Advanced Studies in Biology, Vol. 7, 2015, no. 10, 413 - 422 HIKARI Ltd, www.m-hikari.com http://dx.doi.org/10.12988/asb.2015.5419 Partitioning of Eggplant Cultivars in North Central Nigeria Using Gross Vegetative and Reproductive Characters *C.U. Aguoru, F. Idakwo and J.O. Olasan Department of Biological Sciences, University of Agriculture, Makurdi, Nigeria * Corresponding author Copyright © 2015 C.U. Aguoru, F. Idakwo and J.O. Olasan. This article is distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Eggplants emanating from a gene bank were studied. The aim was to partition and separate the cultivars into species level on the basis of their variable characters. Seeds were obtained from the seed gene bank of the University of Agriculture, Makurdi, Nigeria, and planted in the university research farm. Forty nine (49) cultivars at full maturity were examined using thirty (30) vegetative and thirty three (33 reproductive characters. Among the cultivars, the following characters remained unvaried: bud position (terminal), leaf type (simple), leaf arrangement (alternate), pubescence type (puberulent), venation type (pinnately netted), petal cohesion (fused), ovary position (superior), corolla shape (companulate), anther type (basifixed), filament adhesion (free) and symmetry of flower (actinomorphic). Some characters were moderately varied but not important to separate the cultivars. The prominent variables that formed the basis of partitioning the species are: leaf sizes, leaf shapes, leaf apices, number of leaf produced, plant height, number of days to produce flower, number of days to yield fruit, quantity of fruit produced (yield), fruit sizes, fruit colour, fruit shape, fruit stripe, fruit groove, fruit taste, fruit position, colour of petal and influorescence type. Based on these features, the cultivars are separated into eight (8) different taxonomic groups that may be assigned specific circumscription and named accordingly by taxonomists. Keywords: Eggplant, Partitioning, Vegetative character, Reproductive character, Taxonomy 414 C.U. Aguoru et al. Introduction Family solanaceae is well recognized globally as it contains major indispensable food crops which include; pepper, tomato, potato and eggplant. These crops have contributed immensely towards the global poverty alleviation and hunger reduction (FAO, 2014). Eggplant (Genus Solanum) is a vegetable and fruit crop of wide ecogeographical distributions. However, the genomics of this crop has not been extensively studied when compared with other solanaceous vegetables (Agnieska et al., 2007). Studies on eggplant recently attracted global attention due to its numerous nutritive and medicinal potentials coupled with the diversity in morphological forms. Many authors have criticized and suggested different nomenclatures for different eggplant species based on reports on diversity studies. However, taxonomic difficulties on the crop still persist due to the wide distribution of varying morphological and sometimes confusing types (Agnieska et al., 2007). Interspecific hybridization has been reported to be a major challenge in eggplant studies (Oyelana and Ugborogho, 2008). This is because the overall effect of this natural process is the emergence of varying hybrid complexes that possess unique characters that may be totally different from the parental stock. Hence, the genus Solanum is the most variable among other genera of the solanaceae family (Doganlar et al., 2002; Frary et al., 2003). Therefore, systematic investigation and breeding programmes are vigorously being pursued on eggplant all over the world. Eggplants have been characterized using morphological, phytochemical and molecular evidences (Osei et al.,2010; Chinedu et al.,2011; Mariola et al.,2014; Aguoru et al.,2015abc). Reports have indicated wide variation in major taxonomic characters even within members of a particular species. Aguoru et al. (2015a) used population genetic parameters to reveal the level of genetic polymorphism in eggplant across different populations in Nigeria. They recommended that regions of high polymorphism should sustain this trend as necessary for improvement prorammes. Despite the variation on eggplant reported across the globe, molecular evidences exist that the same genes are conserved as evolution progresses (Doganlar et al., 2002; Frary et al., 2003; Aguoru et al.,2015b). This present study is aimed at partitioning and separating mature eggplant cultivars arising from a pool of germplasm into distinct specific taxa based on their gross vegetative and reproductive taxonomic characters. Materials and Methods Eggplant seeds were obtained from the seed gene bank of the University of Agriculture, Makurdi, Nigeria. They were planted in the school research farm. Forty nine (49) cultivars at full maturity were examined using thirty (30) vegetative and thirty three (33) reproductive characters. Qualitative characters were physically examined while quantitative measurements were done using appropriate instruments. Photographs of the various cultivars were taken. Data were analysed using SPSS software and Microsoft Excel programme. Partitioning of eggplant cultivars in north central Nigeria 415 Results and Discussion In all the cultivars, the following vegetative and reproductive features remained constant and unvaried: stem type (woody), bud position (terminal), leaf type (simple), leaf arrangement (alternate), pubescence type (puberulent), venation type (pinnately netted), petal cohesion (fused), ovary position (superior), corolla shape (companulate), anther type (basifixed), filament adhesion (free) and symmetry of flower (actinomorphic) (table 1). Similarity recorded in these qualitative characters therefore corroborates the molecular gene conservation phenomenon in eggplant as reported by Aguoru et al. (2015b) and Agnieska et al. (2007). The authors opined that irrespective of the significant variations among the various eggplant cultivars, certain traits remain unchanged which tend to unify the species along a common line of ancestry. However, all the cultivars showed tremendous variations in some quantitative traits. Some vegetative traits that are important in demarcating the species include: internode length, leaf sizes, leaf weight, number of leaves produced, stem diameter and plant height (figure 1). S.anguivi was highly differentiated on the basis of its tall height. S.aethiopicum Shum and S.anguivi were noted for producing the highest number of leaves (115). Flower production was fastest in S.aethiopicum Shum (86 days of planting) while the Gilo Kumba complex was the first in producing fruits (95 days). Fruit sizes were largest in S.athiopicum Kumba (9.1cm in diameter). Meanwhile, the highest fruit yield was recorded among three members of S.aethiopicum Shum (53, 36 and 33 fruits per plant) followed by S.anguivi (30 fruits). The last two species were therefore highly yielding in terms of leaf and fruit production though their fruit sizes were relatively tiny. This quantitative approach therefore agrees with the view of Aguoru et al.(2015b) who analysed eggplant seedlings using quantitative trait analysis. In their findings, these traits, which are coded for by polygenes, varied among eggplant species and they could also form the basis of selection by plant breeders (Mariola et al., 2014; Aguoru et al., 2015b). Qualitative inheritance also varied among the cultivars most especially in leaf, fruit and floral characteristics (table 2 and 3). The combination of qualitative and quantitative approach in both vegetative and reproductive features has provided a detailed morphotypic investigation that is sound enough to separate all the species. Previous studies (Osei et al., 2010; Aguoru et al., 2015c ) that reported wide variation among the members of eggplant species based on such gross morphology are strongly supported. The prominent variables that formed the basis of partitioning the species are: leaf sizes, leaf shapes, leaf apices, number of leaf produced, plant height, number of days to produce flower, number of days to yield fruit, quantity of fruit produced (yield), fruit sizes, fruit colour, fruit shape, fruit stripe, fruit groove, fruit taste, fruit position, colour of petal and influorescence type. (figure 1 and 4). On this note, the phylogenetic tree has revealed that the cultivars are separated into eight different species, though some are closely related 416 C.U. Aguoru et al. along a common ancestral lineage while some appeared to be primitive progenitors showing a divergent relationship. This finding therefore agrees with reports of convergent and divergent relationships on eggplant accessions using molecular marker approach (Sifau et al., 2014; Aguoru et al., 2015b). Dendrogram (figure 3) therefore shows that S.anguivi is an old stock of eggplant species which diverged in the course of evolution followed by S.aethiopicum Shum. It has been revealed that these two divergent species yielded the highest number of leaves and fruits though with small fruit sizes. The S.athiopicum Kumba and the unidentified species are more closely related than S,macrocarpon but the three species are related by common ancestry. In the same manner, S.gilo is more closely related to the Gilo-Kumba than the Gilo-Shum hybrid. This confirms that the Gilo-Kumba was a hybrid product of the S.gilo. However, all the eggplant species are well separated and they may be named accordingly. A similar approach of species separation was adopted by Shalom (2011) who used proximate and phytochemical analysis to dermacate S.aethiopicum and S.macrocarpon and concluded that the two species are distinctly different in terms of the quality (types) and quantity of their active ingredients. In conclusion, the roles of gross and total morphological analysis in revealing the phylogenetic relationships among eggplant species cannot be over-emphasized. It forms the basis of all other criteria used in plant taxonomic studies as the characters are easily obtainable, observable and measurable. In this analysis, leaf sizes, number of leaf produced, plant height, number of days to produce flower and fruits, fruit sizes and colours, quantity of fruit yielded and other qualitative and quantitative variables are important features in separating the eggplant species into eight distinct groups. The notable and prominent species that showed traits of interest may be acted upon by plant breeders and growers for continuous propagation or be improved upon. Table 1: Constant characteristics in all species Species S.a Kumba Bud P Leaf T Lf A Pub T Ven T Pet Co Ov P Cor S Anther T Flwr S Fil Ad Term Simple Alt Pubr P/netted Fused Sup Comp Basifixed Reg Free S. a Shum Term Simple Alt Pubr P/netted Fused Sup Comp Basifixed Reg Free S.gilo Term Simple Alt Pubr P/netted Fused Sup Comp Basifixed Reg Free Gilo-Kumba complex Term Simple Alt Pubr P/netted Fused Sup Comp Basifixed Reg Free S.anguivi Term Simple Alt Pubr P/netted Fused Sup Comp Basifixed Reg Free S.macrocarpon Term Simple Alt Pubr P/netted Fused Sup Comp Basifixed Reg Free Gilo-Shum complex Term Simple Alt Pubr P/netted Fused Sup Comp Basifixed Reg Free Unidentified species Term Simple Alt Pubr P/netted Fused Sup Comp Basifixed Reg Free Partitioning of eggplant cultivars in north central Nigeria 417 Legend: T=type Bud P=Bud position; Term=terminal; Pub =Pubescent; Pubr=Puberulent; Ven=Venation; P/netted=Pinnately netted Pet Co=Petal cohesion; Ov P=Ovary position; Sup=Superior; Cor S=Corolla shape; Comp=Companulate; Flwr S= Flower symmetry; Reg=Regular; Fil Ad=Filament adhesion Table 2: Variable vegetative features (qualitative) Species Leaf shape Leaf surface Leaf apex Leaf base Leaf pub Stem Position S.aethiopicum Kumba Cordate/Ovate Rough Cusp/Acc Ob/Tr/Rd P Erect S. aethiopicum Shum Cordate/Ovate Rough/Smooth Cusp/Acc/Acute Ob P/A Erect/Branched Cordate/Obovate Rough/Smooth Cusp/Acute Ob P Erect/Branched Cordate/Ovate Rough Cusp Ob P Erect/Branched S.gilo Gilo-Kumba complex Ovate/Obovate Rough/Smooth Cusp/Acc Ob P/A Erect/Branched Obovate/Cordate Rough/Smooth Cusp Ob/Rd P/A Erect/Branched Gilo-Shum complex Cordate Rough Cusp Ob P Erect/Branched Unidentified species Cordate Rough Cusp/Acc Ob P Erect/Branched S.anguivi S.macrocarpon Legend Cusp/Acc=Cuspidate/Accuminate Ob/Tr/Rd=Oblique/Truncate/Rounded Leaf pub= Leaf pubescence (P=present; A=absence) Table 3: Variable reproductive features (qualitative) Petal colour Infl/type Fruit colour Fruit stripe Fruit groove Fruit shape Fruit position Fruit taste S.aethiopicum Kumba W/C CC White yes/no yes Obl/Obv Int Bt S. aethiopicum Shum W/Cy CC/AX/ST Green yes/no yes Sph/Obl Term/Base Bt/Sw/VBt S.gilo W/C CC/AX Gr/Yel/Wt yes/no yes/no Pyr/Ova/Obv/Obl Term/Base/Int Bt/Sw Gilo-Kumba complex W/C CC White yes/no yes Obv/Ova Int Bt W CC/ST Green no no Rounded Term/Base Bt P/W CC Green yes yes Obl Term Bt Gilo-Shum complex W ST Green yes yes Sph Int Bt Unidentified species W/Wy/C CC/ST NF NF NF NF NF NF Species S.anguivi S.macrocarpon Legend W/C/Cy/Wy/P= white/creamy/cream-yellow/white-yellow/purple Infl/type=Influorescence type (CC/AX/ST=compound cyme/auxillary/solitary) NF= No fruit within 150 days Gr/Yel/Wt= green/yellow/white Sph/Pyr/Ova/Obv/Obl=spheroid/ pyriform/oval/obovate/oblate Term/Base/Int= terminal/base/intermediate Bt/Sw/VBt= bitter/sweet/very bitter 418 C.U. Aguoru et al. 160 140 120 100 80 60 40 20 0 SaKumba SaShum Sgilo Gilokumba Sangv Smacro GiloShum Unid Fig. 1: Some vegetative features of the cultivars IL= Internode length; LL= Leaf length; LB= Leaf breadth; LW= Leaf weight; LS= Leaf shape; LA= Leaf apex; LBASE= Leaf base; LPU= Leaf pubescence; PL= Petiole length; NOL= Number of leaves; STD= Stem diameter; PLTH= Plant height 160 140 120 100 80 60 40 20 Plant Height No of leaves Leaf size 0 Fig.2: Species differentiation on the basis of three important vegetative characters Legend: Sakumba= Solanum aethiopicum Kumba SaShum= Solanum aethiopicum Shum Sgilo= Solanum gilo Gilokumba= Solanum gilo- Solanum aethiopicum Kumba complex Sangv= Solanum anguivi Smacro= Solanum macrocarpon GiloShum= Solanum gilo- Solanum aethiopicum Shum complex Unid= Unidentified species Partitioning of eggplant cultivars in north central Nigeria 419 Fig.3: Phylogenetic relationships to demarcate the cultivars into species 140 120 SaKumba 100 SaShum Sgilo 80 Gilokumba 60 Sangv 40 Smacro 20 GiloShum 0 Unid Fig.4: Floral and fruit features of the cultivars Legend: FL= Flower length; PC= Petal colour; NP= number of petals; NS= number of sepals; LP=length of petal; LS=length of sepal; LF=length of filament; PL= pedicel length; Day F= number of day to flowering; Nsta= number of stamen; FrtL= fruit length; FrtD=fruit diameter; FrtC=fruit colour; Yield= number of fruits produced. 420 C.U. Aguoru et al. 140 120 100 80 Day of flowering 60 Fruit weight 40 Fruit size 20 Yield 0 Fig.5: Species differentiation on the basis of floral and fruit characters. Gilo-Kumba Gilo-Shum S.anguivi S.macrocarpon Partitioning of eggplant cultivars in north central Nigeria 421 References [1] S. Agnieszka, C. Stanshaw, and E. Kunicki, Cultivated eggplants – origin, breeding objectives and genetic resources, a review, Annal of Folia Horticulture, 19 (2007), no. 1, 197-114. [2] C.U. Aguoru, L.O. Omoigui, and J.O. Olasan, Population Genetic Study of Eggplants (Solanum) Species in Nigeria, Tropical West Africa, Using Molecular Markers, International Journal of Plant Research, 5 (2015), no. 1, 7-12. [3] C.U. Aguoru, L.O. Omoigui, and J.O. Olasan, Molecular Characterization of Solanum Species (Solanum aethiopicum Complex; Solanum macrocarpon and Solanum anguivi) using Multiplex RAPD Primers, Journal of Plant Studies, 4 (2015), 1-8. http://dx.doi.org/10.5539/jps.v4n1p27 [4] C.U. Aguoru, L.O. Omoigui, and O.J. Olasan, Characterization of eggplant seedlings using quantitative trait analysis, Scholars Journal of Agriculture and Veterinary Sciences, 2 (2015), no. 1B, 54-60. [5] S.N. Chinedu, A.G. Olasumbo, O.K. Eboyi, O.G. Emiloju, O.K. Arinola, and D.I. Dania, Proximate and plylo chemical analysis of solanum aethiopiccum L and Solanum macro carpen L. fruits, Research Journal of Chemical Sciences, 1 (2011), 63-71. [6] S. Doganlar, A. Frary, M.C. Dauney, R.N. Lester and S.D. Tansley, Conservation of Gene function in the solonaceae as revealed by comparative mapping of domestication trait in eggplant, Genetics, 16 (2002), 1713-1726. [7] FAO Food and Agriculture Organization of the United Nations, 2014. http//faostat fao.org/faostat [8] A. Frary, S. Doganlar, M.C. Daunary and S.D. Tanksley, QTL analysis of morphological trait in eggplant and implication for conservation of gene function during evolution of solananceae species, Theoretical and Applied Genetics, 107 (2003), 359-370. [9] P. Mariola, A. Isabel, V. Santiago, G. Pietro, F. Javier and J. Prohens, Conventional and phenomics characterization provides insight into the diversity and relationships of hypervariable scarlet (Solanum aethiopicum L.) and gboma (S.macrocarponL.) eggplant complexes, Frontier in Plant Science: Journal of Crop Science and Horticultue, 5 (2014), 1-13. http://dx.doi.org/10.3389/fpls.2014.00318 [10] M. K. Osei, B. Banful, C. K. Osei, and M. O. Oluoch, Characterization of African Eggplant for Morphological Characteristics, Journal of Agricultural 422 C.U. Aguoru et al. Science and Technology, 4 (2010), 33-38. [11] O. A. Oyelana, and R. E. Ugborogho, Phenotypic variation of F1and F2 populations from three species of Solanum L. (Solanaceae), Africa Journal of Biotechnology, 7 (2008), 2359-2367. [12] N.C. Shalom, C.O. Abayomi, K.E. Okwuchukwu, C.E. Opeyemi, K.A Olajumoke and I.D. Damilola, Proximate and Phytochemical analysis of Solanum aethiopicum and Solanum macrocarpon fruits in Lagos State, Southwest Nigeria, Research Journal of Chemical Sciences, 1 (2011), no. 3, 1-3. [13] M.T. Sifau, L.A. Ogunkanmi, K.A. Adekoya, B.O. Oboh and T.O. Ogundipe, Partitioning and distribution of random amplified polymorphic DNA (RAPD) variation among eggplant Solanum L. in Southwest Nigeria, International Journal of Genetics and Molecular Biology, 6 (2014), no. 1,1-7. Received: April 17, 2015; Published: October 1, 2015
© Copyright 2026 Paperzz