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Genetic progress of 18 years of a soybean breeding program for the Brazilian Central-West1 1 Part of the dissertation of the first author, presented to the graduate program in Bioenergy and Grains of the Instituto Federal Goiano

Progresso genético de 18 anos de um programa de melhoramento de soja para Centro-Oeste brasileiro

ABSTRACT

In a breeding program, the estimation of genetic progress over the years provides a broad view of the program as well as grounds for optimal decision-making. In this respect, the present study proposes to estimate the genetic progress of 54 soybean cultivars released to the Brazilian Midwest between the years 2000 and 2017. Two experiments were conducted during the 2017/18 crop year. Grain yield (GY), maturity group (MG), 100-seed weight (100SW), number of pods per plant (NPP), number of seeds per pod (NSP) and plant height (PH) were evaluated. Genetic progress was estimated by the direct methodology and by linear regression. According to the direct method, the average annual genetic progress was positive for GY (1.92%), 100SW (2.69%), NPP (2.31%), NSP (1.10%) and PH (0.32%), but negative for MG (-0.44%). The results obtained using both methodologies agree on the obtained increases for GY and 100SW and the decreases for MG.

Keywords:
Genetic gain; Glycine max ; production components

RESUMO

Em um programa de melhoramento genético, a estimativa do progresso genético ao longo dos anos fornece uma visão ampla do programa, bem como bases para uma ótima tomada de decisão. Nesse sentido, o presente estudo se propõe a estimar o progresso genético de 54 cultivares de soja lançadas para o Centro-Oeste brasileiro entre os anos de 2000 e 2017. Dois experimentos foram conduzidos na safra 2017/18. Foram avaliados o rendimento de grãos (RG), grupo de maturidade (GM), peso de 100 sementes (P100), número de vagens por planta (NVP), número de sementes por vagem (NSP) e altura de planta (AP). O progresso genético foi estimado pela metodologia direta e por regressão linear. De acordo com o método direto, o progresso genético anual médio foi positivo para GR (1,92%), P100 (2,69%), NVP (2,31%), NSP (1,10%) e AP (0,32%), mas negativo para GM (- 0,44%). Os resultados obtidos por ambas as metodologias concordam com os aumentos obtidos para RG e P100 e decréscimos para GM.

Palavras-chave:
Ganho genético; Glycine max ; componentes de produção

INTRODUCTION

Soybean (Glycine max (L.) Merrill) is an autogamous species originating in Asia. At present, Brazil stands out as the world’s first largest producer of soybean, with growing yields obtained in recent years (SCHWALBERT et al., 2020SCHWALBERT, R. A. et al. Satellite-based soybean yield forecast: integrating machine learning and weather data for improving crop yield prediction in southern Brazil. Agricultural and Forest Meteorology, v. 284, n. 1, p. 1-9, 2020.; SILVA JUNIOR et al., 2018SILVA JUNIOR, C. A. et al. Soybean varieties discrimination using non-imaging hyperspectral sensor. Infrared Physics & Technology, v. 89, n. 1, p. 338-350, 2018., 2020SILVA JUNIOR, C. A. et al. Mapping soybean planting area in midwest Brazil with remotely sensed images and phenology-based algorithm using the Google Earth Engine platform. Computers and Electronics in Agriculture, v. 169, n. 1, p. 1-10, 2020.). In the 2020-21 harvest, Brazil produced 133 million tons of soybean from a planted area of 38 million hectares, representing an average yield of 3,517 kg ha-1 (COMPANHIA NACIONAL DE ABASTECIMENTO, 2021COMPANHIA NACIONAL DE ABASTECIMENTO (BRASIL). Boletim de monitoramento agrícola. v. 9, n. 12, 2021.). Of this total, the Center-West was the most representative region (52 million tons), with the largest cultivated area (16.1 million hectares) (COMPANHIA NACIONAL DE ABASTECIMENTO, 2021COMPANHIA NACIONAL DE ABASTECIMENTO (BRASIL). Boletim de monitoramento agrícola. v. 9, n. 12, 2021.).

Given the notoriety of soybean in Brazil, breeding companies have invested in the development of new cultivars with traits desired by the market (LIU et al., 2017LIU, X. et al. Genetic variation of world soybean maturity date and geographic distribution of maturity groups. Breeding Science, v. 67, n. 3, p. 221-232, 2017.; LU et al., 2015LU, S. et al. QTL mapping for flowering time in different latitude in soybean. Euphytica, v. 206, n. 3, p. 725-736, 2015.; TODESCHINI et al., 2019TODESCHINI, M. H. et al. Soybean genetic progress in South Brazil: physiological, phenological and agronomic traits. Euphytica, v. 215, n. 7, p. 124, 2019.), such as high yield; shorter cycle; adaptability to mechanization; resistance to lodging, diseases, pests and nematodes; among others. However, determining the effectiveness of a breeding program over the years requires estimating the genetic progress achieved. This estimate can provide a broad view of the program as well as grounds for decision-making regarding any change in selection methods (FALCONER; MACKAY, 1996FALCONER, D. S.; MACKAY, T. F. C. Introduction to quantitative genetics. 3. ed. London: Longman Scientific and Technical, 1996. 464 p.).

Studies have demonstrated genetic gains in grain yield (GY), in the soybean crop (RINCKER et al., 2014RINCKER, K. et al. Genetic improvement of US soybean in maturity groups II, III, and IV. Crop Science, v. 54, n. 4, p. 1419-1432, 2014.; TOLEDO et al., 1990TOLEDO, J. F. de et al. Genetic gain in soybean in Paraná state, Brazil, obtained by breeding. Pesquisa Agropecuária Brasileira, v. 25, n. 1, p. 89-94, 1990.). These gains may be due to several factors, e.g. increased number of seeds per plant and per pod (RINCKER et al., 2014RINCKER, K. et al. Genetic improvement of US soybean in maturity groups II, III, and IV. Crop Science, v. 54, n. 4, p. 1419-1432, 2014.), greater resistance to lodging (MORRISON; VOLDENG; COBER, 2000MORRISON, M. J.; VOLDENG, H. D.; COBER, E. R. Agronomic changes from 58 years of genetic improvement of short season soybean cultivars in Canada. Agronomy Journal, v. 92, n. 4, p. 780-784, 2000.), shorter vegetative period (FELIPE; GERDE; ROTUNDO, 2016FELIPE, M. de; GERDE, J. A.; ROTUNDO, J. L. Soybean genetic gain in maturity groups III to V in Argentina from 1980 to 2015. Crop Science, v. 56, n. 6, p. 1-12, 2016.), higher photosynthetic rate (LIU et al., 2012LIU, G. et al. Development of yield and some photosynthetic characteristics during 82 years of genetic improvement of soybean genotypes in northeast China. Australian Journal of Crop Science, v. 6, n. 10, p. 1416-1422, 2012.) and increased nutrient absorption efficiency (MCFARLENE; O’CONNOR, 2014MCFARLANE, I.; O’CONNOR, E. A. World soybean trade: Growth and sustainability. Modern Economy, v. 5, n. 5, p. 580-588, 2014.).

Several methodologies have been developed to estimate genetic progress, such as the direct method; Vencovsky method, Fernandes, Morais and Abbud method and Breseghello method; the regression method with original data; the method employing control treatment as a correction factor; the regression method with standardized data; and the method of Fonseca Júnior. The advantage of the direct method lies in that it allows the evaluation of genotypes released in different years, in different environments, during the same crop year. In the linear regression method, the genetic gain is obtained directly by estimating the slope of the equation of the line (TODESCHINI et al., 2019TODESCHINI, M. H. et al. Soybean genetic progress in South Brazil: physiological, phenological and agronomic traits. Euphytica, v. 215, n. 7, p. 124, 2019.). On the other hand, it requires viable seeds from old cultivars for multiplication in sufficient quantity for the execution of the experiment (ATROCH; NUNES, 2000ATROCH, A. L.; NUNES, G. H. de S. Genetic progress in lowland rice in the State of Amapá, Brazil. Pesquisa Agropecuária Brasileira, v. 35, n. 4, p. 767-771, 2000.).

In view of the above-described scenario, the present study was developed to estimate genetic progress-using the direct and regression methods-for production components, phenotypic traits and yield in cultivars released to the Brazilian Midwest between the years 2000 and 2017 by a soybean breeding program for the Center-West region of Brazil.

MATERIAL AND METHODS

The experiments were carried out during the 2017/18 crop year at the Coodetec research station (17º45’57” S, 51º01’44” W, average altitude 844 m) and at Instituto Federal Goiano, Rio Verde Campus (17º48’26” S, 50º54’08” W, average altitude 739 m). Both sites are located in the municipality of Rio Verde, state of Goiás, Brazil. Rio Verde is situated in soybean macro-region 3 and micro-region 301, according to the third approach to agricultural zoning, proposed by Santos et al. (2018)SANTOS, H. G. dos et al. Sistema brasileiro de classificação de solos. 5. ed. Brasilia: Embrapa, 2018. 356 p..

This study examined 54 soybean cultivars released by a breeding program to the Brazilian Midwest between 2000 and 2017 (number of cultivars released each year: 2000 - one; 2003 - two; 2005 - one; 2007 - three; 2008 - one; 2009 - nine; 2010 - three; 2011 - eight; 2012 - four; 2013 - nine; 2014 - six; 2015 - two; 2016 - two; and 2017 - three). In the months from July to October 2017, all cultivars were multiplied to standardize vigor and germination for the establishment of the experiments. Sowing took place on 10/17/2017 and 11/02/2017, respectively, at the research station of Coodetec and at IF Goiano.

The experiment was laid out in a randomized block design with three replicates. Plots consisted of four 4-m rows spaced 0.50 m apart, with a final plant stand of 300,000 plants. The two central rows were considered the usable area for the evaluations. All cultivation treatments were carried out in accordance with Embrapa (2013)EMBRAPA. Tecnologias de produção de soja: Região Central do Brasil 2014. Londrina: Embrapa Soja, 2013. 265 p..

The following traits were evaluated: grain yield (GY), obtained by weighing the grains of each plot, adjusting the result for 13% moisture and extrapolating it to kg.ha-1; maturity group (MG), estimated as proposed by Zdziarski et al. (2018)ZDZIARSKI, A. D. et al. Key soybean maturity groups to increase grain yield in Brazil. Crop Science, v. 57, n. 3, p. 1155-1165, 2018.; 100-seed weight (100SW), obtained by averaging a random take of 100 grains three times in each plot and weighing on a digital scale; number of pods per plant (NPP), determined by counting the number of pods from six plants sampled randomly within each plot and averaging; number of seeds per pod (NSP), obtained by dividing the total number of seeds by the total number of pods; and plant height (PH, in cm), determined by measuring the main stem of six random plants within each plot at the physiological maturity stage.

Data were subjected to individual analysis of variance (Equation 1). After checking for homogeneity of the residual mean squares for all the experiments involved in the analysis by the method of the ratio of the largest and smallest least squares of the residue (REGAZZI et al., 1999REGAZZI, A. J. et al. Análise de experimentos em látice quadrado com ênfase em componentes de variância. Pesquisa Agropecuária Brasileira, v. 34, n. 11, p. 1987-1997, 1999.), a joint analysis was carried out for all the traits under study (Equation 2).

(1) γ i j = μ + G i + B j + ε i j

(2) γ i j k = μ + G i + A j + G A i j + ε i j k

Individual Analysis of Variance

Where: γij is the observed value of genotype i in block j; μ is the overall average of the character; Gi is the effect of genotype i; Bj is the effect of block i; and εij is the random error associated with genotype i in block j.

Joint Analysis of Variance

Where: γijk is the observed value of genotype i in environment j in block k; μ is the overall average of the character; Gi is the effect of genotype i; Aj is the effect of environment j; and εijk is the experimental error associated with plot ijk.

To estimate the combined genetic progress, the mean of each genotype in both environments and of the cultivars released each year, for each trait, was obtained and the direct method was applied. The method consists of estimating the y¯iy¯i difference, termed “total difference”, observed in a given year i', relative to the previous year i. For the purpose of estimating genetic progress, year i is the year of registration of the cultivar.

Genetic difference ΔG is defined as follows: ΔGii=(y¯i’y¯i).

Therefore, ΔGi’i can be taken as an estimator of changes in the mean occurring between years i and i', which is attributed to genotypic changes or an increase in the average productive potential of the treatments.

These estimates (ΔGii,ΔGii,,ΔGn,n1) can be obtained for each biennium. The sum of these quantities represents the cumulative genetic progress; average increase per year is the ratio of cumulative progress to the number of years of evaluation; and relative progress can be estimated as the ratio of estimated progress to the average of the initial cycle.

To estimate genetic progress, simple linear regression analysis was performed between the release years (independent variable) and the means of the agronomic variables (GY, 100SW, NPP, NSP, PH and MG) per year. To check for possible associations, Pearson’s correlation analysis was carried out and the t test was applied. The analysis of variance was performed using the Genes software (CRUZ, 2016CRUZ, C. D. Genes Software-extended and integrated with the R, Matlab and Selegen. Acta Scientiarum. Agronomy, v. 38, n. 4, p. 547-552, 2016.) and the regression analyzes using the basic package of the R software.

RESULTS AND DISCUSSION

The sources of variation of genotype and genotype × environment interaction (G×E) were significant by the F test for all evaluated traits (p < 0.05). To estimate genetic progress, the means of the environments were used. Coefficients of variation (CV%) ranged between 8.54 and 19.47%, for PH and NSP, respectively, indicating good experimental precision (data not shown).

There was an increase in GY over the 18 years of breeding, considering the annual genetic progress (ΔG) of 1.92% obtained for this trait, which corresponds to 20.80 kg ha-1 per year (Table 1). A similar result is illustrated in Figure 1A, which shows that the coefficient of the regression line was 27.61 kg ha-1 per year and significant at 5% by the t test (p < 0.05). Similar results were obtained by Koester et al. (2014)KOESTER, R. P. et al. Historical gains in soybean (Glycine max Merr.) seed yield are driven by linear increases in light interception, energy conversion, and partitioning efficiencies. Journal of Experimental Botany, v. 65, n. 12, p. 3311-3321, 2014. (26.45 kg ha-1 per year, in the USA) and by Todeschini et al. (2019)TODESCHINI, M. H. et al. Soybean genetic progress in South Brazil: physiological, phenological and agronomic traits. Euphytica, v. 215, n. 7, p. 124, 2019. (40.06 kg ha-1 per year, in the south of Brazil). Toledo et al. (1990)TOLEDO, J. F. de et al. Genetic gain in soybean in Paraná state, Brazil, obtained by breeding. Pesquisa Agropecuária Brasileira, v. 25, n. 1, p. 89-94, 1990. evaluated the efficiency of the soybean breeding program in the state of Paraná between 1981 and 1986 and observed gains of 1.8% and 1.3% for the early- and semi-early-maturing genotypes, respectively.

Table 1
Genetic progress (∆G) for grain yield (GY) (kg ha-1) and maturity group (MG) over 18 years of the soybean breeding program

Figure 1
Simple linear regression between release year and grain yield

It should be noted that the GY of the cultivar released in 2000 (the only cultivar of that year and the oldest in the data history) exceeded 4600 kg ha-1, indicating high yielding potential. This cultivar obtained similar GY means to those produced by the cultivars released in the years 2008, 2014 and 2017. For this reason, cumulative genetic progress may have been limited, mainly, by linear regression analysis.

The GY means for the cultivars released in 2015 and 2016 (Table 1) were lower than those of the cultivars released in the previous years. This was due to the introgression of wild cultivars in the breeding program, which was aimed at increasing tolerance to nematodes, a trait desired by the market that may have restricted genetic progress for GY.

Maturity group decreased on average by 0.44 per year (Table 1), and, by the regression line, by -0.270 per year, which was significant at 1% by the t test (p < 0.01) (Figure 1B). These are expected results, given that in the Brazilian Center-West conditions, where a second harvest is performed (February to May), soybean cultivars with a shorter cycle are desirable for the market. A reduction in the cycle of cultivars over the years of breeding was also observed by Liu et al. (2012)LIU, G. et al. Development of yield and some photosynthetic characteristics during 82 years of genetic improvement of soybean genotypes in northeast China. Australian Journal of Crop Science, v. 6, n. 10, p. 1416-1422, 2012. and Wu et al. (2015)W U, T. et al. Characterizing changes from a century of genetic improvement of soybean cultivars in Northeast China. Crop Science, v. 55, n. 5, p. 2056-2067, 2015.. Todeschini et al. (2019)TODESCHINI, M. H. et al. Soybean genetic progress in South Brazil: physiological, phenological and agronomic traits. Euphytica, v. 215, n. 7, p. 124, 2019. evaluated the genetic progress of agronomic and physiological traits in 29 soybean cultivars available for cultivation in the southern region of Brazil between the years 1965 and 2011 and observed an average decrease in total plant cycle of 0.29 days per year.

Hundred-seed weight (100SW), number of pods per plant (NPP) and number of seeds per plant (NSP) are among the main components of grain production in soybean. Genetic progress for 100SW was 0.16 g, which represents 2.69% per year; for NPP, 0.11 and 2.31% per year (Table 2); and, for NSP, -0.45 and 1.10% per year (Table 3). A different result was obtained by the slope of the regression line, which showed a gain of 0.102 g in 100SW (p < 0.05) per year and a decrease of 0.609 (ns) and 1.449 (p < 0.05) for NPP and NSP, respectively (Figure 1C, D and E). It is important to note that the different adopted methods and the means of the cultivars released in 2005 for NPP and NSP (108.31 and 190.86, respectively) may have influenced the regression coefficients.

Table 2
Genetic progress (∆G) for 100-seed weight (100SW) and number of pods per plant (NPP) over 18 years of the soybean breeding program
Table 3
Genetic progress (∆G) for number of seeds per pod (NSP) and plant height (PH) over 18 years of the soybean breeding program

Divergent results are commonly found for these traits. Todeschini et al. (2019)TODESCHINI, M. H. et al. Soybean genetic progress in South Brazil: physiological, phenological and agronomic traits. Euphytica, v. 215, n. 7, p. 124, 2019. evaluated genetic progress in soybean by linear regression and reported positive gains for NPP and non-significant gains for 100SW and NSP. These authors concluded that gains in productivity are associated with NPP, similarly to the results reported by Kahlon and Board (2012)KAHLON, C. S.; BOARD, J. E. Growth dynamic factors explaining yield improvement in new versus old soybean cultivars. Journal of Crop Improvement, v. 26, n. 2, p. 282-299, 2012. and Suhre et al. (2014)SUHRE, J. J. et al. Soybean yield partitioning changes revealed by genetic gain and seeding rate interactions. Agronomy Journal, v. 106, n. 5, p. 1631-1642, 2014.. However, Wang et al. (2016)WANG, C. et al. Seventy-five years of improvement of yield and agronomic traits of soybean cultivars released in the Yellow-Huai-Hai river valley. Crop Science, v. 56, n. 5, p. 2354- 2364, 2016. investigated genetic progress through regression in 25 soybean cultivars released from 1929 to 2004 in China and described that modern cultivars have lower NPP and NSP and higher 100SW, which is associated with higher grain yield, corroborating the results found by Cui and Yu (2005)CUI, S. Y.; YU, D. Y. Estimates of relative contribution of biomass, harvest index and yield components to soybean yield improvements in China. Plant Breeding, v. 124, n. 5, p. 473-476, 2005. and Wu et al. (2015)W U, T. et al. Characterizing changes from a century of genetic improvement of soybean cultivars in Northeast China. Crop Science, v. 55, n. 5, p. 2056-2067, 2015..

Genetic progress for PH was -0.59 cm and 0.32% per year (Table 3), with the regression showing a slope of -0.22 and no significance detected by the t test (Figure 1F). Decreasing PH was observed in other studies of genetic progress in soybean (RAMTEKE et al., 2011RAMTEKE, R. et al. Genetic progress of soybean varieties released during 1969 to 2008 in India. Indian Journal of Genetics and Plant Breeding, v. 71, n. 4, p. 333-340, 2011.; ROGERS et al., 2015ROGERS, J. et al. Agronomic performance and genetic progress of selected historical soybean varieties in the southern USA. Plant Breeding, v. 134, n. 1, p. 85-93, 2015.; TODESCHINI et al., 2019TODESCHINI, M. H. et al. Soybean genetic progress in South Brazil: physiological, phenological and agronomic traits. Euphytica, v. 215, n. 7, p. 124, 2019.). Decreases in PH may be directly related to greater resistance to lodging (TODESCHINI et al., 2019TODESCHINI, M. H. et al. Soybean genetic progress in South Brazil: physiological, phenological and agronomic traits. Euphytica, v. 215, n. 7, p. 124, 2019.). According to Silva et al. (2017)SILVA, F. et al. Soybean breeding. Viçosa, MG: UFV, 2017. 563 p., tall plants (above 100 cm) generally do not show great resistance to lodging, which can cause grain losses during mechanized harvesting.

Grain yield was positively and significantly correlated with 100SW (p < 0.01) and negatively with MG (p < 0.05). These results indicate that, in this soybean breeding program, genetic progress in GY is associated with an increase in 100SW (as shown in Figure 2C, D and E), corroborating the findings of Wang et al. (2016)WANG, C. et al. Seventy-five years of improvement of yield and agronomic traits of soybean cultivars released in the Yellow-Huai-Hai river valley. Crop Science, v. 56, n. 5, p. 2354- 2364, 2016..

Figure 2
Simple linear correlation between all variables

Among the productivity traits, there was an estimated negative correlation for 100SW with NPP (p < 0.05), MG (p < 0.01) and NSP (p < 0.05) and a positive correlation between NPP and NSP (p < 0.001). Maturity group was negatively and significantly correlated with GY (p < 0.05) and MHS (p < 0.005) and positively with NPP (p < 0.05) and NSP (p < 0.05). According to Resende (2015)RESENDE, M. D. V. de. Genética quantitativa e de populações. Viçosa, MG: Suprema, 2015. 463 p., indirect selection can be practiced based on correlation estimates to obtain genetic gains for a main trait. Breeding strategies that prioritize indirect selection of the highest means for 100SW and the lowest means for MG can increase genetic progress in the next cultivars released.

CONCLUSION

The breeding program has been efficient to obtain the most productive cultivars and with the least maturity group. The direct and regression methods showed positive genetic gain for grain yield and 100-seed weight and negative for maturity group. In this soybean breeding program, genetic progress in grain yield is associated with an increase in 100-seed weight.

ACKNOWLEDGEMENTS

The authors thank Fundação de Amparo à Pesquisa do Estado de Goiás, FAPEG and Instituto Federal Goiano for the financial support.

REFERENCES

  • ATROCH, A. L.; NUNES, G. H. de S. Genetic progress in lowland rice in the State of Amapá, Brazil. Pesquisa Agropecuária Brasileira, v. 35, n. 4, p. 767-771, 2000.
  • COMPANHIA NACIONAL DE ABASTECIMENTO (BRASIL). Boletim de monitoramento agrícola. v. 9, n. 12, 2021.
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  • FELIPE, M. de; GERDE, J. A.; ROTUNDO, J. L. Soybean genetic gain in maturity groups III to V in Argentina from 1980 to 2015. Crop Science, v. 56, n. 6, p. 1-12, 2016.
  • KAHLON, C. S.; BOARD, J. E. Growth dynamic factors explaining yield improvement in new versus old soybean cultivars. Journal of Crop Improvement, v. 26, n. 2, p. 282-299, 2012.
  • KOESTER, R. P. et al. Historical gains in soybean (Glycine max Merr.) seed yield are driven by linear increases in light interception, energy conversion, and partitioning efficiencies. Journal of Experimental Botany, v. 65, n. 12, p. 3311-3321, 2014.
  • LIU, G. et al. Development of yield and some photosynthetic characteristics during 82 years of genetic improvement of soybean genotypes in northeast China. Australian Journal of Crop Science, v. 6, n. 10, p. 1416-1422, 2012.
  • LIU, X. et al. Genetic variation of world soybean maturity date and geographic distribution of maturity groups. Breeding Science, v. 67, n. 3, p. 221-232, 2017.
  • LU, S. et al. QTL mapping for flowering time in different latitude in soybean. Euphytica, v. 206, n. 3, p. 725-736, 2015.
  • MCFARLANE, I.; O’CONNOR, E. A. World soybean trade: Growth and sustainability. Modern Economy, v. 5, n. 5, p. 580-588, 2014.
  • MORRISON, M. J.; VOLDENG, H. D.; COBER, E. R. Agronomic changes from 58 years of genetic improvement of short season soybean cultivars in Canada. Agronomy Journal, v. 92, n. 4, p. 780-784, 2000.
  • RAMTEKE, R. et al. Genetic progress of soybean varieties released during 1969 to 2008 in India. Indian Journal of Genetics and Plant Breeding, v. 71, n. 4, p. 333-340, 2011.
  • REGAZZI, A. J. et al. Análise de experimentos em látice quadrado com ênfase em componentes de variância. Pesquisa Agropecuária Brasileira, v. 34, n. 11, p. 1987-1997, 1999.
  • RESENDE, M. D. V. de. Genética quantitativa e de populações. Viçosa, MG: Suprema, 2015. 463 p.
  • RINCKER, K. et al. Genetic improvement of US soybean in maturity groups II, III, and IV. Crop Science, v. 54, n. 4, p. 1419-1432, 2014.
  • ROGERS, J. et al. Agronomic performance and genetic progress of selected historical soybean varieties in the southern USA. Plant Breeding, v. 134, n. 1, p. 85-93, 2015.
  • SANTOS, H. G. dos et al. Sistema brasileiro de classificação de solos. 5. ed. Brasilia: Embrapa, 2018. 356 p.
  • SCHWALBERT, R. A. et al. Satellite-based soybean yield forecast: integrating machine learning and weather data for improving crop yield prediction in southern Brazil. Agricultural and Forest Meteorology, v. 284, n. 1, p. 1-9, 2020.
  • SILVA JUNIOR, C. A. et al. Mapping soybean planting area in midwest Brazil with remotely sensed images and phenology-based algorithm using the Google Earth Engine platform. Computers and Electronics in Agriculture, v. 169, n. 1, p. 1-10, 2020.
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  • TODESCHINI, M. H. et al. Soybean genetic progress in South Brazil: physiological, phenological and agronomic traits. Euphytica, v. 215, n. 7, p. 124, 2019.
  • TOLEDO, J. F. de et al. Genetic gain in soybean in Paraná state, Brazil, obtained by breeding. Pesquisa Agropecuária Brasileira, v. 25, n. 1, p. 89-94, 1990.
  • WANG, C. et al. Seventy-five years of improvement of yield and agronomic traits of soybean cultivars released in the Yellow-Huai-Hai river valley. Crop Science, v. 56, n. 5, p. 2354- 2364, 2016.
  • W U, T. et al. Characterizing changes from a century of genetic improvement of soybean cultivars in Northeast China. Crop Science, v. 55, n. 5, p. 2056-2067, 2015.
  • ZDZIARSKI, A. D. et al. Key soybean maturity groups to increase grain yield in Brazil. Crop Science, v. 57, n. 3, p. 1155-1165, 2018.

Edited by

Editor-in-Chief: Prof. Alek Sandro Dutra - alekdutra@ufc.br

Publication Dates

  • Publication in this collection
    24 Mar 2023
  • Date of issue
    2023

History

  • Received
    18 Jan 2021
  • Accepted
    03 Oct 2022
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