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Optimum environment number for the national sunflower trials network

ABSTRACT.

This work aimed to present the optimum environment number methodology and propose the optimization of the National Sunflower Trials Network, by means of the environments exclusion that do not provide loss of the environmental variability already established. Grain and oil yield data of 16 genotypes evaluated at 16 environments of the National Sunflower Trials Network, obtained from trials conducted out-of-season in 2012 and 2013 were used. An analysis was proposed to establish the optimum environment number for genotypes evaluation, based on genotype performance in the various environmental combinations. The removal or maintenance of environments in the experimental network was dynamic, since different environmental combinations impacted the representativeness of the complete network in a different way. This analysis also provides a graphical view of the impact of the environment removal from the network. Once detected points below the established correlation, the researcher could infer about the network minimum environment number and, suggest through consistent information of several testing years, the environment exclusion.

Keywords:
Helianthus annuus L.; environmental stratification; experimental network.

Introduction

Sunflower (Helianthus annuus L.) is an annual plant, diploid (2n = 34), alogamous and native to North America (Kaya, Jocic, & Miladinovic, 2012Kaya, Y., Jocic, S., & Miladinovic, D. (2012). Sunflower. In S. Gupta (Ed.), Technological innovations in major world oil crops (p. 85-129). New York, NY: Springer.). Considered as one of the most important oil plants in the world, more than 90% of its oil production is destined for human consumption (Jocic, Miladinovic, & Kaya, 2015Jocic, S., Miladinovic, D., & Kaya, Y. (2015). Breeding and genetics of sunflower. In E. Martínez-Force, N. T. Dunford, & J. J. Ans Salas (Eds.), Sunflower: chemistry, production, processing, and utilization (p. 1-27). Springfield, IL: AOCS Press.). The crop presents important agronomic aspects such as broad range of drought, cold and heat tolerances (Leite, Brighenti, & Castro, 2005Leite, R. M. V. B. C., Brighenti, A. M., & Castro, C. (2005). Girassol no Brasil. Londrina, PR: Embrapa Soja.), seeds with about 40% of high quality oil and 25% of protein, besides being rich in fiber and possessing low caloric content (Paniego et al., 2007Paniego, N., Heinz, R., Fernandez, P., Talia, P., Nishinakamasu, V., & Hopp, H. E. (2007). Sunflower. In C. Kole (Ed.), Oilseeds: genome mapping and molecular breeding in plants (p. 153-177). Berlin, GE: Springer.).

The main objectives of sunflower breeding are related to obtaining stable cultivars with higher grain and oil yield for use in the production of feed and oil extraction for human consumption (Nobre, Resende, Brandão Junior, Costa, & Morais, 2012Nobre, D. A. C., Resende, J. C. F., Brandão Junior, D. S., Costa, C. A., & Morais, D. L. B. (2012). Desempenho agronômico de genótipos de girassol no norte de Minas Gerais. Revista Agro@mbiente On-line, 6(2), 140-147. DOI: 10.18227/1982-8470ragro.v6i2.781
https://doi.org/10.18227/1982-8470ragro....
). In Brazil, hybrids and sunflower varieties developed in different programs have been evaluated for grain and oil yield by the National Sunflower Trials Network, coordinated by Embrapa. The network established in different Brazilian states, investigates the interaction between genotypes and environments (G x E interaction) and enables the recommendation of adapted genotypes to the different regions. Selection and recommendation of adapted genotypes to the producing regions, tends to increase the success of the crop, providing greater economic return (Porto, Carvalho, Pinto, Oliveira, & Oliveira, 2009Porto, W. S., Carvalho, C. G. P., Pinto, R. J. B., Oliveira, M. F., & Oliveira, A. C. B. (2009). Adaptabilidade e estabilidade de genótipos de girassol para a região subtropical do Brasil. Ciência Rural, 39(9), 2452-2459. DOI: 10.1590/S0103-84782009005000207
https://doi.org/10.1590/S0103-8478200900...
).

According to Ribeiro, Daros, Caires, and Vasconcellos (2011Ribeiro, M. F. S., Daros, E., Caires, E. F., & Vasconcellos, M. E. C. (2011). Desempenho agronômico da cultura do girassol em diferentes condições edafoclimáticas do Sudeste paranaense. Bragantia, 70(3), 550-560. DOI: 10.1590/S0006-87052011000300010
https://doi.org/10.1590/S0006-8705201100...
), experimental networks establishment in different stations throughout the country has been fundamental for the cultivars recommendation and agricultural zoning of the crop, as well as providing information about the yield potential in the different regions. The experimental network makes it possible to identify the GxE interaction, since it gathers information from many trials. The interaction significance allows the study of two optics, the first of them, through adaptability and stability analyzes to study genotype behavior throughout the different environments (Grunvald et al., 2014Grunvald, A. K., Carvalho, C. G. P., Oliveira, A. C. B., Pires, J. L. F., Carvalho, H. W. L., & Oliveira, I. R. (2014). Adaptabilidade e estabilidade de híbridos de girassol convencional e alto oleico na Região Sul do Brasil. Revista Ciência Agrária, 57(3), 217-223. DOI: 10.4322/rca.ao1270
https://doi.org/10.4322/rca.ao1270...
). Or, in an environment point of view, it is possible to perform the decomposition of the interaction in its simple and complex fractions according to the proposition of Cruz and Castoldi (1991Cruz, C. D., & Castoldi, F. L. (1991). Decomposição da interação genótipos x ambientes em partes simples e complexa. Ceres, 38(219), 422-430.) and then to stratify environments into groups whose interaction was at most, simple.

However, in situations where the environments are quite heterogeneous, stratification is difficult, and it is not possible to reduce expenses in breeding programs. Thus, a complementary and inverse methodology to environment stratification, based on the optimal environment number, could be applied in an experimental network to reduce the tests performed. The initial idea is to consider all environments clustered and carry out the environment removal, one by one, to form smaller groups, involving a reasonable number of possible analyzes to be carried out with appropriate computational resources. The different environmental combinations would be tested by means of a statistic, such as the mean or the Pi statistic of Linn and Binns (1988Lin, C. S., & Binns, M. R. A. (1988). A superiority measure of cultivar performance for cultivar x location data. Canadian Journal of Plant Science, 68(1), 193-198. DOI: 10.4141/cjps88-018
https://doi.org/10.4141/cjps88-018...
) and plotted against a pre-established quality value. This value would be the correlation established a priori with the complete experimental network. From the dimensioning of this optimal number, it would be possible to infer which environments could be excluded or maintained in an experimental network and what would be the implication when reducing the number of environments analyzed, as well as observing the consistency of genotype recommendation.

This work aimed to present the optimum environment number methodology and propose the optimization of the National Sunflower Trials Network, by means of the environments exclusion that do not provide loss of the environmental variability already established.

Material and methods

Grain and oil yield (kg ha-1) data from 16 genotypes (Table 1) evaluated at 16 environments of the National Sunflower Trials Network (Table 2), coordinated by Embrapa, obtained from trials conducted out-of-season in 2012 and 2013 were used. The experiments were carried out in randomized blocks with four replicates. The plots consisted of four lines of six meters in length each, with a useful area corresponding to the two central lines, eliminating 50 cm at the ends. The cultural dealings were carried out according to the recommended for the culture.

Joint analysis of variance were performed, considering the effect of genotypes as fixed and of environments, random, according to Equation 1.

Table 1
Identification, name and, classification of sunflower genotypes evaluated in the National Sunflower Trials Network.

Table 2
Environment description of the National Sunflower Trials Network, in the out-of-season of 2012 e 2013.

Yijk=μ+B/Ejk+Gi+Ej+ij+eijk(1)

where:

Yijk is the genotype value of the k-th block, evaluated in the i-th genotype and j-th environment; µ is the overall average of the trials; B/Ejk is the effect of the block k within the environment j; Gi is the effect of the i-th genotype; Ej is the effect of the j-th environment; GEij is the effect of the interaction of genotype i with the environment j; eijk is the experimental error associated with observation Yijk, with eijk ~N (0; σ²).

Since G x E interaction was detected, it was decomposed according to the method proposed by Cruz and Castoldi (1991Cruz, C. D., & Castoldi, F. L. (1991). Decomposição da interação genótipos x ambientes em partes simples e complexa. Ceres, 38(219), 422-430.), which allows to estimate the simple and complex G x E interaction fractions (Cruz, Regazzi, & Carneiro, 2012). The environments where the percentage of the complex interaction did not exceed 50% were considered similar.

In addition to the environmental stratification, we proposed an analysis to establish the optimum environment number, aiming at a greater use of resources in an experimental network. The procedure consisted in the establishment of a classification criterion of the performance of genotypes considering all the environments of the network, based on the Pi statistic of Linn and Binns (1988Lin, C. S., & Binns, M. R. A. (1988). A superiority measure of cultivar performance for cultivar x location data. Canadian Journal of Plant Science, 68(1), 193-198. DOI: 10.4141/cjps88-018
https://doi.org/10.4141/cjps88-018...
) and, later, evaluation of this same performance with a smaller number of environments, in all possible combinations (exhaustive search) given by k=i=2nCnI, in which n is the number of environments evaluated. In the present study, k = 65,519 analyzes were performed.

The optimal environment number would be the one that presented the same agreement, according to a minimum correlation level of 90%, with the performance obtained with all the environments of the network. All analyzes were performed using the software Genes (Cruz, 2013Cruz, C. D. (2013). GENES - a software package for analysis in experimental statistics and quantitative genetics. Acta Scientiarum. Agronomy, 35(3), 271-276. DOI: 10.4025/actasciagron.v35i3.21251
https://doi.org/10.4025/actasciagron.v35...
).

Results and discussion

Individual analyzes of variance revealed a significant effect of genotypes (p < 0.01) for both traits in most environments, showing available genotype variation (Table 3). The coefficients of variation were lower than 20%, compatible with those found for the culture (Porto, Carvalho, Pinto, Oliveira, & Oliveira, 2008Porto, W. S., Carvalho, C. G. P., Pinto, R. J. B., Oliveira, M. F., & Oliveira, A. C. B. (2008). Evaluation of sunflower cultivar for central Brazil. Scientia Agricola, 65(2), 139-144. DOI: 10.1590/S0103-90162008000200005
https://doi.org/10.1590/S0103-9016200800...
; Grunvald et al., 2014Grunvald, A. K., Carvalho, C. G. P., Oliveira, A. C. B., Pires, J. L. F., Carvalho, H. W. L., & Oliveira, I. R. (2014). Adaptabilidade e estabilidade de híbridos de girassol convencional e alto oleico na Região Sul do Brasil. Revista Ciência Agrária, 57(3), 217-223. DOI: 10.4322/rca.ao1270
https://doi.org/10.4322/rca.ao1270...
). The municipalities of Planaltina and Muzambinho stood out for their high average values for both traits and, in Palmas it was where the lowest averages occurred. These results indicate that the different edaphoclimatic conditions affect crop yield. The environments that returned the highest averages are those where there is commercial sunflower cultivation, mainly in the out-of-season (Leite & Borba Filho, 2014Leite, R. M. V. B. C., & Borba Filho, A. B. (2014). Ata - XX reunião nacional de pesquisa de girassol. Londrina, PR: Embrapa Soja.).

Joint analyzes of variance showed significant effect of genotypes, environments and G x E interaction (p < 0.01) for both traits studied (Table 4), showing available genotype variation and environmental diversity, as well as the differential behavior of genotypes throughout the environments, as observed by Grunvald et al. (2014Grunvald, A. K., Carvalho, C. G. P., Oliveira, A. C. B., Pires, J. L. F., Carvalho, H. W. L., & Oliveira, I. R. (2014). Adaptabilidade e estabilidade de híbridos de girassol convencional e alto oleico na Região Sul do Brasil. Revista Ciência Agrária, 57(3), 217-223. DOI: 10.4322/rca.ao1270
https://doi.org/10.4322/rca.ao1270...
) and Porto et al. (2009Porto, W. S., Carvalho, C. G. P., Pinto, R. J. B., Oliveira, M. F., & Oliveira, A. C. B. (2009). Adaptabilidade e estabilidade de genótipos de girassol para a região subtropical do Brasil. Ciência Rural, 39(9), 2452-2459. DOI: 10.1590/S0103-84782009005000207
https://doi.org/10.1590/S0103-8478200900...
), facts that justify the environmental stratification. The coefficients of variation were also compatible with those found for the culture (Porto et al., 2008Porto, W. S., Carvalho, C. G. P., Pinto, R. J. B., Oliveira, M. F., & Oliveira, A. C. B. (2009). Adaptabilidade e estabilidade de genótipos de girassol para a região subtropical do Brasil. Ciência Rural, 39(9), 2452-2459. DOI: 10.1590/S0103-84782009005000207
https://doi.org/10.1590/S0103-8478200900...
).

Table 3
Summary of individual analyzes of variance for grain yield (GY) and oil yield (OY) evaluated in 16 sunflower genotypes cultivated in 16 environments belonging to National Sunflower Trials Network.

Stratification has usually been performed for predictable environmental variations (Allard & Bradshaw, 1964Allard, R. W., & Bradshaw, A. D. (1964). Implications of genotype-environmental interactions in applied plant breeding. Crop Science, 4(5), 503-508.), usually only for site effect. The effect of the years is an unpredictable factor and therefore, there is no way to carry out the zoning. For this study it was possible to verify that half and three quarters of the environment combinations present a predominantly complex interaction for grain and oil yield, respectively (Table 5), so, environment clustering was difficult. Palmas was the only environment that presented predominantly simple interaction when compared to all others, regardless of the evaluated trait, indicating that it could be excluded from the network without this impacting on the quality of this one; in addition, the test conducted in this environment presented low values that contrasted a lot in relation to the others. In some cases, values of the complex part above 100% were found, for example, for the environment pair two and seven Planaltina 2012 and 2013 in relation to grain yield, suggesting that the average correlation of the genotypes in these environments is negative (Cruz et al., 2012Cruz, C. D., Regazzi, A. J., & Carneiro, P. C. (2012). Modelos biométricos aplicados ao melhoramento genético (4 ed.). Viçosa, MG: UFV.), in this case, non-controllable factors influenced the response in these two trials.

Optimum environment number analysis is a result of exhaustive search, so that they are presented at the end of the analysis, which environments have a greater or lesser impact on the network quality. In this study the established coefficient was 90%. The evaluation for oil yield showed that the reduction of any environment did not impact the representativeness of the network as much as the minimum correlation value obtained between the complete and the reduced network was 94.07% when the Muzambinho environment was withdrawn (Table 6).

When two environments were removed from the analysis, the estimated correlation values remained above the established cutoff point. However, the withdrawal of three environments should be judicious to characterize the grain yield, since the combination of the Canarana, Muzambinho, and Vilhena (2013) A tests, if eliminated, would reduce the correlation value to 85.24%, below the established cutoff value. However, if there was a need to exclude half of the network environments, the combination of the environments of Nova Porteirinha, Planaltina 2013, Uberlândia, Vilhena A 2012, Vilhena B 2012, Canarana, Campo Verde and Vilhena would have an interesting correlation of 96.87% with the original network. On the other hand, the withdrawal of the Planaltina, Uberlândia, Vilhena A 2012, Canarana, Jaíba, Manduri, Muzambinho and Vilhena A 2013 would result in a sudden decrease in the representativeness of the network (58.5% correlation), which would make the recommendation unfeasible.

Table 4
Summary of joint analysis of variance for grain yield (GY) and oil yield (OY) evaluated in 16 sunflower genotypes cultivated in 16 environments belonging to National Sunflower Trials Network.

Table 5
Complex part of the interaction GxE (%) between pairs of environments and sunflower genotypes for grain yield (upper diagonal) and oil yield (lower diagonal), evaluated by Cruz and Castoldi (1991Cruz, C. D., & Castoldi, F. L. (1991). Decomposição da interação genótipos x ambientes em partes simples e complexa. Ceres, 38(219), 422-430.) method. Values that represent predominantly complex interactions are highlighted in bold.

For oil yield (Table 7), the removal of the trial A of Vilhena 2012 could impact the quality of the environmental network, leading to a correlation of 86.92%, demonstrating its importance to the network. The analysis of the optimum number of environments allows the selection of the most distinct environments that would impact on the loss of the environmental variability of the network. In this case, the environments Uberlândia, Vilhena A 2012 and Muzambinho are fundamental, as the maintenance of these resulted in high values of correlation even when eliminating all others. The definition of more important environments is closely related to the geographical and climatic conditions of each one, since these particularities define the genotype responses.

An important difference in the analysis of the environments for the two traits was that, for grain yield, the removal of any environment did not reduce the correlation to values below the cut-off point. However, when evaluating the oil yield, removal of the environment represented by trial A of Vilhena 2012, for example, would lead to a drop in correlation. It is therefore important that before deciding to remove sites from an experimental network, evaluate the behavior of each important trait and which environments have been determinant for it over time. In addition, to evaluate which environmental combination will provide greater correlation with the data obtained in the complete experimental network.

Optimum environment number analysis also provides a graphical view of the impact of the environment removal from the environmental network. Once the cutoff point has been established, the different trial combinations are tested using the Pi statistics of Linn and Binns (1988Lin, C. S., & Binns, M. R. A. (1988). A superiority measure of cultivar performance for cultivar x location data. Canadian Journal of Plant Science, 68(1), 193-198. DOI: 10.4141/cjps88-018
https://doi.org/10.4141/cjps88-018...
) and plotted against the pre-established correlation value. Thus, as seen for grain yield, removal of any environment did not reduce the correlation to less than 90% (Figure 1A and B), however the removal of two or more environments could imply the loss of the network representativity. For oil yield, the withdrawal of Jaíba (environment 11) would provide the same efficiency in the genotypic discrimination, by means of the Pi statistic since it would maintain the correlation of this stability and adaptability measure, between the reduced and the complete network above the cut-off point (Figure 1C). However, the removal of Muzambinho would lead to a less efficient reduced network, since this led to a correlation between the genotypes performance, measured by Pi, below the cut-off point (Figure 1D).

Table 6
Mean, minimum and maximum correlation values according to the number of environments analyzed for grain yield.

Table 7
Mean, minimum and maximum correlation values according to the number of environments analyzed for oil yield.

Figure 1
Correlation between performance of genotypes measured by the Pi statistic of Linn and Binns (1988Lin, C. S., & Binns, M. R. A. (1988). A superiority measure of cultivar performance for cultivar x location data. Canadian Journal of Plant Science, 68(1), 193-198. DOI: 10.4141/cjps88-018
https://doi.org/10.4141/cjps88-018...
) in all environments and the performance obtained with reduced number of environment for grain yield (A and B) and oil yield (C and D).

The graphical analysis allows the breeder to visualize the impact of the environment removal from a network in a simple and fast way. Once detected points below the established correlation, the researcher could infer about the minimum number of environments of the network and suggest, through consistent information of several testing years, the environment elimination.

Conclusion

Optimal environment number analysis is a useful tool in breeding programs, since it allows to exclude redundant environments from experimental networks of the breeding programs.

The environments Palmas, Vilhena, Canarana and Muzambinho must be maintained in the National Sunflower Trials Network, so that the grain and and oil yield can be well characterized.

Acknowledgements

To the researchers and institutions that evaluated the trials of the National Sunflower Trials Network, whose experimental data were necessary for the elaboration of this work

References

  • Allard, R. W., & Bradshaw, A. D. (1964). Implications of genotype-environmental interactions in applied plant breeding. Crop Science, 4(5), 503-508.
  • Cruz, C. D. (2013). GENES - a software package for analysis in experimental statistics and quantitative genetics. Acta Scientiarum. Agronomy, 35(3), 271-276. DOI: 10.4025/actasciagron.v35i3.21251
    » https://doi.org/10.4025/actasciagron.v35i3.21251
  • Cruz, C. D., & Castoldi, F. L. (1991). Decomposição da interação genótipos x ambientes em partes simples e complexa. Ceres, 38(219), 422-430.
  • Cruz, C. D., Regazzi, A. J., & Carneiro, P. C. (2012). Modelos biométricos aplicados ao melhoramento genético (4 ed.). Viçosa, MG: UFV.
  • Grunvald, A. K., Carvalho, C. G. P., Oliveira, A. C. B., Pires, J. L. F., Carvalho, H. W. L., & Oliveira, I. R. (2014). Adaptabilidade e estabilidade de híbridos de girassol convencional e alto oleico na Região Sul do Brasil. Revista Ciência Agrária, 57(3), 217-223. DOI: 10.4322/rca.ao1270
    » https://doi.org/10.4322/rca.ao1270
  • Jocic, S., Miladinovic, D., & Kaya, Y. (2015). Breeding and genetics of sunflower. In E. Martínez-Force, N. T. Dunford, & J. J. Ans Salas (Eds.), Sunflower: chemistry, production, processing, and utilization (p. 1-27). Springfield, IL: AOCS Press.
  • Kaya, Y., Jocic, S., & Miladinovic, D. (2012). Sunflower. In S. Gupta (Ed.), Technological innovations in major world oil crops (p. 85-129). New York, NY: Springer.
  • Leite, R. M. V. B. C., & Borba Filho, A. B. (2014). Ata - XX reunião nacional de pesquisa de girassol Londrina, PR: Embrapa Soja.
  • Leite, R. M. V. B. C., Brighenti, A. M., & Castro, C. (2005). Girassol no Brasil Londrina, PR: Embrapa Soja.
  • Lin, C. S., & Binns, M. R. A. (1988). A superiority measure of cultivar performance for cultivar x location data. Canadian Journal of Plant Science, 68(1), 193-198. DOI: 10.4141/cjps88-018
    » https://doi.org/10.4141/cjps88-018
  • Nobre, D. A. C., Resende, J. C. F., Brandão Junior, D. S., Costa, C. A., & Morais, D. L. B. (2012). Desempenho agronômico de genótipos de girassol no norte de Minas Gerais. Revista Agro@mbiente On-line, 6(2), 140-147. DOI: 10.18227/1982-8470ragro.v6i2.781
    » https://doi.org/10.18227/1982-8470ragro.v6i2.781
  • Paniego, N., Heinz, R., Fernandez, P., Talia, P., Nishinakamasu, V., & Hopp, H. E. (2007). Sunflower. In C. Kole (Ed.), Oilseeds: genome mapping and molecular breeding in plants (p. 153-177). Berlin, GE: Springer.
  • Porto, W. S., Carvalho, C. G. P., Pinto, R. J. B., Oliveira, M. F., & Oliveira, A. C. B. (2008). Evaluation of sunflower cultivar for central Brazil. Scientia Agricola, 65(2), 139-144. DOI: 10.1590/S0103-90162008000200005
    » https://doi.org/10.1590/S0103-90162008000200005
  • Porto, W. S., Carvalho, C. G. P., Pinto, R. J. B., Oliveira, M. F., & Oliveira, A. C. B. (2009). Adaptabilidade e estabilidade de genótipos de girassol para a região subtropical do Brasil. Ciência Rural, 39(9), 2452-2459. DOI: 10.1590/S0103-84782009005000207
    » https://doi.org/10.1590/S0103-84782009005000207
  • Ribeiro, M. F. S., Daros, E., Caires, E. F., & Vasconcellos, M. E. C. (2011). Desempenho agronômico da cultura do girassol em diferentes condições edafoclimáticas do Sudeste paranaense. Bragantia, 70(3), 550-560. DOI: 10.1590/S0006-87052011000300010
    » https://doi.org/10.1590/S0006-87052011000300010

Publication Dates

  • Publication in this collection
    21 Oct 2019
  • Date of issue
    Jan-Dec 2020

History

  • Received
    09 May 2018
  • Accepted
    27 Sept 2018
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