RA 00110.pdf - OAR@ICRISAT
RA 00110.pdf - OAR@ICRISAT
RA 00110.pdf - OAR@ICRISAT
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ance to the pest) because of their ability to produce a<br />
large number of tillers.<br />
The synchrony of head emergence with peak activity<br />
of adults is determined by rainfall, cultivar duration,<br />
planting date, and cultural practices. For<br />
example, late varieties such as Sanio in Senegal;<br />
N K K and C N M 127 in Mali; Sadore, Torini, Haini<br />
Kirei, and their hybrids in Niger (Gahukar 1983b,<br />
Doumbia et al. 1984, I C R I S A T 1984); or the very<br />
early varieties such as Souna from Segou (SRCVO<br />
1980), are not attacked by the spike worm (pseudoresistance).<br />
There is significant correlation between<br />
infestation rate and crop duration (r=-0.83) and time<br />
of head emergence (r=-0.70 to -0.88) (ICRISAT<br />
1981; Guevremont 1982, 1983).<br />
Certain head characteristics could be related to R.<br />
aJbipunctella damage, e.g., length and position of<br />
bristles; and head length, compactness, and diameter.<br />
Of all these characteristics, only compactness —<br />
measured by the number of florets or grains—is<br />
correlated to pest damage (r=0.81) (Guevremont<br />
1983, Gahukar 1984). In the Malian Souna variety,<br />
the combination of compactness and short involucre<br />
and peduncle bristles probably make it unsuitable<br />
for oviposition and larval development (Guevremont<br />
1982).<br />
Stem-borer tolerance is found in the varieties<br />
I N M B 106, I N M B 218, and I N M B 155 from Niger<br />
(ICRISAT 1984). In Zongo, a secretion in the galleries<br />
where the larvae are lodged (NDoye 1977) may be<br />
a resistance mechanism (antibiosis).<br />
Blister beetle incidence was not related to head<br />
chracteristics (position of florets within the glumes,<br />
shape, length, direction, and rigidity of bristles) in<br />
Mali (Doumbia et al. 1984).<br />
Biological Control<br />
Risbec (1950, 1960) has listed the natural enemies<br />
(predators, parasites, pathogens) of most millet<br />
pests. Recently about 20 auxiliary parasites of<br />
Raghuva have been identified for different development<br />
stages (Table 1) (Vercambre 1978; Gahukar<br />
1981; Guevremont 1982, 1983; Bhatnagar 1983,<br />
1984). Among these, Bracon hebetor (Braconidae),<br />
Litomastix sp. (Encyrtidae), and Cardiochiles spp.<br />
(Chalcidiae) appear to be of major importance with<br />
parasitism of up to 48% for eggs, 95% for larvae, and<br />
2% for pupae (Guevremont 1983, Bhatnagar 1984).<br />
Their activity has a significant effect only at the end<br />
of the cropping season, especially in dry years.<br />
The biology of these three parasites, and their<br />
subsequent use as biological control agents has been<br />
studied.<br />
B. hebetor is a very active larval ectoparasite with<br />
a life cycle of 7-10 days. But its performance can be<br />
inhibited by hyperparasites: Eurytoma sp. (Pteromalidae)<br />
and particularly Pediobus sp. (Eulophidae)<br />
which attacks up to 56% of the parasites in Niger<br />
(Guevremont 1983). B. hebetor survives on Ephestia<br />
sp., a pest of stored grain, during the dry season.<br />
Studies are underway to determine the most effective<br />
use of B. hebetor in pest control by transferring<br />
it naturally to pearl millet fields in Aug-Sep.<br />
Litomastix sp. is a polyembryonic egg parasite<br />
that remains in dispause until February when it<br />
emerges from prepupal host larvae in the soil. Up to<br />
800 parasites have been collected from a single larva.<br />
Although parasitism can potentially reach 80-90%<br />
under favorable conditions, it has not yet exceeded<br />
31% in the field (Vercambre 1978, Bhatnagar 1984).<br />
Cardiochiles sp. parasitized only 8% of the larvae<br />
during flowering (Bhatnagar 1984), but the number<br />
of parasites is expected to increase with crop diversification.<br />
This pest develops in Jul-Aug on Heliothis<br />
armigera in association with Acarthospium hispidium,<br />
and later appears on the same insect host as it<br />
infests maize crops in Aug-Sep.<br />
Larvae and pupae of Acigona are attacked by<br />
several parasites (Table 2) (Risbec 1950, NDoye<br />
1977, Gahukar 1981), including Syzeuctus sp. (Ichneumonidae).<br />
This parasite is common in Senegal<br />
and Nigeria where it is reported to have reduced the<br />
larval population by up to 30% (Harris 1962, Bhatnagar<br />
1984). Another parasite Gonozius procerae<br />
attacks only 1-2% of the diapausing larvae (NDoye<br />
1980).<br />
Six parasites infest the larvae and pupae of the<br />
midge Geromyia penniseti: Tetyrastichus diplosidis,<br />
Platygaster sp., Aphanogmus sp., Eupelmus popa,<br />
Eupelmus sp., Tetrastichus sp. The most important<br />
is Tetrastichus sp. (Eulophidae), which represents<br />
80% of the total pest population at the end of the<br />
season (Coutin and Harris 1968).<br />
Diptera parasites (Heliocobia sp.) were collected<br />
from Mylabris holocericea adults (CILSS 1985).<br />
The parasites are less active during the dry season<br />
when their insect hosts are in diapause and climatic<br />
conditions break the parasite-pest synchrony. Although<br />
local natural enemies of certain pests contribute<br />
greatly to reducing the insect host population,<br />
they are not capable of controlling the pests.<br />
The introduction of well-selected exotic species<br />
would be more useful. These should have a good<br />
host-location ability, specificity to the host, high<br />
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