<abstract xmlns="http://www.w3.org/1999/xhtml"> The objective of this study was to assess genotype-by-environment interaction for seed glucosinolate content in winter rapeseed cultivars grown in western Poland using the additive main effects and multiplicative interaction model. The study concerned 25 winter rapeseed genotypes (15 F1 CMS ogura hybrids, parental lines and two European cultivars: open pollinated Californium and F1 hybrid Hercules), evaluated at five locations in a randomized complete block design with four replicates. The seed glucosinolate content of the tested genotypes ranged from 5.53 to 16.80 μmol∙g-1 of seeds, with an average of 10.26 μmol∙g-1. In the AMMI analyses, 48.67% of the seed glucosinolate content variation was explained by environment, 13.07% by differences between genotypes, and 17.56% by genotype-by-environment interaction. The hybrid PN66×PN07 is recommended for further inclusion in the breeding program due to its low average seed glucosinolate content; the restorer line PN18, CMS ogura line PN66 and hybrids PN66×PN18 and PN66×PN21 are recommended because of their stability and low seed glucosinolate content.</abstract>

The objective of this study was to assess genotype-by-environment interaction for seed glucosinolate content in winter rapeseed cultivars grown in western Poland using the additive main effects and multiplicative interaction model. The study concerned 25 winter rapeseed genotypes (15 F1 CMS ogura hybrids, parental lines and two European cultivars: open pollinated Californium and F1 hybrid Hercules), evaluated at five locations in a randomized complete block design with four replicates. The seed glucosinolate content of the tested genotypes ranged from 5.53 to 16.80 μmol∙g-1 of seeds, with an average of 10.26 μmol∙g-1. In the AMMI analyses, 48.67% of the seed glucosinolate content variation was explained by environment, 13.07% by differences between genotypes, and 17.56% by genotype-by-environment interaction. The hybrid PN66×PN07 is recommended for further inclusion in the breeding program due to its low average seed glucosinolate content; the restorer line PN18, CMS ogura line PN66 and hybrids PN66×PN18 and PN66×PN21 are recommended because of their stability and low seed glucosinolate content.

Genotype-by-environment interaction for seed glucosinolate content in winter oilseed rape (Brassica napus L.) using an additive main effects and multiplicative interaction model

Biometrical Letters

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

The objective of this study was to assess genotype-by-environment interaction for seed glucosinolate content in winter rapeseed cultivars grown in western...

Genotype-by-environment interaction for seed glucosinolate content in winter oilseed rape (Brassica napus L.) using an additive main effects and multiplicative interaction model

Data publikacji: 22 cze 2018

Zakres stron: 85 - 96

DOI: https://doi.org/10.2478/bile-2018-0007

Słowa kluczowe
Brassica napus, seed glucosinolate content, AMMI, stability

© 2018 Jan Bocianowski, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Genotype-by-environment interaction for seed glucosinolate content in winter oilseed rape (Brassica napus L.) using an additive main effects and multiplicative interaction model

Data publikacji: 22 cze 2018

Zakres stron: 85 - 96

DOI: https://doi.org/10.2478/bile-2018-0007

Słowa kluczoweBrassica napus, seed glucosinolate content, AMMI, stability

© 2018 Jan Bocianowski, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Słowa kluczowe
Brassica napus, seed glucosinolate content, AMMI, stability