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require restorer lines, it might be extremely useful for progenies were ratooned and transferred to the IRRI
breeding japonica and basmati rice hybrids. Phytotron glasshouse with 27/21 ◦ C day/night temper-
Thermosensitive genic male sterility (TGMS), de- ature, to induce seed setting. Seeds harvested from
veloped in China (Yuan, 1987), Japan (Maruyama these plants were sown in mid-November up to the
et al., 1990), and IRRI (Voc & Virmani, 1991) is first week of December to expose the desired plants
controlled by a single recessive nuclear gene which to a fertility-inducing temperature (below 30 ◦ C in
interacts with temperature to express pollen sterility or February) at the critical stage (5–15 days after panicle
fertility (Maruyama et al, 1990; Borkakati & Virmani, initiation) for seed multiplication and further selec-
1995). Seeds of a TGMS line are multiplied by selfing tion. Remaining seeds of the selected TGMS plants
when they are exposed to the right temperature during were seeded in late January to early February to ex-
their critical growth stage which in the tropics was 5– pose them at the critical stage, to a sterility-inducing
15 days after panicle initiation (Maruyama et al., 1990; temperature above 30 ◦ C in March-April for evaluat-
Borkakati & Virmani, unpublished). Commercial F1 ing pollen and/or spikelet sterility of plants in their
hybrids are produced by pollinating a TGMS line with progenies. Pollen sterility was determined by stain-
any fertile line or variety. This hybrid rice breeding ing pollen grains with 1% Iodine Potassium Iodide
system, called the two-line method (Yuan, 1987) in- (IKI) solution, while spikelet fertility was determined
creases breeding efficiency. This paper presents results by counting the filled spikelets in proportion to the
on developing TGMS lines and reports performance of total number of spikelets of randomly selected bagged
some two-line rice hybrids. panicles of a plant.
In another experiment, selected TGMS lines were
seeded in January, June, and August to expose them to
Materials and methods a sterility-inducing temperature (above 30 ◦ C) during
panicle initiation to flowering (in March-April, Aug-
At the initial phase of the TGMS breeding program, Sept. and Sept-Oct, respectively) and test their sterility
performance of the temperate japonica TGMS gene behavior. To induce fertility for their seed multiplica-
donor Norin PL 12, provided by Japan through the tion these TGMS lines were seeded in November to
IRRI-Japan Shuttle Project, was tested at IRRI farm expose them at the critical stage to a fertility-inducing
(altitude 21 m), Aritao, Nueva Vizcaya (altitude 100 temperature 28–29 ◦ C in January-February. These sus-
m) and in high altitude areas, Banaue, Ifugao (alti- pected TGMS lines were also grown in higher altitude
tude about 100 to 1040 m in the Philippines. Norin (150 m above sea level) areas – Lucban, Quezon and
PL 12 was crossed with elite indica (IR36, BG 90- Aritao, Nueva Vizcaya – to induce pollen and spikelet
2, IR46830B, IR62829B, IR9761-17-1R) and tropical fertility.
japonica (IR47686-17-1B) rice cultivars and the se- Two new indica TGMS lines, IR68945-4-33-4-
gregated materials generated were handled by the 14 and IR68945-11-5-31 developed from the program
pedigree selection procedure. To determine the right were crossed with some elite rice cultivars used as
time of planting in IRRI farm, the average temperature male parents to produce 246 experimental two-line
was computed on the basis of 15 year temperature data rice hybrids. These hybrids were evaluated along with
from the IRRI Climate Unit. 209 three-line in an unreplicated testcross nursery in
Breeding materials were grown during a period of 1993 and 1994. In the 1995 wet season 30 two-line
high temperature (maximum temperature above 30 ◦ C hybrids were evaluated in an observational yield trial
in the dry and wet seasons in the field to identify using an augmented design. Six promising hybrids
progenies showing TGMS segregants. Six hundred were further tested in preliminary yield trial with 5
plants per F2 population were grown and 30 fertile m × 2 m plot size and laid out in a randomized
plants were selected based on phenotypic acceptab- complete block design with four replications. Stand-
ility. In F3 -F5 generations, agronomically superior ard statistical analyses were conducted to calculate
families were identified and subsequently, selection least significant difference (LSD) for testing the sig-
of fertile plants was done in the families showing se- nificance of difference between two-line hybrids and
gregation for sterility. From each progeny consisting checks.
of 36 plants, seven to ten fertile plants possessing
normal spikelet fertility were selected. Phenotypically
acceptable male sterile segregants among the F5 -F6

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