Abstract

Nineteen parental lines including five male sterile A-lines (AH002A, AH003A, AH209A, S5001A, J16A) and fourteen restorers (A1-GH, A3, S5, J6, J7N, J7J, J8, J9, J10, J11, J12, J13, J14, J17) were crossed using the North Carolina II statistical method. Studies of combining ability and heritability were conducted on selected parents along with their seventy F 1 hybrids for main ornamental traits. Plant height, crown size and length of node had obvious additive genetic effects, high (>0.50) broad sense heritability and high narrow sense heritability (length of node was medium). Pedicel length showed approximately equivalent maternal and paternal additive genetic effects, high broad sense heritability and medium (0.30–0.50) narrow sense heritability. Number of whorls of ray florets across capitulum and number of branches were able to take advantage of heterosis. The relationship between general combining ability and specific combining ability in Zinnia elegans depended on materials and traits. Male sterile two-type line was pivotal in the hybridization breeding of Z. elegans. S5001A, AH002A and A1-GH, A3, J14 which performed high negative GCA effects in PH, PL, LN and type I in PH, PL, NW, LN were ideal female and male parents of potted flowering plants; AH209A, J16A and S5, J10, J17 which displayed positive GCA effects and almost type I in PH, PL, LN were ideal female and male parents of cut flowers, respectively. For potted flowering plants, AH002A × J17, AH209A × A1-GH and S5001A × J6 with high negative SCA effects in PH, PL and LN were the most promising combinations, AH002A × S5, AH003A × A3 and J16A × J6 were the subprime combinations; for cut flowers, AH209A × S5, AH209A × J17 and J16A × J17 with high positive SCA effects in PH, PL and LN were the primary combinations, AH209A × J9 and S5001A × J10 were the secondary combinations.

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