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Revista Ciência Agronômica

Print version ISSN 0045-6888On-line version ISSN 1806-6690

Rev. Ciênc. Agron. vol.48 no.4 Fortaleza Oct./Dec. 2017

http://dx.doi.org/10.5935/1806-6690.20170077 

Crop Science

Concordance between botanical groups and genetic diversity in peanut1

Concordância entre grupos botânicos e diversidade genética em amendoim

Ingrid Pinheiro Machado2 

Fernanda Helena Oliveira da Silva2 

Renata Fernandes de Matos2 

Tamiris Pereira da Silva2 

Júlio César DoVale2  * 

2Departamento de Fitotecnia, Centro de Ciências Agrárias, Universidade Federal do Ceará/UFC, Fortaleza-CE, Brasil, ingridpin03@hotmail.com, fernandahelena_ufc@hotmail.com, renatafmatos@hotmail.com, tamirisjua@gmail.com, juliodovale@ufc.br

ABSTRACT

The aims of this study were to characterize peanut accessions of germplasm collection of the CCA/UFC and check consistency between the pre-existing botanical groups to estimates of genetic diversity. For this were conducted a trial with 43 accessions of peanut in a randomized block design with three replications. To characterization were used 21 morphological descriptors, where revealed large genetic variation. The mass hundred grains trait showed the main discriminating factors, with relative percentage of 22.1%. The cluster obtained with the linkage complete method, it was possible to view the dendrogram the formation of seven groups based on the Mahalanobis distance. By principal components analysis was identified phenotypic diversity among genotypes. The first three components explained 81% of the total variation. Subsequently, built a three-dimensional scatter chart for access of visualization, eight groups being formed. There was medium magnitude of agreement between the botanical groups and genetic diversity, both by the dendrogram and graphic dispersion proving the dissimilarity between genotypes of different botanic groups. Therefore, crossings between group access botanical Spanish or Valencia with those belonging to the Virginia group should generate segregating populations with high genetic potential.

Key words: Arachis hipogaea L.; Morphological descriptors; Genetics Resources; Conservation

RESUMO

Objetivou-se com esse estudo caracterizar acessos de amendoim da coleção de germoplasma do CCA/UFC e verificar concordância entre os grupos botânicos preexistentes com as estimativas de diversidade genética. Para isso, foi conduzido um ensaio com 43 acessos de amendoim no delineamento em blocos casualizados com três repetições. Para caracterização dos acessos foram utilizados 21 descritores morfoagronômicos, os quais revelaram grande variação genética. O caráter massa de cem grãos se mostrou o principal fator discriminante, com porcentagem relativa de discriminação de 22,1%. Pelo agrupamento obtido com o método de ligação completa, foi possível visualizar no dendrograma a formação de sete grupos com base na distância generalizada de Mahalanobis. Pela análise dos componentes principais também foi constatada grande diversidade fenotípica entre os acessos da coleção. Os três primeiros componentes explicaram 81% da variação total. Posteriormente, foi construído um gráfico tridimensional para visualização da dispersão dos acessos, na qual se verificou a formação de oito grupos. Constatou-se concordância de média magnitude entre os grupos botânicos e diversidade genética, tanto pela classificação observada no dendrograma quanto pela dispersão gráfica, comprovando a dissimilaridade entre acessos de grupos botânicos distintos. Assim, cruzamentos entre acessos do grupo botânico Spanish ou Valência com aqueles pertencentes ao Virginia devem gerar populações-base com elevado potencial genético.

Palavras-chave: Arachis hipogaea L.; Descritores morfoagronômicos; Recursos genéticos; Conservação

INTRODUCTION

All over the world, germplasm banks have been established for the purpose of conserving plant genetic resources (which are invaluable, both presently and in the future), either by conventional methods of genetic improvement or by recent genetic engineering techniques. In this way, plant genetic resources are considered a reservoir in which solutions can be found for various environmental changes, serving as raw material for agricultural development (NASS, 2001).

Active germplasm banks are conservative units of genetic materials with potential for both immediate and future use. They are considered active because are close to the researcher, who performs the exchange of germplasm and frequent plantings for characterization, as well as providing conservation in the short and medium term. However, an active collection of germplasm, to be efficiently used, should have its accessions characterized and evaluated in order to identify the diversity within and between accessions, with all the information available in a computerized system to facilitate the search for users (FREITAS et al., 2011).

Peanut is a rich source of protein and vegetable oil, being consumed worldwide in the most varied forms. The grains of this crop contain approximately 20-25% of high quality protein and 45% of oil (SILVEIRA et al., 2011). About 60% of the world's production is destined for oil extraction, thereby generating industrial by-products used in animal feed while the rest is destined for human consumption in the natural form (SANTOS et al., 2010).

The expansion of the commercial peanut farm in Brazil depends on its technological level and competitiveness, where the availability of productive, profitable and adapted cultivars for the different regions, production systems and market standards is of primary importance (SANTOS, 2010). In this sense, the conservation of collections of accessions, such as the Agricultural Sciences Center of the Federal University of Ceará (CCA / UFC), can support the research on genetic improvement in the search for greater development and adaptation of the culture. This collection was started in 1983 from collections in the state of Ceará, inputs were received from other Brazilian and foreign institutions, mainly from the Senegalese Agricultural Research Institute (ISRA), in Senegal, Africa. Among the Brazilian institutions, the greatest contributions were obtained from the Agronomic Institute of Campinas (IAC), the extinct Agricultural Research Company of Ceará (EPACE) and the National Center for Cotton Research linked to EMBRAPA. The collection has approximately 90 peanut accessions, but little is known about their characterization.

Currently, three botanical groups have been explored in the peanut crop: 1) Spanish, 2) Valencia and 3) Virginia. Genotypes belonging to each of these groups present very striking characteristics that help to differentiate them. However, that does not mean that they are genetically dissimilar. This information is crucial for breeding programs, since the crossbreeding in a breeding program and derived segregant populations are directed to the search for progenies that present gene complementation (MARIM et al., 2009; SUDRÉ et al., 2005). Thus, once the agreement between botanical groups and genetic diversity is established, time can be gained in the breeding process, since there will no longer be a need to make complex evaluations and analyses to identify divergent genotypes.

There are few papers in the literature which address the genetic diversity of peanuts. Also, of the few papers in existence, the vast majority aimed only to evaluate genetic variability, as in the work conducted by Borges, Xavier e Rumjanek (2007), in which were used 29 accessions of peanuts. Others aimed to test different methodologies, in order to group divergent genotypes, as in the work conducted by Ramos et al. (2015), in which 77 accessions of peanuts were evaluated, based on the different methods of grouping. Therefore, no study was identified as linking the botanical groups currently explored with the group formation proposed by diversity analyses.

In this context, the aim of this study was to characterize peanut accessions from the CCA / UFC germplasm collection and to verify the agreement between pre-existing botanical groups and the formation of groups based on estimates of genetic diversity.

MATERIALS AND METHODS

This experiment was conducted at the Federal University of Ceará (UFC), Campus of Pici, in Fortaleza, Ceará, located at 03°47'25" S latitude and 38°30'30" W longitude and an altitude of 21 m. For this, was used a randomized block design with three replications. The treatments consisted of 43 peanut accessions from the CCA / UFC collection (Table 1). Was used a spacing of 0.60 x 0.20 m. Each plot had a total area of 1.8 m2, consisting of a row of 3 m. All the cultural treatments from sowing to harvesting were carried out according to the recommendations of peanut cultivation in the region (BOLONHEZI; GODOY; SANTOS, 2013).

Table 1 Botanical group, genotype, origin and order of registration of the 43 accessions of peanut used in the present study and belonging to the CCA/UFC 

Botanical group Genotype Origin Registration in the CCA / UFC collection
Valencia CE 6811 Ceará EAC-002
TATU Ceará EAC-003
DWARF (M-1) Índia EAC-008
V-4 - EAC-010
GDM Índia EAC-011
A-8 Ceará EAC-015
A-25 Ceará EAC-018
B-8 Ceará EAC-020
B-9 Ceará EAC-021
B-28 Ceará EAC-022
B-34 Ceará EAC-024
Tatu-aéreo Ceará EAC-025
GDM(M1) Ceará EAC-026
HP-2V3mM Índia EAC-027
494 UPL/EPACE EAC-030
1028 UPL/EPACE EAC-034
1066 UPL/EPACE EAC-035
BR-1 Paraíba EAC-105
Spanish 496 UPL/EPACE EAC-038
GEORGIA USA EAC-039
PI 269.689 USA EAC-040
DIXIE-SPANISH USA EAC-041
IAL-18 Bahia EAC-042
PI 165-317 USA EAC-043
TATUÍ IAC/SP EAC-044
J-11 Ceará EAC-045
JH-113 Ceará EAC-046
SPANISH IMPRO USA EAC-048
55-4-37 Senegal EAC-050
MH-1R33/1 Ceará EAC-052
CHICO Senegal EAC-088
GC 337 Senegal EAC-089
841.111 IAC/SP EAC-106
Virginia TMVZNLM Índia EAC-056
MK374 Nigéria EAC-057
SHULAMAH USA EAC-061
GMLM Índia EAC-062
HP-65 - EAC-068
HP-77 - EAC-070
DWARF UPL/EPACE EAC-076
(MI)BELTVILLE UPL/EPACE EAC-077
73-33 Senegal EAC-085
57422 Senegal EAC-086

The check (control) used was the cultivar BR-1, obtained through selection among segregating populations derived from crosses involving parents of the Valencia group, adapted to the conditions of Northeast Brazil. This cultivar presents tolerance to water stress and to cercosporiosis. Moreover, it reaches maturity around eighty days, which makes it one of the most recommended cultivars for the various growing environments in the region.

During the execution of the test, were used the main descriptors of peanut for characterization of the 43 accessions. This information is used, a posteriori, to avoid the conservation of duplicate accessions, as well as to subsidize new breeding programs.

In the vegetative phase, from the 30 days after planting, the following morphological descriptors were evaluated in five plants of the useful area: botanical group; branching type; growth habit; presence of flowers on the main axis; gynophore color; seed color; leaflet color; leaflet format (structure) and leaflet length.

The agronomic characterization was based on the descriptors linked to the crop production components. Data collection were obtained considering the total production of pods of each accession in their respective areas of use. Were measured the other components based on the five plants collected at random. Were adopted the descriptors: cycle; number of days for the appearance of the first flower; number of days to 50% of flowering; plant height; seed / fruit ratio; pod length; number of fruits per plant; percentage of immature fruits; production per plant; mass hundred grains and productivity.

Was performed analysis of variance for each trait and multicollinearity utilized for the identification of possible problems in the residual correlation matrices. Were eliminated the traits that showed multicollinearity at moderate to severe levels. Afterwards, the relative importance of each character for genetic divergence was determined using the methodology of Singh (1981) and the methodology proposed by Garcia (1998) to discard the least important traits.

In the multivariate analyses, the generalized distance of Mahalanobis was used as a measure of dissimilarity and, for the formation of the groups. Were used the complete bonding method and the Tocher optimization method. Were performed all analyses by computational application in Genetics and Statistics GENES (CRUZ, 2013).

Was used the Jaccard coefficient (1901) as the basis for calculating the coincidence index between botanical groups and groups formed by genetic diversity methods (dendrogram and graphic dispersion), determined by equation:

CI=aa+b+c (1)

where: CI = coincidence index; a = value that quantifies the number of coincidence; b = value that quantifies the number of discordance of type 1-0; c = value that quantifies the discordance number of type 0-1.

By adjusting this method, the discordance b and c would be quantified in the same way, thus resulting in a simplified equation:

CIadj=NCNC+NCC (2)

where: CIadj = coincidence index adjusted; NC = Number of coincidence between botanical groups and dissimilarity groups; NNC = number of non-coincidence.

RESULTS AND DISCUSSION

Regarding the morphological descriptors, there was a great variation in the behavior of the CCA/UFC accessions in the peanut collection (Table 2). Approximately 77% of the accessions presented sequential branching, while the others showed branching of the alternate type. This behavior is similar for the presence of flowers on the main axis, with all accessions belonging to either of the botanical groups Valencia or Spanish. The same accessions which had the sequential type of branching, also presented flowers in the main axis, while those with alternating type of branching did not show flowers in the main axis. However, all accessions that expressed this last phenotype are from the Virginia botanical group. According to Alvarez et al. (2005), the sequential branching behavior is typical of the groups Valencia and Spanish, as well as the alternating type that is characteristic of the group Virgínia.

Table 2 Characterization of the 43 accessions of peanut by means of morphoagronomic descriptors 

Registration in the CCA/UFC Type of branching Growth habit Presence of flowers on the main axis Gynophore color Seed color
EAC-002 Sequential Erect Yes Purple Light brown
EAC-003 Sequential Erect Yes Purple Red
EAC-008 Sequential Erect Yes Purple Dark red
EAC-010 Sequential Erect Yes Purple Dark red
EAC-011 Sequential Decumbent-3 Yes Purple Dark red
EAC-015 Sequential Decumbent-3 Yes Purple Red
EAC-018 Sequential Decumbent-3 Yes Purple Red
EAC-020 Sequential Decumbent-3 Yes Purple Light brown
EAC-021 Sequential Decumbent-3 Yes Purple Red
EAC-022 Sequential Decumbent-3 Yes Purple Creme
EAC-024 Sequential Decumbent-3 Yes Purple Red
EAC-025 Sequential Decumbent-3 Yes Purple Red
EAC-026 Sequential Erect Yes Purple Dark red
EAC-027 Sequential Decumbent-3 Yes Purple Cream
EAC-030 Sequential Erect Yes Purple Light brown
EAC-034 Sequential Decumbent-3 Yes Purple Cream
EAC-035 Sequential Decumbent-3 Yes Purple Rosy
EAC-038 Sequential Decumbent-3 Yes Purple Cream
EAC-039 Sequential Erect Yes Purple Light brown
EAC-040 Sequential Decumbent-3 Yes Purple Light brown
EAC-041 Sequential Erect Yes Purple Light brown
EAC-042 Sequential Decumbent-3 Yes Purple Light brown
EAC-043 Sequential Erect Yes Purple Light brown
EAC-044 Sequential Decumbent-3 Yes Purple Light brown
EAC-045 Sequential Decumbent-3 Yes Purple Cream
EAC-046 Sequential Decumbent-3 Yes Purple Cream
EAC-048 Sequential Decumbent-3 Yes Purple Cream
EAC-050 Sequential Decumbent-3 Yes Purple Light brown
EAC-052 Sequential Decumbent-3 Yes Purple Cream
EAC-056 Alternating Decumbent-3 No Purple Spotted rosy
EAC-057 Alternating Erect No Green Spotted rosy
EAC-061 Alternating Procumbent No Purple Spotted rosy
EAC-062 Alternating Decumbent-1 No Purple Spotted rosy
EAC-068 Alternating Decumbent-3 No Purple Light brown
EAC-070 Alternating Decumbent-3 No Purple Spotted rosy
EAC-076 Alternating Erect No Purple Spotted rosy
EAC-077 Alternating Procumbent No Purple Spotted rosy
EAC-085 Alternating Decumbent-3 No Purple Spotted rosy
EAC-086 Alternating Decumbent-3 No Purple Rosy
EAC-088 Sequential Erect Yes Purple Light brown
EAC-089 Sequential Decumbent-3 Yes Purple Light brown
EAC-106 Sequential Erect Yes Purple Light brown
BR-1 (Check) Sequential Erect Yes Purple Red

On the other hand, approximately 60% of the accessions had a decumbent growth habit-3, and 33% presented a growth habit of the erect type, the other 7% were divided between procumbent and decumbent-1. All accessions were classified as precocious or semi precocious, since they closed the cycle between 90 and 110 days.

Precocity (early maturation) and erect/upright stance are highlighted as desirable characteristics for a peanut cultivar to be recommended for the Northeast conditions, since they present important agronomic implications such as greater use of rainfall in short-cycle materials (SANTOS et al., 2013). In this way, the plants spend less time in the field, thus reducing the risk of production losses caused by drought. In addition, cultivars of erect size allow greater densification in the field, in spite of the fact that there is less production per plant, there is a compensatory effect when considering the production area (DUARTE; MELO FILHO; SANTOS, 2013).

The vegetative structure of low-ground peanut accessions (procumbent, decumbent-1 and decumbent-2), which are generally allocated to the Virginia botanical group, allows greater contact of the gynophore with the soil (LUZ et al., 2010; SANTOS; CUSTÓDIO; SANTOS, 2000), a fact also observed in the present study. According to the same authors, upright and semi-erect (decumbent-3) plants have their floriferous buds more distant from the soil, which does not contribute to the reproductive efficiency of the culture.

Most of the morphoagronomic descriptors present qualitative inheritance, i.e., controlled by one or a few genes, with little influence of the environment (ALLARD, 1971). In this sense, since there is variability for these traits, the selection practiced by the breeder may be at the individual level, and should always seek to meet market requirements.

Of all the descriptors, the coloration of the gynophore was the least varied. Only two accessions (EAC-038 and EAC-057) presented the green color of the gynophore, while the others exhibited a purple coloration. However, for the coloring of the seed, there was a variation between light brown, red, dark red, rosy and spotted rosy colors.

In relation to the traits involving the leaflet, there was a predominance of light green coloration, elliptical shape and mean length (Table 3). Was identified a large variation for the number of secondary branches, from an average of 3.4 branches for EAC-042 accessions to 7.1 branches for EAC-057 accessions. The variation was also evident for the number of tertiary branches, with lower mean for EAC-046 accessions and higher for EAC-062. According to Silveira (2010), the increase in the number of secondary and total branches per plant, promotes an increase in the number of gynophores, and these correlate with seed production.

Table 3 Characterization of the 43 accessions of peanuts by means of morphoagronomic descriptors 

Registration in CCA/UFC Leaflet color Leaflet format (structure) Leaflet length Number of secondary branches Number of tertiary branches Cycle
EAC-002 Light green Elliptical Mean 4.6 1.0 90
EAC-003 Light green Elliptical Large 4.6 1.0 90
EAC-008 Light green Elliptical Mean 4.8 - 90
EAC-010 Green Elliptical Mean 4.4 1.3 90
EAC-011 Green Elliptical Mean 5.4 2.0 90
EAC-015 Green Cuneate Mean 4.2 0.5 90
EAC-018 Dark green Elliptical Mean 4.0 0.7 90
EAC-020 Light green Elliptical Mean 4.1 - 90
EAC-021 Green Elliptical Mean 4.5 0.8 90
EAC-022 Green Elliptical Mean 4.2 0.5 90
EAC-024 Dark green Elliptical Mean 4.7 1.5 90
EAC-025 Green Elliptical Mean 4.5 0.8 90
EAC-026 Dark green Elliptical Mean 3.4 - 90
EAC-027 Green Elliptical Mean 4.9 1.6 90
EAC-030 Light green Elliptical Large 4.8 - 90
EAC-034 Dark green Elliptical Mean 5.7 1.4 90
EAC-035 Green Elliptical Mean 5.4 2.8 90
EAC-038 Green Elliptical Little 6.9 4.9 90
EAC-039 Green Elliptical Mean 4.1 - 90
EAC-040 Light green Elliptical Mean 4.8 - 90
EAC-041 Light green Elliptical Mean 5.4 - 90
EAC-042 Light green Elliptical Mean 3.4 1.3 90
EAC-043 Light green Elliptical Mean 5.5 - 90
EAC-044 Green Elliptical Mean 4.4 - 90
EAC-045 Green Elliptical Mean 5.9 3.8 90
EAC-046 Green Elliptical Mean 5.8 0.3 90
EAC-048 Green Elliptical Mean 4.0 0.5 90
EAC-050 Light green Elliptical Mean 4.6 1.0 90
EAC-052 Green Elliptical Mean 3.5 0.7 90
EAC-056 Dark green Lanceolate Little 5.7 11.0 110
EAC-057 Dark green Obovate Little 7.1 7.0 110
EAC-061 Green Elliptical Mean 5.3 10.9 110
EAC-062 Dark green Lanceolate Mean 5.9 11.2 110
EAC-068 Green Elliptical Mean 4.2 - 110
EAC-070 Green Elliptical Little 6.2 9.9 110
EAC-076 Green Elliptical Mean 5.6 7.0 110
EAC-077 Dark green Elliptical Little 5.9 9.2 110
EAC-085 Green Elliptical Mean 6.0 5.1 110
EAC-086 Green Elliptical Mean 5.5 5.0 110
EAC-088 Light green Elliptical Mean 4.0 - 90
EAC-089 Light green Elliptical Mean 4.1 - 90
EAC-106 Light green Obovate Mean 4.9 1.3 90
BR-1 (Check) Light green Elliptical Mean 4.5 - 90

The distinction between botanical groups and their most divergent characteristics is remarkable. For example, Virginia seed has mainly the spotted rosy color, seeds of the Spanish cultivar have the light brown color while that of Valencia has a dark red color. However, in general the analyzed traits also show a positive relationship between the Spanish and Valencia groups, such as growth habit, cycle, and type of branching and presence of flowers on the main stem.

Among the quantitative traits studied, the mass hundred grains was the main discriminant factor among the accessions, with a relative percentage of 22.1% (Table 4). In addition, three other characters presented a great contribution to distinguish between the accessions, including the number of days for the appearance of the first flower, number of days for 50% of the stand to reach flowering, and the percentage of immature fruits, of which the four characters together accounted for 63.9% of the contribution to the divergence.

Table 4 Relative contribution of quantitative traits to genetic diversity according to the methodology proposed by Singh (1981) based on the generalized distance of Mahalanobis, obtained from 43 accessions of peanuts 

Traits Relative contribution
S.j %
Number of days for the appearance of the first flower 7608.7 16.2
Number of days for 50% of the booth to reach flowering 5983.1 12.7
Plant height 3803.4 8.1
Seed / fruit ratio 3905.3 8.3
Pod length 4313.3 9.2
Number of fruits per plant 2004.0 4.3
Percentage of immature fruits 6039.3 12.8
Production per plant 2353.5 5.00
Mass hundred grains 10395.9 22.1
Productivity 618.3 1.3

From the grouping obtained with the complete binding method, were formed eight groups based on the generalized Mahalanobis distance (Figure 1). Group I consisted of accessions EAC-056, EAC-057, EAC-061, EAC-062, EAC-070, EAC-077, EAC-085 and EAC-086. In this, 100% of the accessions are from the Virginia botanical group (Table 1). Group II was formed by only EAC-035, since this accession presented more than 50% level of dissimilarity in relation to group I. Group III was formed by accessions EAC-024, EAC-046, EAC-076, which belong to the groups Valencia, Spanish and Virginia, respectively. Group IV was formed by two accessions, these being EAC-038 and EAC-045, both belonging to the Spanish group.

Figure 1 Dendrogram among 43 accessions of peanut, obtained by the full link method - more distant neighbor, based on the seven most important quantitative traits for genetic dissimilarity 

Were formed groups V, VII and VIII only by accessions of the groups Valencia and Spanish. The following accessions EAC-015, EAC-018, EAC-021, EAC-025, EAC-027, EAC-034, EAC-048 and EAC-052 are present in group V, while group VIII consisted of only one accession, EAC-022, of the botanical group Valencia. Group VI consisted of the other accessions evaluated in the present study and not classified in the aforementioned groups. It is noteworthy that in the latter, there are accessions of the three botanical groups, with 50% belonging to Spanish and 44.44% to Valencia.

According to Sudré et al. (2006), multivariate analysis allows us to make inference about the genetic diversity of genotypes based on several characters simultaneously. Thus, traits that contribute very little to the computation of genetic dissimilarity between genetic materials, should be eliminated from subsequent analyses. The productivity trait, one of the most important, regardless of the culture, contributed least in this sense. Therefore, in order to discriminate efficiently between the accessions of the CCA/UFC collection, the traits related to precocity (early maturation), the number of days for the appearance of the first flower and number of days for 50% of the booth to reach flowering should be considered. This includes traits associated with yield, percentage of immature fruits and mass hundred grains.

Were formed the botanical groups from agronomic classifications based on vegetative and reproductive characteristics that distinguish between subspecies. Thus, genotypes of the Virginia group present the morphological characteristics of representatives of the subspecies hypogaea, var. hypogaea. On the other hand, the groups Valencia and Spanish are denominations of the morphological groups associated with the subspecies fastigiata (fastigiata and vulgaris varieties, respectively). A consequence of this may be the formation of groups V, VI and VII, in which the presence of only or mainly the Spanish and Valencia groups were observed. Probably, the subspecies determined the similarity in the characteristics of the studied accessions. In addition, it was observed that group I formed only by accessions of the Virginia group.

He and Prakash (2001) verified the formation of two main groups among different peanut cultivars, in which an association with the botanical classification was not characterized. In this study, the two groups formed even with the presence of Virginia, Valencia and Spanish as a whole, showed the prevalence of one of the three botanical groups in general. It was observed in the first group that 64.28% of the cultivars belong to the Virginia group while 55.17% belong to the second group (Valencia).

In order to simplify the data set, were obtained the main components in relation to the seven quantitative characters evaluated in peanut accessions. From the estimation of eigenvalues and eigenvectors obtained from the covariance matrix between the standardized values, 71% of the retained variation was observed in the first two components, which somehow justifies the use of a two-dimensional graph (Table 5). However, the three-dimensional graphic dispersion (Figure 2) was chosen to have a notion of "depth", being considered simultaneously as the scores of the first three main components. These results refer to a cumulative variation of 81% with the first three components, since according to Cruz and Carneiro (2006), accumulated variations that add more than 80% in the first main components make possible an analysis through dispersion graphs.

Table 5 Estimates of the variances (eigenvalues) associated with the main components of the seven quantitative traits most important for genetic diversity (1), evaluated in 43 peanut accessions 

Eigenvalue Eigenvalue (%) % accumulated
11.154 49.82 49.82
4.876 21.78 71.61
2.118 9.46 81.07
1.892 8.45 89.52
1.159 5.18 94.69
0.957 4.28 98.97
0.231 1.03 100.00

(1)Mass hundred grains; Number of days for the appearance of the first flower; Percentage of immature fruits; Number of days for 50% of the booth to reach flowering; Pod length; Seed / fruit ratio; Plant height

Figure 2 Graphical dispersion of the scores in relation to the representative axes of the canonical variables (VC1, VC2 and VC3) of 43 peanut accessions 

An inspection of the scores on the chart allowed us to subjectively divide the 43 accessions into eight groups. Group 1: EAC-088, belonging to the Spanish botanical group. Group 2: EAC-026, EAC-039, EAC-040 and EAC-050; in this group, 75% of the accessions belong to the Spanish botanical group while only 25% belong to the Valencia group. Group 3: (EAC-02, EAC-003, EAC-008, EAC-010, EAC-011, EAC-020, EAC-024, EAC-030, EAC-041, EAC-042, EAC-043, EAC-044, EAC-068, EAC-076, EAC-089, EAC-105 and EAC-106). In this group, there are accessions belonging to the three botanical groups, being 52.94% of the accessions of the botanical group Valencia and 35.29% of the Spanish group. Group 4: EAC-025 of the botanical group Valencia. Group 5: EAC-015, EAC-018, EAC-021, EAC-022, EAC-027, EAC-034, EAC-035, EAC-046, EAC-048, EAC-052, EAC-056, EAC-057, EAC-061, EAC-062, EAC-070, EAC-077 and EAC-085. In this group, similar to the third, there are accessions belonging to the three botanical groups, of which the groups Valencia and Virginia have 41.17% each. Group 6: EAC-045 of the Spanish botanical group. Group 7: EAC-038 of the Spanish botanical group, and group 8 with accession EAC-086 of the botanical group Virginia.

For the great majority of accessions, there was coincidence in the formation of the groups by both procedures. The coincidence index adjusted was of medium magnitude when considering both the dendrogram and the graphical dispersion (Table 6). However, the division of groups by the dendrogram presented the most conservative to established botanical groups. This shows that there is an association between botanical groups and those formed by estimates of genetic diversity, that is, accessions belonging to distinct botanical classes tend to be more dissimilar than accessions belonging to the same group. This is due to the different characteristics of each botanical group already established.

Table 6 Coincidence index adjusted between the formation of botanical groups and groups formed by dendrogram procedures and graphic dispersion considering seven quantitative traits evaluated in 43 peanut accessions belonging to the CCA/UFC germplasm collection 

Dendrogram Graphical dispersion
Coincidence
index adjusted
0.628 0.558

According to Souza, Queiróz e Dias (2005), this information can be very useful to breeding programs, since in hybridization activities is evaluated not only the agronomic performance but also the genetic complementarity for the formation of segregating populations. In addition, such information may provide more accurate assessments and analyses in defining the parents for use in breeding programs.

In view of the variability for the various morphological or agronomic traits it was verified a great potential of the accessions pertaining to the collection of the peanut germplasm of the CCA/UFC. This potential refers to the performance of studies aimed at the inheritance or the genetic control of traits and the obtaining of cultivars that may be recommended for the Ceará State in the future. Either way, the breeder must be alert to the requirements of peanut farmers in the state. For this, it is advisable to insert in future crosses, parents who present precocity, upright posture, satisfactory yield per plant, low percentage of immature pods, and adequate productivity (DUARTE; MELO FILHO; SANTOS, 2013).

CONCLUSIONS

  1. The peanut accessions obtained from the CCA/UFC germplasm collection are genetically dissimilar;

  2. The methods of multivariate analysis, generalized distance of Mahalanobis, complete binding and optimization of Tocher, used in this study were efficient to separate the accessions with greater genetic dissimilarity;

  3. There is an agreement of 0.558 for the graphical dispersion and of 0.628 for the dendrogram, between the botanical groups and those generated by the estimates of genetic diversity;

  4. Crossings between accessions of the botanical group Spanish or Valencia with those belonging to the Virginia group should generate segregating populations with high genetic potential;

  5. For the formation of base populations, may be combined alleles of accessions EAC-057 and EAC-062 (Virginia group) with alleles of accessions EAC-025 (Valencia group) or EAC-038 (Spanish group).

1Parte da Monografia da primeira autora apresentada à Universidade Federal do Ceará/UFC

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Received: September 16, 2015; Accepted: February 02, 2017

*Autor para correspondência

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