ecome an <strong>in</strong>tegral part <strong>of</strong> the process <strong>of</strong> identify<strong>in</strong>g <strong>and</strong> study<strong>in</strong>g pest resistance <strong>in</strong> <strong>groundnut</strong> (Prasad et al., 2000). Groundnut <strong>genotypes</strong> such as ICGV- 86699 Tan, Mutant III, GPBD-6, GPBD-5, ICGV- 86699 Red, GPBD-4 <strong>and</strong> susceptible check (JL-24), were utilized for rear<strong>in</strong>g S. litura. The effect <strong>of</strong> these <strong>genotypes</strong> on larval, pre pupal, pupal, pre oviposition, oviposition <strong>and</strong> post oviposition period, larval weight, larval mortality, per cent pupal survival ,pupal weight ,adult longevity, per cent adult emergence <strong>and</strong> fecundity <strong>of</strong> S. litura was ascerta<strong>in</strong>ed on each <strong>of</strong> the <strong>elite</strong> <strong>genotypes</strong>. The present study demonstrated existence <strong>of</strong> substantial amount <strong>of</strong> variability <strong>in</strong> host, affect<strong>in</strong>g these biological parameters. 5.1.1.1 Larval period The length <strong>of</strong> larval duration was affected <strong>in</strong> larvae fed on foliage <strong>of</strong> test <strong>genotypes</strong> (Table 2) <strong>and</strong> there by reduces biotic potential <strong>of</strong> the pest. The <strong>genotypes</strong> Mutant III <strong>and</strong> ICGV- 86699 Tan recorded longer larval duration <strong>in</strong> each <strong>in</strong>stars compare to other <strong>genotypes</strong>. While <strong>in</strong> susceptible <strong>genotypes</strong> viz., GPBD-4 <strong>and</strong> JL-24 recorded shorter larval duration (Fig. 3). The present study corroborate with the f<strong>in</strong>d<strong>in</strong>gs <strong>of</strong> Patil et al. (1995) where <strong>in</strong> S. litura had stretched larval duration on ICGV-87165, ICGV- 86350 <strong>and</strong> ICGV- 87264. Bioassay carried out with the larvae to underst<strong>and</strong> the mechanism <strong>of</strong> resistance by Wightman <strong>and</strong> Ranga Rao (1994) revealed no antibiosis effect on II <strong>and</strong> IV <strong>in</strong>star larvae when fed to matured leaves <strong>of</strong> ICGV- 86031. Spodoptera frugiperda (S.) fed with resistant florunner took more days to develop compared to larvae fed with curly leaf (Todd et al., 1991). It has also been showed that longer larval duration on resistant <strong>genotypes</strong>, NC Ac -2243 (Xi Jia LI , 1987) was longer. 5.1.1.2 Larval weight <strong>and</strong> larval mortality The <strong>genotypes</strong> Mutant III <strong>and</strong> ICGV- 86699 Tan recorded significantly low larval weight <strong>and</strong> high percentage <strong>of</strong> mortality at all the stages compared to susceptible <strong>genotypes</strong> GPBD-4 <strong>and</strong> JL-24 (Table 3 <strong>and</strong> Fig. 2). The larval per cent mortality was high on resistant <strong>genotypes</strong> <strong>in</strong> early stages compare to susceptible <strong>genotypes</strong> <strong>in</strong>dicat<strong>in</strong>g the vulnerability <strong>of</strong> neonate larvae to the exist<strong>in</strong>g resistant factor. Accord<strong>in</strong>g to Stevenson et al. (1993) <strong>in</strong> pest control strategies, neonate larvae should be a primary target <strong>in</strong> host plant resistance because plant damage can be m<strong>in</strong>imized if pest is elim<strong>in</strong>ated as early <strong>in</strong> the life cycle as possible. The higher larval mortality <strong>of</strong> S.litura on resistant <strong>groundnut</strong> <strong>genotypes</strong> like ICGV-86031, wild tetraploid Arachis manticola was also reported by many workers (Kulkarni, 1989; Dwivedi et al., 1993; Wightman <strong>and</strong> Ranga Rao, 1994; Patil et al., 1995; Prasad <strong>and</strong> Gowda, 2006). Mortality at early stages has also been observed <strong>in</strong> Heliothis zea when reared on maize plant. The development <strong>of</strong> first stadium larvae <strong>of</strong> H. zea was retarded by the presence <strong>of</strong> chlorogenic acid <strong>and</strong> rut<strong>in</strong> <strong>in</strong> artificial diet (Isman <strong>and</strong> Duffey, 1982). Present f<strong>in</strong>d<strong>in</strong>gs corroborates with the f<strong>in</strong>d<strong>in</strong>gs <strong>of</strong> Prasad <strong>and</strong> Gowda (2006) where <strong>in</strong> the larval weight was significantly low from larvae fed on the foliage <strong>of</strong> resistant <strong>genotypes</strong> NC Ac 343, Mutant 28-2 <strong>and</strong> R 9227. S<strong>in</strong>gh <strong>and</strong> Sachan (1992) identified ICGV-86030, ICGV- 86031 <strong>and</strong> NC Ac 343 as resistant to S. litura based on survival, weight ga<strong>in</strong> <strong>and</strong> larval duration. The differential response <strong>of</strong> the <strong>genotypes</strong> on larval parameters <strong>in</strong>dicates the possibility <strong>of</strong> antibiosis mechanisms <strong>of</strong> resistance operat<strong>in</strong>g <strong>in</strong> them. The effect <strong>of</strong> resistant <strong>genotypes</strong> on larval mortality <strong>in</strong> early stage, ga<strong>in</strong> <strong>in</strong> larval weight <strong>and</strong> growth <strong>of</strong> the larvae could obviously be due to chemical factors, i.e. antibiosis as elucidated by Pa<strong>in</strong>ter (1951). The chemicals viz., querecit<strong>in</strong> glycosiden, chlorogenic acid <strong>and</strong> rut<strong>in</strong> have been reported to be the cause for resistance <strong>in</strong> wild Arachis species (Stevenson, 1993) <strong>and</strong> could be the cause for antibiosis. However, physical resistance (leaf thickness) may be also important as panitrometric studies showed that leaves <strong>of</strong> resistant wild Arachis species required a greater bit<strong>in</strong>g effort than did the leaves <strong>of</strong> susceptible TMV-2 <strong>and</strong> more susceptible <strong>of</strong> Arachis. 5.1.1.3 Pupal development <strong>and</strong> moth emergence The resistant effect <strong>of</strong> Mutant III <strong>and</strong> ICGV- 86699 Tan were also observed on pupal duration, pupal weight, per cent pupal survival <strong>and</strong> moth emergence (Table 5 <strong>and</strong> 4). Similar
Larval period <strong>and</strong> Total developmental period (egg-adult) 60 50 40 30 20 10 0 Larval period Total developmental period (egg-adult) Fecundity (eggs/female) GPBD-5 ICGV-86699 Red ICGV-86699 Tan GPBD-6 Mutant-III GPBD-4 JL-24 (Susceptible check) Genotypes Fig. 2: In vitro biology <strong>of</strong> Spodoptera litura on <strong>elite</strong> <strong>groundnut</strong> <strong>genotypes</strong> 700 600 500 400 300 200 100 0 Fecundity (eggs / female)
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SCREENING ELITE GENOTYPES AND IPM O
- Page 3 and 4: CONTENTS Sl. No. Chapter Particular
- Page 5 and 6: Figure No. LIST OF FIGURES Title 1.
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- Page 11 and 12: observed on Dwarf Mutant, the lowes
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- Page 19 and 20: 1. JL-24 (Susceptible check) 2. ICG
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- Page 23 and 24: Table 1: Performance of elite groun
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- Page 29 and 30: Table 4: Biological parameters of S
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- Page 37 and 38: Table 8: Thysanoplusia orichalcea p
- Page 39 and 40: Table 10: Spilarctia obliqua popula
- Page 41 and 42: 4.2.4.2 50 days after sowing The de
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- Page 51 and 52: Table 19: Economics of IPM modules
- Page 53: Per cent defoliation 50 45 40 35 30
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- Page 65 and 66: REFERENCES Agasimani, C. A., Ravish
- Page 67 and 68: Kennedy, F. J. S., Rajamanickam. K.
- Page 69 and 70: Prasad, M. N. R. and Gowda, M. V. C
- Page 71 and 72: Tiwari, S. N., Rathore, Y. S. and B
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