Abstract:bstract-Heliothis armigera (Hubner) completed five generations in the laboratory, as well as in the field, in a year. The first generation was completed from the first week of December to the fourth week of February, the second generation from the second week of February to first week of April. The third generation from third week of August passing through the extreme summer, the fourth generation during monsoon period and the fifth last generation from the third week of September to the fourth week of Novembe… Show more
“…Laboratory experiments on Sudanese H.armigera have also shown that when, some 80 days after pupation, diapausing insects are subjected to a temperature rise from 22°C to 34"C, 8% of the pupae remain in diapause for a further 2 months and only resume development when the temperature is lowered again (Hackett & Gatehouse, 1982). Similar results have been obtained for north Indian H.armigera (Tripathi & Singh, 1993). In both cases it was proposed that this enabled insects both to survive the hot dry season and to synchronize emergence with the beginning of the rains.…”
Abstract.
A diapause induction and duration experiment was conducted in the laboratory on Indian Helicoverpa armigera (Hübner) (Lepidoptera: Noctuidae) where 79% of individuals had extended pupal periods. At 22°C and 26°C respectively, 57% and 100% of the pupae had emerged 145 days after pupation.
A mathematical model was developed to investigate the interactions between diapause, migration and pyrethroid resistance frequency development in both eastern Australia and Andhra Pradesh, India.
The effect of diapause was different in the Australian and Indian cases, providing a mechanism to conserve resistance and susceptibility respectively.
For Australia, the model simulated discriminating dose data reasonably well and showed that resistance frequencies could rise prior to the pyrethroid window without invoking cross‐resistance to non‐pyrethroid insecticides applied to cotton.
The saw‐toothed seasonal cycle of resistance development could be simulated in the Indian case without hypothesizing the existence of susceptible migrants.
The implications of‘refugia’populations for H.armigera insecticide resistance management programmes are discussed.
“…Laboratory experiments on Sudanese H.armigera have also shown that when, some 80 days after pupation, diapausing insects are subjected to a temperature rise from 22°C to 34"C, 8% of the pupae remain in diapause for a further 2 months and only resume development when the temperature is lowered again (Hackett & Gatehouse, 1982). Similar results have been obtained for north Indian H.armigera (Tripathi & Singh, 1993). In both cases it was proposed that this enabled insects both to survive the hot dry season and to synchronize emergence with the beginning of the rains.…”
Abstract.
A diapause induction and duration experiment was conducted in the laboratory on Indian Helicoverpa armigera (Hübner) (Lepidoptera: Noctuidae) where 79% of individuals had extended pupal periods. At 22°C and 26°C respectively, 57% and 100% of the pupae had emerged 145 days after pupation.
A mathematical model was developed to investigate the interactions between diapause, migration and pyrethroid resistance frequency development in both eastern Australia and Andhra Pradesh, India.
The effect of diapause was different in the Australian and Indian cases, providing a mechanism to conserve resistance and susceptibility respectively.
For Australia, the model simulated discriminating dose data reasonably well and showed that resistance frequencies could rise prior to the pyrethroid window without invoking cross‐resistance to non‐pyrethroid insecticides applied to cotton.
The saw‐toothed seasonal cycle of resistance development could be simulated in the Indian case without hypothesizing the existence of susceptible migrants.
The implications of‘refugia’populations for H.armigera insecticide resistance management programmes are discussed.
“…Its population peaks generally correspond to the full bloom and pod formation stage of the crop in the post rainy season. Temperature, relative humidity Lal 1988, Yadava et al, 1991), rainfall (Tripathi and Sharma 1985), predators (Thakur et al, 1995, Gunathilagaraj 1996 and parasitoids (Bhatnagar 1980, Srinivas and Jayaraj 1989, Thakur et al, 1995 affect the incidence and population densities of H. armigera on chickpea. Information on pest incidence under field conditions across sowing dates can be used to assess the effect of different climatic variables on pest incidence and grain yield.…”
Section: Issn: 2319-7706 Volume 8 Number 09 (2019)mentioning
“…The H. armigera larvae found active throughout the chickpea crop (Singh and Ali, 2006). The ecological parameters viz., temperature o C), photoperiod (10-14 hrs), relative humidity (15-95%) coupled with optimal and intermittent rainfall were found to influence the population buildup, adult emergence and maximum fecundity of the female moths of H. armigera (Tripathi and Singh, 1993). The pest could be managed naturaly under field conditions by larval parasitoid Campoletis chlorideae Uchida (Hymenoptera: Ichneumonidae) in chickpea ecosystem, causes up to 78% parasitisation of early instars under natural conditions (Agnihotri et al, 2011).…”
Biology and relative parasitization of larval endoparasitoid Campoletis cholrideae Uchida on Heliocoverpa armigera Hübner under sole and chickpea-coriander intercropping system (Article chronicle: Received: 04-06-2016; Revised: 12-06-2016; Accepted: 18-06-2016) ABSTRACT: The Campoletis cholrideae Uchida is a single most prominent parasitoid in chickpea for major pest Heliocverpa armigera Hubner under natural ecosystem. The purpose of present study was to investigate how weather parameters and cropping system influence on the biology, per cent parasitization in sole and intercropping system under laboratory and field conditions. In sole crop, mean parasitism by C. chlorideae on the larvae of H. armigera during 2013 and 2014 was 60.61 %, 44.66 %, respectively. Egg-larval and cocoon formation to adult emergence periods 10.16± 0.215, 4.25±2.02 days, respectively and female and male parasitoid could survive with a mean longevity of 4.50 ± 2.012 and 3.25 ± 1.85 days, respectively. Higher parasitism of 76.67% occurred on 8th collection of 11th S.W March and 60.67% on 1st collection of 11th S.W of March for respective years. The progeny of sex-ratio varied in two seasons, the mean sex ratio (M:F) were 1:1.62; 1:1.07 respective years in sole crop. In intercropping ecosystem, the overall mean parasitism by C. chlorideae on larvae of H. armigera during 2013 and 2014 with 76.96 % , 66.67 % respectively. Higher parasitism was observed (90 %) on 6 th collection of 11 th S.W March and 80 % on 1 st collection of 11 th S.W of March for respective years. However, there was steep escalation in female sex ratio in chickpea-coriander cropping system when compared with sole crop. The overall mean sex ratio were (M:F) is 1:1.90; 0.98:1.0 respective years in chickpea-coriander intercropping. A correlation with abiotic factors revealed a non-significant positive correlation with maximum temperature, evening relative humidity (RH), rain fall and sunshine hours. There was a negative correlation between parasitism and minimum temperature and morning RH in respective years under sole crop. In case of intercropping system, the result elucidated that a significant positive correlation exist with evening RH and rainfall (r= 0.951 * ; r= 0.900 * and r= 0.926 * ; r= 0.931 * ) in respective years. These results suggested that different parameters, especially cropping system and temparture, were very important for the parasitism of C. chlorideae on H. armigera.
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