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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 />

201

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