STUDY OF YIELD POTENTIAL OF MAIZE SIMPLE HYBRIDS IN CYCLIC CROSS SYSTEM

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STUDY OF YIELD POTENTIAL OF MAIZE SIMPLE HYBRIDS IN CYCLIC CROSS SYSTEM Andreea ONA 1, I. HAȘ 1,2, Voichița HAȘ 2, Rodica POP 1 1 University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, Faculty of Agriculture, Department of Plant Breeding 3-5 Mănăștur Street, postcode 40037, Cluj-Napoca, Romania andreea_ona@yahoo.com 2 Agricultural Research and Development Station Turda Abstract: Maize has an important role in the Romanian agriculture, as a result of its multiple uses and optimal conditions from our country. According to the National Institute of Statistics, in the year 2011, the area cultivated with maize in Romania was of 2.613.500 hectares, with a total production of 11.666.400 tonnes of grains, placing our country on the 1st place in the European Union for the area cultivated with maize and the 2nd place for production, after France, due to an inferior yield. Otherwise, the maize yield achieved by Romania is smaller than the one achieved by the other Member States, with only 4464 kg/ha grains beside the average from the European Union of 6902 kg/ha. Yield potential can be considered genetically, the most complex characteristic. We can appreciate that the heredity of this trait is the expression of the entire genetic system of the plant, which directly or indirectly controls all fundamental involved processes (metabolic, growth and development). This paper presents the obtained results of the maize experiments fields conducted at Agricultural Research and Development Station Turda, using simple hybrids in cyclic cross system, between 2011-2012. The objectives of this paper are to highlight the genic effects involved in the heredity of the production capacity at the hybrids derived from crossings of inbred lines resulted by inbreeding, from commercial hybrids, with inbred testers, from Lancaster heterotic group. The analysis of variance for grain yield indicates significant differences between the tested maize hybrids. Comparing the general combining ability of the tested lines, reveals significant differences, the tester inbred lines being from the Lancaster germplasm group and the tested inbred lines from other heterotic groups. Also, were highlighted the effects of the specific combining ability. The effects values for the general combining ability (GCA) of the testers ranged from -85 kg/ha to +143 kg/ha. At the tested inbred lines, the value ranged between -508 kg/ha and +1141 kg/ha. The effects for the specific combining ability (SCA) was between -669 kg/ha and +589 kg/ha. Between inbred lines used as testers, production differences are not statistically significant. Among the tested inbred lines, the highest achieved average production in crosses with three testers, conducted to TA 452. The average yield was 9550 kg/ha and the additive effects for this line production capacity were, for this experimental system, of 1141 kg/ha. Regarding to the inbred lines obtained from Raissa hybrid, the highest production capacity from this experimental system was transmitted by TE 317. Our results highlight that in the production potential heredity are involved, mainly, the additive genic effects, but the non-additive genic effects are also important. Keywords: yield potential, general combining ability, specific combining ability. INTRODUCTION Maize breeding for production capacity was a constant concern of breeders (HALLAUER and MIRANDA, 1981; TROYER, 2001; SARCA TR., 2004). The study of inbred lines crossbreeding in cyclic crossing systems and diallel crossing systems have provided answers on general combining ability and on specific combining ability (CĂBULEA, 2004). Grouping the inbred lines by specific combining ability provides to breeders information on heterotic groups where those can be fit. This grouping of inbred lines helps then, in the hybrids creation process, to achieve more easily, performance hybrid combinations, 145

saving of important research funds by making logical crossings, pottentially heterotic (HAȘ, 1992, 2004; Haș et al. 1994). The objectives of this paper are to highlight the genic effects involved in the heredity of the production capacity at the hybrids derived from crossings of inbred lines inbreeding resulting, from commercial hybrids, with inbred testers, from Lancaster heterotic group. MATERIAL AND METHODS In the experimental years 2011 and 2012 were studied in compared culture with 24 variants, simple hybrids derived from crosses between inbred lines obtained from commercial hybrids (by inbreeding), as maternal forms, and testers inbred lines, from Lancaster Sure Crop germplasm group, as paternal forms. Test crosses were made in 2010, at the Agricultural Research and Development Station Turda, and the hybrids experimentation were performed, as we described above, in 2011-2012, in comparative culture, where the 21 experimental hybrids (seven hybrids made with each tester line), were studied compared with three control hybrids (Turda 201, Turda Favorit and PR39 D81). Tester and tested inbred lines are presented in Table 1. All the inbred lines used in crosses were created at ARDS Turda, Maize Breeding Laboratory (HAS VOICHITA et al., 2011). Testers inbred lines are belonging to Lancaster germplasm group, TD 268 being created by the crossing of TC 208 and C 103 (both of lines belonging to Lancaster Sure Crop group), and TC 385A and TC 399 from B Composite (in the composition of this composite, the lines C 103 and Mo 17 had a 50% share). Four of the tested inbred lines were obtained from commercial hybrid Raissa of Pioneer, and the other three (TA 452, TE 330A and TE 335) from other commercial hybrids. After the phenotypic appearance, all seven tested inbred lines seemed to have relatedness with inbred lines of SSS germplasm groups (HAS VOICHITA et al., 2011). Tabel 1 Maize inbred lines used to crosses in cyclic system Inbred Line Created at The origin of line (Pedigree no.) Tester inbred lines 1. TD 268 ARDS Turda Sel. from TC208xC103 / 5370-2-2-4-2-2. TC 385A ARDS Turda Sel. from Comp B (C103, Mo17, T248, TC208, W633) / H60-1-1-1 3. TC 399 ARDS Turda Sel. from Comp B (C103, Mo17, T248, TC208, W633) / H84-6-7-2 Tested inbred lines 1. TE 229 ARDS Turda Sel. from Raissa / 6597-3-6-2. TE 202B ARDS Turda Sel. from Raissa / 6600-1-1-1- 3. TA 452 ARDS Turda Sel. from commercial hybrid / 9390-5-1-2 4. TE 330A ARDS Turda Sel. from commercial hybrid / 9626-3-1 5. TD 364 ARDS Turda Sel. from Raissa / 8340-1-1-3- 6. TE 317 ARDS Turda Sel. from Raissa / 8345-1-5-1- 7. TE 335 ARDS Turda Sel. from commercial hybrid / 9509-1-5-3-1- Analysis of variance was performed according to the classical model, the experimental years and the 24 hybrids were considered factors in a two-factor system. Genotypes variance was decomposed non-orthogonal, after the model that Haș et al. (2010) have described, into the variance due to simple hybrids and the variance due to control hybrids. The variance of the simple hybrids was decomposed in the variance due the testers (T), the variance due the tested inbred lines (L) and the variance due the tester x tested inbred line interaction (TxL). Genic effects were calculated according to the 2 nd North Carolina model (COMSTOCK and ROBINSON, 1952), improved by CĂBULEA (2004). 146

model: Grain yield of each hybrid from experimental system is described by the following where: SH mxn yield = μ + ĝ m + ĝ n + ŝ mxn μ = the average of experienced simple hybrids; ĝ m = general combining ability due parent m (the additive effects because of parent m ); ĝ n = general combining ability due parent n (the additive effects because of parent n ); ŝ mxn = specific combining ability due to m x n interbreeding (non-additive effects due to m x n interbreeding). RESULTS AND DISCUSSIONS The analysis of variance and the non-orthogonal decomposition of genotypes variance are presented in Table 2. For simple hybrids are shown the 2 nd degree orthogonal decompositions, that highlight statistically highly significant differences between tested inbred lines, and differences at the interaction tester x tested inbred line. Analysis of variance for production capacity at the hybrids from the cyclic cross system Variability cause SP GL s² Total 562871791,00 239 Repetitions 4489627,00 4 Columns 2219918,00 4 Sample F according to: Variance of interaction Error genotypes x years Years 437102649,00 1 437102649,00 1920,97** 497,98** Genotypes 57003468,00 23 2478412,00 10,89** 2,82 Simple hybrids (SH) 52604517,49 (20) 2630225,87 11,56** 3,00** Testers (T) 1296188,11 ((2)) 648094,06 2,85 0,74 Lines (L) 40480320,60 ((6)) 6746720,10 29,65** 7,69** TxL Interactions 10828008,78 ((12)) 902334,06 3,97** 1,03 Control hybrids (CH) 23664,33 (2) 11832,17 0,05 0,01 SH-CH Comparisons 4375286,17 (1) 4375286,17 19,23** 4,98** Years x Genotypes 20188379,00 23 877755,60 3,86 Error 41867751,00 184 227542,10 Tabel 2 The productive capacity of tested simple hybrids, the effects of general combining ability and the effects of specific combining ability are presented in tabel 3. 147

Tabel 3 Productive capacity, general combining ability effects (ĝ m,n ) and specific combining ability effects (ŝ mxn ) at the cyclic cross between maize inbred lines Tested inbred line Tester inbred line TD 268 TC 385A TC 399 148 Average production of inbred line (n) Line G.C.A.(ĝ n) kg/ha ŝ mxn kg/ha ŝ mxn kg/ha ŝ mxn ŝ mxn ĝ n TE 229 7954-84 8037-229 8379 313 8124-286 TE 202B 8151 279 8142 42 7579-321 7957-452 TA 452 9548 83 9705 12 9398-95 9550*** 1141 TE 330A 7148-669 8633 589 7924 80 7902-508 TD 364 8543 237 8639 106 7990-344 8391-19 TE 317 8771-60 9087 27 8892 33 8917 507 TE 335 8156 214 7622-548 8304 334 8027-382 Average production of tester (m) 8324 8552 8352 8410 Tester G.C.A. (ĝ m) -85 143-57 DL P = 5% 543 P = 1% 716 P = 0,1% 923 Between inbred lines used as testers, production differences are not statistically significant; this situation is normal, given the relatedness degree between those inbred lines. Among the tested inbred lines, the highest achieved average production in crosses with three testers, conducted to TA 452. The average yield was 9550 kg/ha and the additive effects for this line production capacity were, for this experimental system, of 1141 kg/ha. Have exceeded the average of experimental system, the interbreedings of the line TE 317, but the additive effects of 507 kg/ha was not statistically significant. With high values for non-additive effects, with positive or negative values, were noted the following hybrid combinations: TE 330A x TC 385A, ŝ mxn = + 589 kg/ha; TE 330A x TD 268, ŝ mxn = - 669 kg/ha. The simple hybrids with the highest production owe those values due the effects: HS TA452xTC385A = 9705 kg/ha = μ(8410 kg/ha)+ĝ m (143 kg/ha)+ĝ n (1141 kg/ha)+ŝ mxn (12 kg/ha); HS TA452x D268 = 9548 kg/ha = μ(8410 kg/ha)+ĝ m (-85 kg/ha)+ĝ n (1141 kg/ha)+ŝ mxn (83 kg/ha); HS TA452xTC399 = 9398 kg/ha = μ(8410 kg/ha)+ĝ m (-57 kg/ha)+ĝ n (1141 kg/ha)+ŝ mxn (-95 kg/ha). Concerning to simple hybrids that achieved the lowest yield of experimental system, the production values were influenced by the following types of genic effects: HS TE330AxTD268 = 7148 kg/ha = μ(8410 kg/ha)+ĝ m (-85 kg/ha)+ĝ n (-508 kg/ha)+ŝ mxn (-669 kg/ha); HS TE202BxTC399 = 7579 kg/ha = μ(8410 kg/ha)+ĝ m (-57 kg/ha)+ĝ n (-452 kg/ha)+ŝ mxn (-321 kg/ha). The review of additive and non-additive genic effects involved in achieving production capacity at the most productive hybrids emphasizes the additive effects role in this process; at hybrids with the lowest yield, the additive and non-additive effects, seems that played a balanced role. We can say that only TA 452 inbred line can be firmly classified in a different heterotic group in terms of hybrid reaction than Lancaster Sure Crop. On the other studied inbred lines, obtained from valuable commercial hybrids, probably one of the parental forms belonged to the group where the tester inbred lines are in, or other non SSS group (HAȘ, 2004).

Regarding to the inbred lines obtained from Raissa hybrid, the highest production capacity from this experimental system was transmitted by TE 317; our results show that this hybrid combination is possible being retained from a SSS x Lancaster Sure Crop heterotic cross, only that the initial corn cob of segregated population that began the process of creating these lines, was closer to SSS germplasm. CONCLUSIONS 1. The 2 nd type North Carolina cyclic cross system illustrates the general combining ability of tested inbred lines, even if the tester inbred lines are genetically related. 2. From the commercial hybrids can be obtained valuable inbred lines, but it is desirable to carry out tests in order to classify them in heterotic groups in the first generations of inbreeding. 3. In the production capacity heredity are involved, mainly, the additive genic effects, but the non-additive genic effects are also important. 4. Among the tested inbred lines, the highest combining ability was recorded on TA 452, followed by TE 317. BIBLIOGRAPHY 1. CĂBULEA, I., 2004, Genetica porumbului, În: Butnaru Gallia, I. Căbulea, M. Cristea, I. Haş, Voichiţa Haş, Dana Malschi, Felicia Mureşan, Elena Nagy, T. Perju, T. Sarca, Vasilichia Sarca, D. Scurtu, Porumbul - studiu monografic, Ed. Academiei Române, Bucureşti 2. COMSTOCK, R.E., H.F. ROBINSON, 1952, Estimation of average dominance of the genes in Heterosis Edit. J. W. Gowen, p. 495 535 3. HALLAUER, A.R., J.B. MIRANDA FILHO, 1981, Quantitative genetics in maize breeding. Iowa State University Press. Ames. 4. HAȘ, I., 1992, Cercetări privind rolul formelor parentale diferențiate genetic în realizarea heterozisului la porumb, Teză de doctorat, Universitatea de Științe Agricole și Medicină Veterinară, Cluj-Napoca 5. HAȘ, I., 2004, Heterozisul la porumb, În: Butnaru Gallia, I. Căbulea, M. Cristea, I. Haş, Voichiţa Haş, Dana Malschi, Felicia Mureşan, Elena Nagy, T. Perju, T. Sarca, Vasilichia Sarca, D. Scurtu, Porumbul - studiu monografic, Ed. Academiei Române, Bucureşti 6. HAȘ, I., I. CĂBULEA, VOICHIȚA HAȘ, 1994 (a), Rolul efectelor epistatice în prognozarea formulelor de hibridare la porumb. Contribuţii ale cercetării ştiinţifice la dezvoltarea agriculturii, Redacţia revistelor agricole, vol. 5, p. 327 337 7. HAȘ, I., VOICHIȚA HAȘ, E. MUREȘAN, S. IFRIM, 2010, Folosirea descompunerilor ortogonale și neortogonale în compararea unor grupe de genotipuri, Analele INCDA Fundulea, vol. 78, (2) p. 5-16 8. HAȘ, VOICHIȚA, I. HAȘ, CAMELIA CHICINAȘ, TEODORA ȘCHIOP, I.D. COSTE, N. TRITEAN, 2011, Valoarea fenotipică și genetică a unor linii consangvinizate isonucleare de porumb, Analele INCDA Fundulea LXXIX, p. 49-66 9. SARCA, T., 2004, Ameliorarea porumbului, În: Butnaru Gallia, I. Căbulea, M. Cristea, I. Haş, Voichiţa Haş, Dana Malschi, Felicia Mureşan, Elena Nagy, T. Perju, T. Sarca, Vasilichia Sarca, D. Scurtu, Porumbul - studiu monografic, Ed. Academiei Române, Bucureşti 10. SARCA, VASILCHIA, 2004, Producerea semințelor la porumb, În: Butnaru Gallia, I. Căbulea, M. Cristea, I. Haş, Voichiţa Haş, Dana Malschi, Felicia Mureşan, Elena Nagy, T. Perju, T. Sarca, Vasilichia Sarca, D. Scurtu, Porumbul - studiu monografic, Ed. Academiei Române, Bucureşti 149

11. THE NATIONAL INSTITUTE OF STATISTICS, 2012, Crop production for the main crops, Press Release, No. 70/2012 12. TROYER, A.F., 2001, Temperate corn background, behavior and breeding. C.R.C. Press Boca Raton, London, New York, Washington, D.C. 150