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materials in a sick-plot (i.e. a field in which the<br />
soil contains resting spores of the DM causal<br />
fungus) is unreliable and restrictive. A new<br />
technique was required which (i) would allow<br />
even exposure to inoculation of many thousands<br />
of segregating lines, (ii) would allow flexibility in<br />
size and location of the testing site, and<br />
(iii) could be used efficiently in the postrainy<br />
season as well as in the rainy season. Evidence<br />
from two field experiments during the rainy<br />
season clearly indicated that the sporangia<br />
(ephemeral asexual spores produced in millions<br />
on infected plants each night) played a major role<br />
in the early infection of plants and buildup of the<br />
disease (development of the epidemic) in the field<br />
when high humidities prevailed. This information<br />
was used to develop a screening technique<br />
based on sporangia produced by "infector<br />
rows" (a known high-susceptible hybrid) planted<br />
in every third row 15 days before seeding of the<br />
test rows. Inoculum is provided for initiating<br />
infection in the infector rows by strategically<br />
placed pots of infected plants, and the necessary<br />
humidity is provided by fine-mist irrigation in the<br />
evening hours. The test materials are planted<br />
when the infector rows show rapid disease development<br />
(15 to 21 days after seeding of the<br />
infector rows) and the mist irrigation is continued<br />
twice weekly until the test materials reach<br />
heading stage. Throughout the screening area,<br />
after every 10 test lines, a known high-susceptible<br />
hybrid (indicator) is planted at the same time as<br />
the test lines in order to measure the success of<br />
the inoculation process. This technique was<br />
highly effective during both the rainy and postrainy<br />
seasons in 1976, and details of the screening<br />
results are presented below and in the breeding<br />
subprogram report.<br />
Screening Activities at ICRISAT Center<br />
Using the infector-row system, 4 hectares of<br />
breeding material were screened at ICRISAT<br />
Center for resistance to DM in both the rainy<br />
and postrainy seasons. This was a joint activity<br />
between the breeding and pathology staffs. In the<br />
population-improvement materials, selfing and<br />
sibbing for the next cycle of selection was carried<br />
out in the disease nursery utilizing only D M -<br />
resistant plants. A measure of the advance<br />
achieved in this process is presented in Table 22.<br />
In addition to the ICRISAT breeding materials,<br />
230 millet lines were tested in the disease<br />
nursery for scientists working in the All-India<br />
Coordinated Millet Improvement Project.<br />
Multilocational Screening<br />
The International Pearl Millet Downy Mildew<br />
Nursery (IPMDMN). One of the features of<br />
certain types of resistance is that it "breaks<br />
down" through the ability of the pathogen to<br />
overcome the resistance. In an attempt to find<br />
Table 22. Comparison of downy mildew susceptibility in four populations after one generation of selection<br />
under heavy disease pressure during rainy and postrainy seasons at ICRISAT Center, 1976.<br />
Lines with < 5 % incidence<br />
Maximum incidence<br />
Population Rainy' Postrainy Rainy Postrainy<br />
G A M 73 S 2 's<br />
G A M 73 FS<br />
G A M 75 S 1 's<br />
Late Composite<br />
(%)<br />
3.1<br />
. 9.0<br />
0.0<br />
33.3<br />
(%)<br />
50.0<br />
16.7<br />
9.5<br />
68.4<br />
(%)<br />
76.59<br />
69.35<br />
87.75<br />
59.57<br />
(%)<br />
50.0<br />
41.4<br />
69.7<br />
31.0<br />
a Resistant plants were selfed in rainy season 1976 and the progeny retested during the postrainy season.<br />
65