Evaluation Of Genetic Diversity Research Articles

Assessment of genetic biodiversity and association of micronutrients and agronomic traits using microsatellites and staining methods which accelerates high-micronutrients variety selections within different wheat groups

Evaluation of genetic biodiversity for micronutrients is crucial for breeding high-quality crops and addressing the negative impacts of mineral deficiencies. The objectives of this research were to assess genetic variation and the relationship between grain Fe and Zn levels and agronomic traits in a diverse collection of wheat varieties. Additionally, the study aimed to determine the correlation between microsatellite markers (SSR) and micronutrient quantities. A total of 42 genotypes (Iranian commercial cultivars, landraces, and Afghan and Swiss varieties) were evaluated over a two-year period. Fe and Zn levels were measured using two semi quantitative staining assays and atomic absorption spectrophotometry (AAS) facility. Semi-quantitative staining methods and AAS showed high correlations for micronutrient contents. Landraces exhibited higher Fe (63.79 mg/kg) and Zn (44.76 mg/kg) but lower grain yield compared with commercial cultivars. Heritability estimates ranged 53%-79.43%, suggesting that genetic variance played a higher contribution in the phenotypic variation of traits than environmental factors. Notably, Fe content displayed significant correlations with days to maturity. Canonical correlation analysis (CCA) revealed that Zn content was correlated with four agronomic traits. Evaluation of genetic diversity using SSR markers demonstrated high genetic variation among the genotypes tested. The analysis of polymorphism information content (PIC) indicated that SSR primers had an average PIC of 0.75, with the Xgwm192 primer exhibiting higher PIC than others. Several SSR markers revealed association with micronutrient content that can be used in marker-assisted selection (MAS) programs aimed at selection of high micronutrient genotypes. In conclusion, the findings underscored the substantial genetic diversity present in micronutrient levels among global wheat genotypes, the potential of landraces for micronutrients biofortification of wheat cultivars through cross hybridization, the utility of staining methods for screening high/low micronutrient genotypes, and use of microsatellite markers for marker-assisted breeding aiming to micronutrient improvement in breeding programs.

Evaluation of genetic diversity and genome-wide association studies of resistance to bacterial wilt disease in potato.

The development of novel improved varieties adapted to unstable environmental conditions is possible through the genetic diversity of breeding materials. Potato is among the most important food crops worldwide, however, there are still significant hindrances to breeding gains attributed to its autotetraploid and highly heterozygous genome. Bacterial wilt caused by the Ralstonia solanacearum species complex (RSSC) is an important disease affecting potato among many economically important crops worldwide. No cultivated potato genotypes have shown a satisfactory level of resistance to bacterial wilt. Nevertheless, resistance can play a crucial role in effective integrated disease management. To understand the genetic landscape of bacterial wilt resistance in cultivated potato, we evaluated the diversity of 194 accessions from the International Potato Centre (CIP) using 9,250 single nucleotide polymorphisms (SNPs) and their associations to the response to bacterial wilt disease evaluated over two independent trials. Twenty-four accessions showed high resistance throughout both trials. Genetic diversity analysis revealed three major clusters whose subgroups were mostly represented by CIP clones derived from common parents. Genome-wide association analyses have shown six major hits: two on chromosome 8, and one on each chromosome 2, 4, 5, and 9. These results facilitate genetic dissection of bacterial wilt resistance and marker-enabled breeding in elite genotypes for potato breeding initiatives.

A tip of the iceberg: genome survey indicated a complex evolutionary history of Garuga Roxb. species

Background Garuga Roxb. is a genus endemic to southwest China and other tropical regions in Southeast Asia facing risk of extinction due to the loss of tropical forests and changes in land use. Conducting a genome survey of G. forrestii contribute to a deeper understanding and conservation of the genus.ResultsThis study utilized genome survey of G. forrestii generated approximately 54.56 GB of sequence data, with approximately 112 × coverage. K-mer analysis indicated a genome size of approximately 0.48 GB, smaller than 0.52GB estimated by flow cytometry. The heterozygosity is of about 0.54%, and a repeat rate of around 51.54%. All the shotgun data were assembled into 339,729 scaffolds, with an N50 of 17,344 bp. The average content of guanine and cytosine was approximately 35.16%. A total of 330,999 SSRs were detected, with mononucleotide repeats being the most abundant at 70.16%, followed by dinucleotide repeats at 20.40%. We conducted a preliminary ploidy assessment using Smudgeplot and observed a clear bimodal distribution in G. forrestii at 1/2 relative coverage depth and total coverage depth (2n), suggesting a potential diploid genome structure. A pseudo chromosome of G. forrestii and a gemone of Boswellia sacra were used as reference genome to perform a primer population resequencing analysis within three Garuga species. Principal component analysis (PCA) indicated three distinct groups, but genome wide phylogenetics represented conflicting both between the dataset of different reference genomes and between maternal and nuclear genome.ConclusionIn summary, the genome of G. forrestii is small, and the phylogenetic relationships within the Garuga genus are complex. The genetic data presented in this study holds significant value for comprehensive whole-genome analyses, the evaluation of population genetic diversity, investigations into adaptive evolution, the advancement of artificial breeding efforts, and the support of species conservation and restoration initiatives. Ultimately, this research contributes to reinforcing the conservation and management of natural ecosystems, promoting biodiversity conservation, and advancing sustainable development.

Evaluation of Agronomic and Genetic Diversity in M2V1 Generation of Marigold (Tagetes erecta L.)

Marigold (Tagetes erecta L.) is an ornamental plant widely used as a potted or cut flower due to its vibrant colors and diverse flower shapes. High genetic diversity is essential for successful breeding programs aimed at developing superior varieties. Genetic information can be obtained by estimating variance components and heritability values, key parameters in plant breeding. A high heritability value suggests that genetic factors influence a plant's characteristics more than environmental factors. This study assessed the genetic diversity and performance of vegetative propagation from 2nd generation mutant plants (M2V1). The research was conducted at the Pasir Sarongge experimental field in Cianjur Regency from July to October 2023, using a randomized complete block design with 17 genotypes and three replicates. The genotypes included 14 from vegetative propagation of M2V1 mutant plants and three comparison varieties: “Maharani”, “BAIP 2”, and “BAIP 3”. Data analysis was performed using PKBT-STAT 3.1 software, followed by the honest significant difference (HSD) test at the 5% level. The results revealed significant differences among genotypes in plant height, stem diameter, canopy width, leaf width, flower weight, flower diameter, number of flowers per plant, total flower weight per plant, and flower stalk length. Floret types observed were either all ligulate or all tubuligulate, with flower colors ranging from orange to yellow to white. Traits such as canopy width, flower weight, flower diameter, and stalk length, which exhibited broad genetic diversity and high heritability, can be used for selection in future marigold breeding programs.

Evaluation of Genetic Diversity in Physical and Agronomic Traits of Seven Chickpea Cultivars under Optimum Moisture and Low-Irrigation Conditions

Evaluation of Genetic Diversity in Physical and Agronomic Traits of Seven Chickpea Cultivars under Optimum Moisture and Low-Irrigation Conditions

MORPHOLOGICAL AND YIELD-RELATED POMOLOGICAL CHARACTERIZATION OF INTRODUCED OLIVE (OLEA EUROPEA) CULTIVARS IN RAINFED AREA OF POTHOWAR PUNJAB

This study aims at pomological characterizing of 09 olive cultivars planted in the field area of Barani Agricultural Research Institute (BARI), Chakwal to estimate genetic variability in Ottobratica, Hamdi, FS-17, Gerboi, Arbequina, Persia, Nabali, Koroneiki and Earlik. Following pomological traits: fruit and stone weight (g), fruit and stone size (cm), fruit and stone shape index (length/width) and flesh to stone ratio were studied. Data for studied traits were collected in 2019 according to the International olive council descriptor. A significant genetic difference was noticed in the morphological characteristics of both fruit and stone. Different pomological characters were expressed by each cultivar. A wide range of variation was noticed in fruit weight (1.33-5.57g), stone weight (0.20-0.63g) and flesh/stone ratio (0.90-4.96). Based on their fruit shape, studied cultivars were classified into two groups i.e., ovoid and elongate. However, no significant difference was recorded for the stone shape, as all the studied cultivars had the same elongated stone shape. Concerning the fruit size, high fruit size (4-6g) was observed in FS-17, Hamdi, Earlik and Persia whereas Koroneiki, Nabali and Gerboi had the smallest ones (>2g). Based on our results, Earlik, Hamdi and FS-17 are suggested to be more appropriate for table olive production. Thus, an evaluation of genetic diversity through this study can help in the varietal development of olive for table and oil purposes.

Does decline and recovery process affect clonal and genetic diversity of a coastal plant population?

The evaluation of genetic diversity is important for the conservation of species. However, changes in genetic diversity during conservation are complex processes that depend on the characteristics of the species and environment. To evaluate the changes in genetic diversity from decline to recovery, we surveyed the coastal herb Calystegia soldanella in areas with varying degrees of non‐coastal plant invasion. First, to evaluate genetic diversity before the conservation measures, the spatial clonal structure of adults was investigated in a population invaded by non‐coastal plants. Second, to evaluate genetic diversity after the conservation measures, the regenerated individuals were investigated in the restoration plot. Moreover, to predict future genetic diversity without conservation measures, the effects of non‐coastal plant invasion on the production and genetic diversity of seeds were investigated using individuals from areas with various levels of non‐coastal plant invasion. In the adult population, 16 genets were identified in an 80 m × 4 m area. The maximum genet size was 30.3 m, suggesting the importance of clonal reproduction for population maintenance. In the restoration plots comprising 10 m × 10 m × 3 replicates, many seedlings (1.14 ramets/m2) emerged, resulting in high clonal diversity compared to that of the adult population. Therefore, the biomass and genetic diversity were rapidly restored at the beginning of the conservation practice. Non‐coastal plant invasion did not affect the genetic diversity of the seeds. However, it significantly reduced seed production. This suggests that non‐coastal plant invasion reduces sexual reproduction, resulting in the long‐term loss of genetic diversity.

Reduced representation sequencing reveals weak genetic differentiation between Canadian and European Larus hyperboreus (Glaucous Gull)

Abstract Climate change poses a significant threat to Arctic ecosystems. Evaluation of genetic diversity within and differentiation among populations is needed to effectively conserve Arctic species and ensure genetic variation is appropriately managed. This research examined population genetic structure in Larus hyperboreus (Glaucous Gull), a circumpolar Arctic species that is declining in parts of its range. Population genetic information is needed to help delineate management units, including information on genetic differences among related species, among subspecies (currently distinguished by subtle morphometric and plumage differences), and among colonies in North America. We conducted double-digest restriction site-associated DNA sequencing for 62 L. hyperboreus, 18 L. argentatus smithsonianus (American Herring Gull), 6 L. a. argentatus (European Herring Gull), and 15 L. glaucescens (Glaucous-winged Gull) sampled across the Canadian and European Arctic. Interspecific analyses using 2,145 loci were unable to distinguish members of this species complex. Despite the geographic distance among sampling locations, molecular assignments and principal coordinates analyses based on 621 loci uncovered only weak population genetic differentiation among sampled European and Canadian colonies of L. hyperboreus. As L. hyperboreus occupying the eastern Canadian Arctic appear to be acting as a single panmictic population, conservation plans that protect Arctic habitat may help slow or reverse population declines. Proactive conservation strategies will benefit both L. hyperboreus and associated coastal Arctic ecosystems.

Molecular Identification Validates Morphological Identification of Javanese Cardamom from Banyumas in Central Java, Indonesia

Cardamom is one of the prominent plants with significant economic value in the Banyumas Regency, Central Java, Indonesia. Although Javanese cardamom is traditionally categorized under Amomum compactum, the morphological variations observed create ambiguity about its exact species status. DNA barcoding using the maturase K (matK) and ribulose-bisphosphate carboxylase (rbcL) genes is proven as a reliable technique to elucidate the taxonomic status of morphological variable plant cultivars. This study aimed to characterize cardamom from Banyumas Regency using morphological and molecular approaches for taxonomic status identification and genetic diversity evaluation. The matK and rbcL genes were selected as genetic markers and sequenced using a bidirectional sequencing technique. Morphological examination showed significant color variations at the cardamom stem base. All samples had high genetic identities to reference species in databases and were supported by high query cover and zero e-values. Therefore, molecular characterization, alongside geographic distribution assessment, established that this plant belongs to a single species, Amomum compactum. Additionally, the analysis conducted showed a low level of genetic diversity, as evidenced by haplotype and nucleotide diversity. Low-level genetic diversity provides additional data to convince that cardamon in Banyumas Regency belongs to a single species. These results are essential data in seed selection for further cultivation.

Development of SSR Markers and Evaluation of Genetic Diversity of Endangered Plant Saussurea involucrata.

The conservation biology field underscores the importance of understanding genetic diversity and gene flow within plant populations and the factors that influence them. This study employs Simple Sequence Repeat (SSR) molecular markers to investigate the genetic diversity of the endangered plant species Saussurea involucrata, offering a theoretical foundation for its conservation efforts. Utilizing sequencing results to screen SSR loci, we designed and scrutinized 18 polymorphic microsatellite primers across 112 samples from 11 populations in the Bayinbuluke region. Our findings reveal high genetic diversity (I = 0.837, He = 0.470) and substantial gene flow (Nm = 1.390) among S. involucrata populations (China, Xinjiang), potentially attributed to efficient pollen and seed dispersal mechanisms. Principal Coordinate Analysis (PCoA) indicates a lack of distinct genetic structuring within the Bayinbuluke populations. The cluster analysis using STRUCTURE reflected the genetic structure of S. involucrata to a certain extent compared with PCoA. The results showed that all samples were divided into four groups. To safeguard this species, we advocate for the in situ conservation of all S. involucrata populations in the area. The SSR markers developed in this study provide a valuable resource for future genetic research on S. involucrata.

Evaluation of genetic diversity and population structure for anaerobic germination under saline submergence condition using hypervariable SSR markers in a diverse set of global rice accessions

Evaluation of genetic diversity and population structure for anaerobic germination under saline submergence condition using hypervariable SSR markers in a diverse set of global rice accessions

Genetic diversity evaluation of Luculia yunnanensis, a vulnerable species endemic to Yunnan, Southwestern China based on morphological traits and EST-SSR markers.

Luculia yunnanensis is a vulnerable species endemic to Yunnan Province, Southwestern China, which has high ornamental value. Its wild population has not been fully protected and utilized for a long time, which is not conducive to the long-term stable development of this species. Genetic diversity assessment is the basis and prerequisite for the conservation of rare species. In this study, 21 phenotypic traits and 17 highly polymorphic EST-SSR markers were used to analyze the genetic diversity and genetic structure of 164 individuals from six L. yunnanensis populations. The coefficient of variation of 21 phenotypic traits ranged from 11.76% to 52.58% (mean=21.72%), and the coefficient of variation of 18 traits was less than 30%. The average values of Ne, I, Ho and He were 1.710, 0.619, 0.384, and 0.352, respectively. The genetic diversity of LLO (Ho = 0.476 and He = 0.426) and LCM (Ho = 0.424 and He = 0.381) populations in Lushui County was highest. The GDX populations (Ho = 0.335 and He = 0.269) isolated by Gaoligong Mountain had the lowest genetic diversity. The AMOVA results showed that 13.04% of the genetic variation was among populations and 86.96% was within populations. The average phenotypic differentiation coefficient of phenotypic traits among populations was 18.69%. The results of phenotypic and genetic variation analysis were consistent, indicating that the most of variation exists within population. Genetic structure, UPGMA clustering and PCA analysis results showed that the populations of L. yunnanensis had obvious geographical divisions, and the populations distributed in the southern region and distributed in the northern region of the Nujiang River clustered into one group respectively. Combining the results of phenotypic and molecular markers, we recommend that give priority to the protection of LLO, LCM and GDX population, in order to ensure the sustainable utilization of L. yunnanensis germplasm resources.

Evaluation of genetic diversity among olive trees (Olea europaea L.) from Jordan.

This study aimed to identify and evaluate the genetic diversity of olive trees in Jordan, a country located in the eastern Mediterranean, where olive domestication originated. For this purpose, a total of 386 olive trees were analyzed, including 338 collected from two surveys (JOCC-1 and JOCC-2) across seven regions, and 48 selected accessions from the Olive Germplasm Bank of Jordan (JGBOC). These trees underwent comprehensive phenotypic and molecular characterization using different tools. Significant differences in morphological traits were detected among tested regions using the Chi-square test. Principal components analysis revealed that fruit color change and growth habit as the most discriminating traits, segregating the trees into two groups, with the first group including the Kanabisi cultivar and the second group including the Kfari Baladi cultivar. Utilizing Kompetitive Allele Specific PCR assay, two sets of informative SNPs were used for the genetic diversity analysis. Cladograms were constructed using the maximum likelihood method, revealing a consistent pattern where two clades containing identical genotypes were observed to cluster with the Kfari Baladi or Kanabisi. In addition, the SNP data was used to perform a comparative analysis with the Worldwide Olive Germplasm Bank of Córdoba, which revealed 73 unreported olive genotypes from Jordan. Genetic structure analyses using Discriminant Analysis of Principal Components (DAPC) identified four clusters with distinctive patterns of relatedness among 149 unique accessions, including 52 olive accessions from various Mediterranean countries (IOCC-3). ADMIXTURE analysis revealed four genetic clusters, consistent with the clustering observed in DAPC and cladogram analysis, indicating a high level of genetic admixture among Jordanian olive germplasm. In conclusion, the results show that olive trees in Jordan are highly diverse, providing valuable information for future conservation and management plans.

Evaluation of genetic diversity and population structure of the Chinese chestnut (Castanea mollissima) by using NR-SSR markers

Evaluation of genetic diversity and population structure of the Chinese chestnut (Castanea mollissima) by using NR-SSR markers

Evaluation of genetic diversity using simple sequence repeat markers and analysis of cross compatibility in hydrangeas

AbstractHydrangeas with large inflorescences are widely used as cut flowers and in floral arrangements. However, the genetic diversity of commercially grown hydrangeas has been limited owing to the breeding focus on popular species. Therefore, this study was conducted to suggest interspecific breeding strategies for expanding the genetic diversity in Hydrangea L. by evaluating genetic diversity in the seven main species collected in Korea and analyzing cross compatibility via intra- and interspecific hybridization. Interspecific diversity evaluation using simple sequence repeat markers resulted in the segregation of 35 varieties accounting for seven species into five groups as follows: (1) Hydrangea paniculate group, (2) Hydrangea arborescnes group, (3) Hydrangea anomala and Hydrangea aspera group, (4) Hydrangea quercifolia group, and (5) Hydrangea macrophylla and Hydrangea serrata group. Cross compatibility was confirmed via intra- and interspecific crossing, and hybrids were obtained in 18 crossing combinations. Intraspecific hybrids tend to be easy to obtain, but interspecific hybrids are difficult to obtain due to a variety of factors. While most of the interspecific hybrids were obtained using ovule culture, the crossing between H. macrophylla and H. serrata created hybrids from seed sowing, indicating that H. serrata is a subspecies of H. macrophylla. Bilateral and unilateral incompatibilities were observed across the obtained hybrids. Particularly, weak bilateral compatibility was observed between H. serrata and H.paniculata. Accordingly, it was proposed that hybrids between H. macrophylla and H. serrata can be successfully used as parental materials in crossing with H. paniculata to improve cold tolerance. In addition, cross compatibility was improved in interspecific crossing using H. macrophylla and H. arborescens as maternal plants. It is anticipated that these finding will help improve the genetic diversity in commercial hydrangeas.

Phylogeography and genetic structure of Papaver bracteatum populations in Iran based on genotyping-by-sequencing (GBS)

Papaver bracteatum, known for its high thebaine content and absence of morphine, has emerged as a promising alternative to opium poppy for codeine production. In this study, our objective was to create a diverse panel representing the natural variation of this species in Iran. To achieve this, we employed genotyping-by-sequencing to obtain genome-wide distributed single-nucleotide polymorphisms (SNPs) for phylogeographic analysis, population structure assessment, and evaluation of genetic diversity within P. bracteatum populations. A total of 244 P. bracteatum individuals from 13 distinct populations formed seven genetic groups, along with one highly admixed population. We observed a clear split between the populations inhabiting the Alborz Mts. in the east and Zagros Mts. in the west. In between these mountain ranges, the population of Kachal Mangan exhibited a high degree of genetic admixture between both genetic groups. At or after the end of the last glacial maximum, when climate conditions rapidly changed, all P. bracteatum populations experienced a strong demographic bottleneck reducing the already small effective population sizes further before they increased to their recent strengths. Our results suggest that the ongoing climate change together with human pressure on the species’ habitats and limited seed-dispersal ability are potential factors contributing today to rising genetic isolation of P. bracteatum populations. Our results provide genetic data that can be used for conservation measures to safeguard the species’ genetic diversity as a resource for future breeding approaches in this medicinally important species.

Assessment of the genetic diversity and population structure in Moringa oleifera accessions using DNA markers and phenotypic descriptors

Moringa (Moringa oleifera Lam.) is one of the multipurpose trees with significant promise as a high-value crop of industrial importance, having nutritional, therapeutic, and prophylactic properties. Genetic diversity is a cornerstone of any crop improvement program and plays a key role in the selection of promising parental lines for hybrid breeding. Morphological and molecular markers have been proven to be potential tools for the evaluation of genetic diversity, crop genetic improvement, and conservation of plant genetic resources. In the current study, morphological descriptors, RAPD, and SCoT markers were used to determine genetic diversity among 28 M. oleifera accessions. Significant morphological variations were noted for several economic traits across the accessions studied. Four primary clusters were visible on the dendrogram based on phenotypic markers, indicating clustering of accession from a shared geographical habitat. No correlation was estimated between morphological traits, indicating an environmental influence. Three RAPD and seven SCoT primer sets produced 37 and 46 markers, with 53.2 and 71.3% polymorphisms, respectively. Based on genotypic data and the UPGMA approach, all 28 accessions were separated into two major clusters in the phylogenetic tree, irrespective of any geographical areas. The clustering pattern indicates widespread plant species and rapid gene flow through cross-pollination in Moringa populations. Three subpopulations of the involved accessions were identified by population structure analysis; however, there was only a weak link with the location of plant cultivation. The expected heterozygosity for the three subpopulations varied from 0.23 to 0.32, as per R-based structural analysis. AMOVA's attribution of 86% and 19% of all variations to within- and between-populations, respectively, indicates that there has been gene flow across geographic regions. The PCA showed a wide distribution of genotypes in the scatterplot, also suggesting huge genetic variation among the M. oleifera population. The study revealed a significant level of genetic diversity among M. oleifera accessions, which can be harnessed to conserve plant genetic resources and develop high-yielding, nutrient-dense Moringa cultivars.

Evaluation of genetic variation and host resistance to wheat stem rust pathogen (Puccinia graminis f. sp. tritici) in bread wheat (Triticum aestivum L.) varieties grown in Türkiye.

Wheat stem rust, which is caused by Puccinia graminis f. sp. tritici (Pgt), is a highly destructive disease that affects wheat crops on a global scale. In this study, the reactions of 150 bread wheat varieties were evaluated for natural Pgt infection at the adult-plant stage in the 2019-2020 and 2020-2021 growing seasons, and they were analyzed using specific molecular markers to detect stem rust resistance genes (Sr22, Sr24, Sr25, Sr26, Sr31, Sr38, Sr50, and Sr57). Based on phenotypic data, the majority of the varieties (62%) were resistant or moderately resistant to natural Pgt infection. According to molecular results, it was identified that Sr57 was present in 103 varieties, Sr50 in nine varieties, Sr25 in six varieties, and Sr22, Sr31, and Sr38 in one variety each. Additionally, their combinations Sr25 + Sr50, Sr31 + Sr57, Sr38 + Sr50, and Sr38 + Sr57 were detected in these varieties. On the other hand, Sr24 and Sr26 were not identified. In addition, many varieties had low stem rust scores, including a large minority that lacked Sr57. These varieties must have useful resistance to stem rust and could be the basis for selecting greater, possibly durable resistance.

Evaluation of Genetic Diversity in Gmelina arborea Roxb. Across Different Regions of Gujarat, India: The First Report

Evaluation of Genetic Diversity in Gmelina arborea Roxb. Across Different Regions of Gujarat, India: The First Report

Evaluation of Genetic Divergence among Different Okra Genotypes

Mahalanobis D2 statistics were used to analyse the genetic divergence of thirty different okra genotypes, and the results showed that there was a significant amount of genetic variety. The clustering, inter and intra-cluster distances, and trait contributions provided insights into the genetic variability and diversity within the studied okra population. Thirty diverse genotypes were grouped into five clusters with the highest of eighteen genotypes in the cluster I, five in the cluster III & V and one each genotype in the cluster II and IV. Inter and intra cluster D2 values ranged from 8.00 to 16.7 and 0.0 to 7.4, respectively. It showed that inter cluster distance was higher than the intra cluster distance indicating wide genetic diversity among the genotypes of different groups. The cluster means of 11 characters among five clusters indicated that high genetic variability ranged present for yield per plant (222.1-253.1), number of fruits per plant (31.8-38.9), plant height (59.0-100.7) and days to fifty percent flowering (42.8-54.0). The per cent contribution of yield and its attributing characters in genetic divergence were reported maximum for number of fruits per plant (46.4%) and first fruit node (16.3%). The genotypes HB-691-08, HBT-49-1, Hisar Unnat, Hisar Naveen, HBTC-6-7-1, Varsha Uphar, Arka Abhay were superior for overall yield and yield attributing characters. These genotypes were used to exploit genetic variation for further breeding programme.