 35.654 33.177 VI 4.472 56.378 VII 13.210 Table 5: Intra-cluster means for 12 characters of coconut population Cluster number ----------------------------------------------------------------------------------------------------------------------------------- Characters I II III IV V VI VII Days to spathe opening 31.00 34.33 30.00 33.00 31.50 32.00 43.55 Days to male phase 31.00 34.33 30.00 33.00 31.50 32.00 43.55 Number of nuts per palm 40.00 38.33 50.00 20.00 23.75 31.87 33.33 Number of nuts per bunch 8.00 7.67 10.00 4.00 4.75 6.87 6.67 Length of central axis of inflorescence (cm) 70.00 53.33 29.00 36.00 34.50 50.00 45.33 Number of spikelets per inflorescence 37.00 48.00 43.00 31.00 40.00 40.87 38.77 Number of female flowers 109.00 82.00 45.00 15.00 42.50 30.75 39.22 Girth of peduncle (cm) 17.00 15.00 13.00 10.00 11.50 13.25 13.44 Girth at bole (cm) 150.00 128.33 170.00 150.00 150.75 147.50 153.77 Girth at stem (cm) 96.00 85.00 99.00 91.00 91.50 92.25 96.11 Width of leaflet (cm) 5.40 4.93 5.00 4.00 5.00 4.72 4.80 Width of petiole (cm) 3.00 3.10 3.20 3.00 3.20 3.32 3.24 54

V and minimum of 128.33 cm in cluster II. The cluster mean of 99.00 cm was highest for girth at stem in cluster III followed by 96.11 cm in cluster VII, 96.00 cm in cluster I and least of 85.00 cm in cluster II. Cluster means 109.00 for the number of female flowers was highest in cluster I followed by 82.00 in cluster II, 45.00 in cluster III and minimum of 15.00 in cluster IV. In cluster IV, number of nuts per palm, number of nuts per bunch and number of female flowers were minimum for 20, 4 and 15 respectively. CONCLUSION Fig. 1: Dendrogram using average linkage between the conserved genotypes at BARI PCA and cluster analysis revealed that inflorescence and nut characters are the most important components contributing to the observed variation. So, nut yield and quality improvement in coconut would be achieved through selection of these characters. But these collections not yet reached in full bearing stage. So, further studies should be conducted to evaluate the nut characters, bearing habit and yield of selected entries of coconut. choosing parents for cross combinations which likely to REFERENCES generate the highest possible variability for effective selection of various economic traits. 1. Uhl, N.W. and J. Dransfield, 1987. Genera Palmarum. Parents for hybridization could be selected on the Allen Press. Lawrence, Kansas, pp: 491-493. basis of large inter-cluster distance for isolating useful 2. FAO, 1998. Production yearbook for 1997. Food and recombinants in the segregating generations. Increasing Agriculture Organization of the United Nations, parental distance implies a greater number of constraining Rome, 51: 50. alleles at the desired loci and then to the extent that these 3. BBS (Bangladesh Bureau of Statistics), 2002. loci recombing in the F 2 and F 3 generations, following a Statistical Year Book of Bangladesh 1998. Bangladesh cross of distantly related parents, the greater will be the Bureau of Statistical Division, Ministry of Planning opportunities for successful selection for any character of and Evaluation, Government of the People s Republic yield interest [14]. of Bangladesh, pp: 668. The minimum distance was obtained in between 4. Foale, M.A., 1992. Coconut Diversity: Present clusters II and IV (22.351) indicated that the genotypes knowledge and future research needs. pp. 48-58. In: belonging to these clusters were comparatively less coconut genetic resources. Paper of the IBPGR diverse. Thus crossing of genotypes from these two Workshop on Coconut Genetic Resources, Cipanas, clusters may not produce high level of heterotic Indonesia, 8-11 October 1991. International Crop expression in the F 1 s and broad spectrum of variability in Network Series No. 8. IPGRI, Rome, Italy, pp: 41-47. segregating (F 2) population. The maximum intra-cluster 5. Somayajulu, P.L.N., A.B. Joshi and B.R. Murty, 1970. distance was in cluster VII (13.210) while the clusters I, III Genetic divergence in wheat. Indian J. Genet., and IV showed no distance because each of them 30(1): 47-58. included only one palm in each cluster (Table 4). 6. Raut, V.M., V.S.P. Rao, V.P. Patel and G.B. Deodikar, Girth at bole, girth at stem and number of female 1985. Genetic divergence in Triticum durum. Indian J. flowers in all the clusters were found to contribute Genet., 45: 141-151. maximum diversities (Table 5). The cluster mean of 170.00 7. Singh, D., P. Kumar and B.P.S. Chandan, 1980. cm was recorded maximum for girth at bole in cluster III Genetic diversity for some quantitative characters in followed by 153.77 cm in cluster VII, 150.75 cm in cluster barley. Indian J. Genet., 40(2): 391-395. 55

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