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By D S Brar; B Hardy

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30*) when all F1s were used in the analysis (Table 1). 81 PR1A Bo A 913 A Zhangyu PR28127 PR2A SN62a IR58025 A E2-208 SN45b O-71 Toyosake E2-50 1xS-24 1xS-30 Fig. 2. Dendrogram of 15 parental lines used to develop 3-line hybrids based on 45 SSR marker variants. Table 1. Correlation between parental genetic distance and heterosis for eight traits in 48 three-line F 1 hybrid combinations (average data of 1998 wet and dry seasons). Male parent PSBRc28 Table 2. Correlation between marker heterozygosity (general) and heterosis for seven traits in 13 two-line hybrid combinations.

81 PR1A Bo A 913 A Zhangyu PR28127 PR2A SN62a IR58025 A E2-208 SN45b O-71 Toyosake E2-50 1xS-24 1xS-30 Fig. 2. Dendrogram of 15 parental lines used to develop 3-line hybrids based on 45 SSR marker variants. Table 1. Correlation between parental genetic distance and heterosis for eight traits in 48 three-line F 1 hybrid combinations (average data of 1998 wet and dry seasons). Male parent PSBRc28 Table 2. Correlation between marker heterozygosity (general) and heterosis for seven traits in 13 two-line hybrid combinations.

Naina Mohammed, and R. M. Vijayakumar, Directorate of Rice Research, Hyderabad 500 030, India. 18 Advances in rice genetics Genetic analysis of temperature-sensitive genic male sterility in rice A. E. Naina Mohammed, R. M. Vijayakumar Crosses were made between two TGMS lines, ID24 × SM5 and IC10 × JPs4. The F1s had completely normal pollen and spikelet fertility under high temperature (35 °C day/26 °C night). The F2s showed a 9 fertile:7 sterile ratio, indicating that the character is governed by two separate genes.

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