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224<br />

M.S.T. ABBAS<br />

from that of males. Abraham, Faleiro, Shuaibi, <strong>and</strong> Alabdan (2001), however,<br />

reported that R. ferrugineus captured <strong>by</strong> pheromone traps were most likely<br />

female dominated, as the sex ratio in captured weevils was 1 male:2.7 females.<br />

El-Garhy (1996) found this ratio to be 1 male:2 females (in Ismaelyia,<br />

Egypt) while Abbas et al. (2006) found that out of 18,047 RPW captured from<br />

five date palm plantations (Ras Al-Khaima, UAE) during 2000 <strong>and</strong> 2001, the<br />

females represented 60.2% of the total catch, while males represented 39.8%<br />

(almost 1 male:1.51 females). Finally, Abd-Allah <strong>and</strong> Al-Khatri (2005) compared<br />

the catch of different colours of pheromone traps hung on the palm trees at 1 m<br />

height in Sultanate of Oman. These authors found that the orange or red traps<br />

captured almost 2-fold RPW compared to the blue ones. However, sex ratio in<br />

the captured weevils was almost 1 male:1.1 females, in the 3 traps.<br />

5.3. Entomopathogenic Nematodes<br />

EPN from the families Steinernematidae <strong>and</strong> Heterorhabditidae are widely<br />

regarded as being excellent biological control agents for a number of insect pests<br />

in soil <strong>and</strong> cryptic habitats (Gaugler & Kaya, 1990; Kaya & Gaugler, 1993).<br />

They possess many positive attributes including their wide range hosts, safety to<br />

vertebrates, plants as well as non target <strong>org</strong>anisms, exemption from registration<br />

in many countries, ease of in vitro production <strong>and</strong> application using st<strong>and</strong>ard<br />

spray equipments. The two families bear mutualistic bacteria in the intestine,<br />

belonging to the genera Xenorhabdus (in Steinernematidae) <strong>and</strong> Photorhabdus<br />

(in Heterorhabditidae).<br />

The free-living, non-feeding 3rd instars (infective juveniles) of these<br />

nematodes possess attributes of both insect parasitoids or predators <strong>and</strong><br />

entomopathogens. Like parasitoids <strong>and</strong> predators, they have chemo-receptors<br />

<strong>and</strong> are motile; like pathogens, they are highly virulent, killing their host victims<br />

within 24–48 h.<br />

5.3.1. Pathogenicity to RPW<br />

Several laboratory studies were carried out to evaluate the efficiency of EPNs<br />

against larvae <strong>and</strong> adults of R. ferrugineus. Abbas <strong>and</strong> Hanounik (1999) tested<br />

the virulence of Steinernema riobravis, S. carpocapsae (All strain) <strong>and</strong><br />

Heterorhabditis sp. (Egyptian isolate) against larvae <strong>and</strong> adults of RPW. They<br />

found that the three nematode species caused 10–100% mortality in the larvae,<br />

at concentrations ranging from 30 to 240 infective juveniles (IJs) per larva. The<br />

trial was carried out in Petri-dishes lined with filter paper. The LC 50 values were<br />

51, 61 <strong>and</strong> 56.6 IJs per larva for S. riobravis, S. carpocapsae <strong>and</strong><br />

Heterorhabditis sp., respectively. Adults RPW were less susceptible to the<br />

nematode infection, as the corresponding LC 50 values for the three species were<br />

900, 1,100 <strong>and</strong> 1,416 IJs per adult. However, such infected adults produced<br />

2,000–242,000 IJs per weevil, but no correlation was found between dose <strong>and</strong><br />

IJs production.

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