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Kerala Agricultural University, Thrissur
The history of agricultural education in Kerala can be traced back to the year 1896 when a scheme was evolved in the erstwhile Travancore State to train a few young men in scientific agriculture at the Demonstration Farm, Karamana, Thiruvananthapuram, presently, the Cropping Systems Research Centre under Kerala Agricultural University. Agriculture was introduced as an optional subject in the middle school classes in the State in 1922 when an Agricultural Middle School was started at Aluva, Ernakulam District. The popularity and usefulness of this school led to the starting of similar institutions at Kottarakkara and Konni in 1928 and 1931 respectively.
Agriculture was later introduced as an optional subject for Intermediate Course in 1953. In 1955, the erstwhile Government of Travancore-Cochin started the Agricultural College and Research Institute at Vellayani, Thiruvananthapuram and the College of Veterinary and Animal Sciences at Mannuthy, Thrissur for imparting higher education in agricultural and veterinary sciences, respectively. These institutions were brought under the direct administrative control of the Department of Agriculture and the Department of Animal Husbandry, respectively. With the formation of Kerala State in 1956, these two colleges were affiliated to the University of Kerala. The post-graduate programmes leading to M.Sc. (Ag), M.V.Sc. and Ph.D. degrees were started in 1961, 1962 and 1965 respectively.
On the recommendation of the Second National Education Commission (1964-66) headed by Dr. D.S. Kothari, the then Chairman of the University Grants Commission, one Agricultural University in each State was established. The State Agricultural Universities (SAUs) were established in India as an integral part of the National Agricultural Research System to give the much needed impetus to Agriculture Education and Research in the Country. As a result the Kerala Agricultural University (KAU) was established on 24th February 1971 by virtue of the Act 33 of 1971 and started functioning on 1st February 1972. The Kerala Agricultural University is the 15th in the series of the SAUs.
In accordance with the provisions of KAU Act of 1971, the Agricultural College and Research Institute at Vellayani, and the College of Veterinary and Animal Sciences, Mannuthy, were brought under the Kerala Agricultural University. In addition, twenty one agricultural and animal husbandry research stations were also transferred to the KAU for taking up research and extension programmes on various crops, animals, birds, etc.
During 2011, Kerala Agricultural University was trifurcated into Kerala Veterinary and Animal Sciences University (KVASU), Kerala University of Fisheries and Ocean Studies (KUFOS) and Kerala Agricultural University (KAU).
Now the University has seven colleges (four Agriculture, one Agricultural Engineering, one Forestry, one Co-operation Banking & Management), six RARSs, seven KVKs, 15 Research Stations and 16 Research and Extension Units under the faculties of Agriculture, Agricultural Engineering and Forestry. In addition, one Academy on Climate Change Adaptation and one Institute of Agricultural Technology offering M.Sc. (Integrated) Climate Change Adaptation and Diploma in Agricultural Sciences respectively are also functioning in Kerala Agricultural University.
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ThesisItem Open Access Dissipation and risk assessment of select insecticides used for pest management in cabbage and cauliflower(Department of Agricultural Entomology, College of Agriculture, Vellayani, 2018) Anju Padmanabhan; KAU; Ambily PaulStudies on “Dissipation and risk assessment of select insecticides used for pest management in cabbage and cauliflower” was conducted in College of Agriculture, Vellayani, Cardamom Research Station, Pampadumpara and farmers field at Kalliyoor during 2015-2018. The present research work was under taken to study the dissipation of select insecticides viz., chlorantraniliprole 18.5 % SC, flubendiamide 39.35 % SC, indoxacarb14.5 % SC, emamectin benzoate 5 % SG, fipronil 5 % SC, quinalphos 25 % EC, cypermethrin 10% EC, acetamiprid 20% SP, thiamethoxam 25 % WG and dimethoate 30 % EC in cabbage and cauliflower, to assess their potential risks to human health, to determine their effect on soil microbial activity, to estimate the residues in cooked samples and to evaluate the efficacy of “Veggie Wash” to eliminate residues. Survey conducted among 25 each of farmers cultivating cabbage and cauliflower in plain (Thiruvananthapuram) and hill (Idukki) representing two agro climatic conditions revealed that pest infestation was more in hills when compared with plains. Accordingly, pesticide usage was higher in Idukki (84 % each) than in Thiruvananthapuram district (12 and 8 %) in cabbage and cauliflower respectively. Dissipation studies of insecticides having label claim for cabbage and cauliflower under CIB & RC in two agroclimatic regions of Kerala viz., Thiruvananthapuram and Idukki showed that the degradation of insecticides varied with crop and chemistry of the insecticides. Insecticides persisted more in cabbage under plain were flubendiamide (20 days) followed by acetamiprid and quinalphos (10 days each), while in hills, higher persistence was observed in flubendiamide, cypermethrin and quinalphos (10 days each). The lowest persistence was observed in fipronil (3 days) in cabbage under plains and acetamiprid (3 days) in hills. In cauliflower higher persistence was observed for flubendiamide, chlorantraniliprole and dimethoate in plains and flubendiamide, quinalphos (20 days each) and cypermethrin (15 days) treated plots in hills. The lowest persistence was observed for emamectin benzoate (3 days) in cauliflower under plains and hills. Risk assessment study was carried out in cabbage and cauliflower using selected insecticides under plains and hills by comparing the values of Theortical Maximum Residue Concentration (TMRC) and Maximum Permissible Intake (MPI). The result revealed that consumption of dimethoate and fipronil treated cabbage and cauliflower were found to be risky to the end users. However, all other insecticides are safe even on the same day of insecticide application. Effect of insecticides on soil microbial activity was studied in cabbage and cauliflower through the activity of urease, phosphatase and dehydrogenase enzymes. Lower reduction in urease activity was observed in flubendiamide, dimethoate and thiamethoxam treated plot and higher reduction was recorded in fipronil and quinalphos treated plots over control both in cabbage and cauliflower. However, lower reduction in phosphatase activity was recorded in flubendiamide, thiamethoxam and cypermethrin and higher reduction was observed in indoxacarb and fipronil treated plots over control. Lower reduction in dehydrogenase activity was recorded in cypermethrin, acetamiprid and thiamethoxam treated plots and higher reduction was recorded in indoxacarb and fipronil treated plots over contol in both cabbage and cauliflower. Study on extent of removal of insecticides through cooking from cabbage and cauliflower was conducted with insecticides which had more persistence revealed that 15 min cooking removed more residues and the highest removal was observed for quinalphos (54.79 %) in cabbage under plains and cypermethrin (66.47 %) in hills. However, in cauliflower the highest per cent removal was observed for chlorantraniliprole (44.78) in plains and cypermethrin (52.32 %) in hills. “Veggie wash” technology was evaluated in the cabbage and cauliflower after application of insecticides at recommended doses revealed that dipping of cabbage and cauliflower in one per cent “Veggie Wash” solution for 10 min. followed by water wash removed 12-40 per cent of treated insecticides while water wash alone removed 9 -35 per cent. The present study revealed that the dissipation pattern of insecticides varied with crop, agro climatic areas, and chemistry of the molecules. Risk assessment study shown that insecticides viz., fipronil and dimethoate posed risk on human health even at recommended dose. Studies on effect of insecticides on soil enzyme revealed that except fipronil and indoxacarb, all other insecticides under present study have less impact on soil enzymes. Decontamination studies showed that cooking at 15 min. removed 50-60 per cent of insecticides and “Veggie Wash” removed 12-40 per cent of treated insecticides. Present study urged the need to evaluate the new insecticides carefully, by considering safety to environment and human health. The risk assessment studies of all insecticides should be done before going for field level recommendations.ThesisItem Open Access Bio-ecology and management of borer pests infesting yard lond bean, Vigna unguiculata subsp. sesquipedalis (L.) verdc.(Department of Agricultural Entomology, College of Agriculture, Vellayani, 2018) Sontakke Pritin, Pramod; KAU; Amritha, V SA study on ‘Bio-ecology and management of borer pests infesting yard long bean, Vigna unguiculata subsp. sesquipedalis (L.) Verdc.’ was conducted at the College of Agriculture, Vellayani during 2014-17. The main objective was to study the biology and population dynamics of borer pest complex infesting yard long bean, Vigna unguiculata subsp. sesquipedalis (L.) Verdc. and to evolve suitable management measures. A survey was conducted in six major yard long bean growing tracts of Thiruvananthapuram district during 2015-16 to document the infestation of important borer pests and their natural enemies. The biology of major borer pests were studied under laboratory conditions and population dynamics through competitive exclusion was studied by releasing the adults of two major pod borers simultaneously on to the netted yard long bean plants. Ten varieties of yard long bean were collected and evaluated for pod borer resistance, if any as per the field screening technique of Jackai (1982). The in-vitro efficacy of microbial insecticides and field evaluation of selected new generation insecticides and their combinations were conducted in managing the borer pest complex of yard long bean. Stem fly, Ophiomyia phaseoli (Tryon), girdle beetle, Nupserha bicolour (Thoms.), blue butterfly, Lampides boeticus (L.) and spotted pod borer, Maruca vitrata (G.) were the major borer pests which infested yard long bean at their different growth stages. The infestation of O. phaseoli was recorded during seedling stage while N. bicolour infestation occurred during vegetative stage of the crop. Among the six panchayats/location, significantly highest number of girdles as well as plant infestation were recorded from Balarampuram and the maximum intensity of infestation was recorded during fourth week and it was found decreasing with increasing crop age. The occurrence of L. boeticus was recorded from all the panchayats/location with the highest pod infestation in Balarampuram panchayat, while the incidence of M. vitrata was recorded only from two panchayats (Athiyannoor and Venganoor). Correlation studies between the weather parameters and population dynamics of pests revealed that per cent pod damage by M. vitrata showed significant positive correlation with wind speed and negative correlation with rainfall, whereas, O. phaseoli showed a significant negative correlation with the sunshine hours. With regard to the biology studies, female girdle beetle was found to lay eggs (0.54 mm x 0.13 mm) inside the growing stem by making punctures and girdles for oviposition. The mean incubation period was 2.66 days. The larva is yellowish white, soft-bodied with a dark head capsule which possesses an average larval period of 31.99 days and the pupation within the stem. The life cycle was completed in 67.63±7.75 days on yard long bean. On biochemical analysis, the phenol content in the upper part of the girdle infested stem was higher than lower part. The eggs of L. boeticus were disc-shaped, finely sculptured and pale green colour with an incubation period of 3.20±0.20 days. There were four larval instars and last instar was slug like, pea green in colour. Its life cycle completes in 20-22 days. In case of M. vitrata, the mean longevity of the adult was 6.00±0.57 days. There were five larval instars which took 12.25±1.43 days to enter into pupal stage. Pupation took place in the webbed flowers/pods and the pupal period lasted for about 8.25±0.75 days. The life cycle was completed in 28.00±3.03 days. From the population dynamics studies, it was revealed that L. boeticus was dominant over M. vitrata based on the per cent pod and flower infestation. In the varietal screening of yard long bean against borer pests, the cultivar VS- 13 was found resistant against O. phaseoli with significant variation in branches infested per plant, while no significant variation was observed with respect to number of girdles per plant and percentage plant infestation in the case of N. bicolour. The cultivars VS-13 and VS-05 were found resistant against L. boeticus. The resistant cultivar, VS-13 recorded less sugar content, high phenol and maximum pod length and breadth when compared to other cultivars. Efficacy of five microbial insecticides against pod borers viz., L. boeticus and M. vitrata under laboratory conditions showed that Bt. var. kurstaki @ 1 g l-1 on 5 days after treatment (DAT) recorded the highest mortality followed by B. bassiana and M. anisopliae @ 107 spores ml-1. Foliar application of chlorantraniliprole 18.5 SC @ 30 g a.i.ha-1 was effective against O, phaseoli with the least feeding punctures per leaf (4.85) and adults per plant (0.35) followed by seed treatment with acetamiprid 20 SP @ 20 g a.i.ha-1 in field condition. Field evaluation of insecticides against L. boeticus showed that indoxacarb 14.5 SC @ 75 g a.i.ha-1 recorded lowest pod infestation (11.98 per cent) which was followed by flubendiamide 39.35 SC @ 48 g a.i.ha-1 (12.33 per cent) and thiacloprid 21.7 SC @ 120 g a.i.ha-1 (12.40 per cent). In case of percentage flower damage, chlorantraniliprole 18.5 SC @ 30 g a.i.ha-1 followed by flubendiamide 39.35 SC @ 48 g a.i.ha-1 and thiacloprid 21.7 SC @ 120 g a.i.ha-1 recorded low flower damage (5.68, 6.77 and 6.95 per cent) when compared to control (31.98 per cent). Maximum crop yield was recorded from plots treated with emamectin benzoate 5 SG @ 10 g a.i.ha-1 (160.77 g plant-1) followed by chlorantraniliprole 18.5 SC @ 30 g a.i. ha-1 (159.83 g plant-1) and flubendiamide 39.35 SC @ 48 g a.i.ha-1 (152.66 g plant-1) while in untreated plot the yield was 93.11 g plant-1. In the case of insecticide combinations against pod borer complex, seed treatment with acetamiprid 20 SP @ 20 g a.i.ha-1 and foliar application of insecticide combination (chlorantraniliprole 18.5 SC + flubendiamide 39.35 SC) at flowering stage followed by foliar application of chlorantraniliprole 18.5 SC @ seedling stage and combination (chlorantraniliprole 18.5 SC + flubendiamide 39.35 SC) at flowering stage and seed treatment with acetamiprid 20 SP @ 20 g a.i.ha-1 at seedling stage and foliar application of flubendiamide 39.35 SC @ g a.i.ha-1 were effective in reducing the flower and pod damage with less larval population and maximum crop yield. Among the borer pests of yard long bean, L. boeticus is the dominant pest based on their infestation and occurrence, whereby its incidence is more closely associated with crop stage rather than the weather parameters. From the biology studies, the vine borer, N. bicolour is found to possess maximum longevity on yard long bean than other borer pests. The resistant cultivars VS-13 and VS-54 could be utilized in future breeding programme. With regard to management of borer pests, foliar application of chlorantraniliprole 18.5 SC @ 30 g a.i.ha-1 was found effective in terms of percentage reduction in the flower and pod damage, reduced larval population and increased crop yield.ThesisItem Open Access Systematics of the tribes scymnini and stethorini (coleoptera: coccinellidae) from South India(Department of Agricultural Entomology, College of Horticulture, Vellanikkara, 2018) Vidya, C V; KAU; Haseena BhaskarFamily Coccinellidae, the lady beetles, belong to the superfamily Coccinelloidea of the order Coleoptera and comprises approximately 6000 described species worldwide. Tribes Scymnini and Stethorini of the subfamily Scymninae of Coccinellidae are economically important predators successfully used in the biological control programmes of sucking pests of crops. Members of Scymnini are mainly predators of aphids, mealybugs, whiteflies and scales, whereas Stethorini are specific to mites. Though the fauna of Scymnini and Stethorini in India is species rich, it is poorly studied. The present investigation on “Systematics of the tribes Scymnini and Stethorini (Coleoptera: Coccinellidae) from south India” was carried out during 2015-17. The objectives include the following: (1) taxonomy of the tribes Scymnini and Stethorini associated with sucking pests in different agricultural ecosystems of south India, (2) prepare a key to the species of Scymnini and Stethorini and (3) generate DNA barcode for different species of Stethorini. Purposive surveys were undertaken across different districts of Kerala, Karnataka and Tamil Nadu covering 47 locations and 64 crops under different agricultural ecosystems. Beetles and immature stages of Scymnini and Stethorini were collected along with the associated prey. Immature stages of Scymnini and Stethorini were reared to adults. The specimens were then mounted, labeled and preserved as per standard procedures. The beetles were dissected and the taxonomic characters viz., antenna, mouth parts, prosternum, tarsus, post coxal line, male and female genitalia were studied and illustrated. The specimens were identified up to species level. Descriptions, illustrations and key to genera and species of Scymnini and Stethorini of southern India were prepared. The study encompasses 28 species of Scymnini of which six are putative new species. Two species are recorded for the first time in India and two species each from south India and Kerala are new records. Scymnini include Axinoscymnus, The genera treated under Cryptolaemus, Horniolus, Nephus, Sasajiscymnus and Scymnus. The genus Scymnus, represented by 20 species, of which 18 species are placed in three subgenera viz., Scymnus, Neopullus and Pullus. Two species are treated separately, as these differ distinctly from the known subgenera. The genus Nephus is represented by three species, Axinoscymnus with two species and Cryptolaemus, Horniolus and Sasajiscymnus with one species each. Stethorini are represented by 10 species in two genera: Stethorus and Parastethorus. Two putative new species of the tribe are described. Six species of Stethorini are new reports for Kerala. Two subgenera recognized under the genus Stethorus are Stethorus and Allostethorus. represented by four species each. Stethorus keralicus, one of the most common species, has been treated separately in this study, as its characters are not in agreement with the known subgenera. The genus Parastethorus is represented by only one species. The prey ranges of Scymnini and Stethorini were documented. Species distribution map were prepared for the species studied. Twenty one species of prey in four families viz., Aphididae, Pseudococcidae, Aleyrodidae and Diaspididae were recorded in association with the tribe Scymnini. Two new prey records for Scymnini are Toxoptera odinae for Scymnus pyrocheilus and Saccharicoccus sacchari for Nephus tagiapatus. Among Scymnini, Scymnus coccivora and S. saciformis are widely distributed with wider host range of six species as prey, while species of Axinoscymnus, though widely distributed, is specific to whiteflies. Among Stethorini, Stethorus pauperculus was found to be the predominant species with wider host range, while Stethorus keralicus was specific to Raoiella indica. New prey records for Stethorini includes Tetranychus okinawanus and T. truncatus for Stethorus forficatus; T. macfarlanei for S. pauperculus and Eutetranychus orientalis for Parastethorus indira. For barcoding the species of Stethorini, DNA was isolated using Qiagen DNeasy blood and tissue kit and the COI locus was amplified and sequenced. The sequences were aligned and characteristic barcode gaps were identified for Parastethorus indira, Stethorus forficatus, S. pauperculus, S. rani, S. keralicus, S. (Allostethorus) sp. 1 and S. (Stethorus) sp.1. Pairwise distances between the sequences were analysed which showed that intraspecific divergence ranged between 0.00 to 0.03, while the interspecific distance ranged between 0.14 to 0.24. A phylogenetic tree was constructed with 21 sequences in MEGA 7 using the maximum likelihood tree method. The sequences were submitted to GenBank (NCBI) and to BOLD for the generation of species specific barcodes. The study identified 38 species of predatory coccinellids in the tribe Scymnini and Stethorini in association with aphids, mealybugs, whiteflies, scales and mites, which are serious pests of crops. Knowledge on the taxonomy of these predators and their prey range throws light on the potential of the above groups in biocontrol of sucking pests.ThesisItem Open Access Characterization of Bemisia tabaci (Gennadius) (hemiptera: aleyrodidae), for genetic variability, endosymbionts and vector-virus interactions in cassava(Department of Agricultural Entomology, College of Horticulture, Vellanikkara, 2018) Harish, E R; KAU; Mani ChellappanCassava is one of the important tuber crops cultivated all over the World. Cassava Mosaic Disease (CMD) is the most important limiting factor in its production. Silverleaf whitefly, Bemisia tabaci (Gennadius) is the vector responsible for the transmission of Cassava mosaic virus in cassava, which causes CMD. Genetic variation among the members of B. tabaci, makes them very difficult to manage. Endosymbionts present in the whitefly system could be a factor responsible for making them a successful sucking pest. There are various kinds of interactions existing between whitefly and the CMV. Studying these interactions precisely will help to understand the behavioural and physiological variations in whiteflies. In this background the present study, “Characterization of Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae), for genetic variability, endosymbionts and vector-virus interactions in cassava” was proposed and carried out at the Department of Agricultural Entomology, College of Horticulture, Vellanikkara, during Mrch 2014 to April 2016, with the objectives to analyse the genetic variability in cassava whitefly, characterization of its endosymbionts and elucidation of cassava whitefly - cassava mosaic virus interactions. Various life stages of B. tabaci were collected from different cassava growing agro ecological zones of Kerala and reared in laboratory as well as in polyhouse at optimum conditions. Genetic variability study was conducted with 10 selected ISSR primers which had shown polymorphism in their banding pattern; with amplicon size ranged between 200bp to 2900bp. Phylogenetic analysis using NTsys software revealed the presence of two major clusters with Sultan Bathery population as out group. Similarity matrix had shown up to 49 per cent variation between the samples. Polymerase chain reaction using mitochondrial cytochrome oxidase1 primers, C1-J2195 and L2-N-3014 had given amplicon of 850bp. Nucleotide sequences had shown variation up to 16.5 per cent and dendrogram generated out of the sequences using MEGA-6 (Neighbor Joining Method) gave two clusters and one out group. Sequence similarity check using reference sequences from NCBI data base indicated the presence of two biotypes, AsiaI and AsiaII5 in cassava plants of Kerala. Morphometric studies were conducted to assess the variations in different pupal and adult characters of thirteen whitefly populations. Significant variations were found in pupal length and pupal width of the biotypes. Pupal length varied between 0.746 mm to 0.668 mm and pupal width varied between 0.539 mm to 0.468 mm in female pupa. Out of 14 characters of pupa studied, variations in length and width were found to be significant. Among seven characters of adults studied, variations in wing, antennal length, body length and width were significant. AsiaI biotype was found to have lesser body length, but more width compared to AsiaII5. AsiaII5 was found to be an important biotype of B. tabaci infesting cassava in 12 out of the 13 locations surveyed. Endosymbiont characterization from whitefly using Next Generation Sequencing (NGS) - Illumina platform revealed the variations in microbiota. At phylum level, Proteobacteria was found at 87.57 per cent in whitefly populations collected from plains. The populations from high ranges contained Firmicutes at 82.67 per cent. Arsenophonus, an ‘indirect helper’ for virus spread by protecting viral coat protein from degradation in insect system with their GroEL chaperones were found at 24. 69 per cent in B. tabaci populations collected from plains. Behavioural and life cycle variation study of B. tabaci using six cassava genotypes had shown that virus infection in B. tabaci altered the dispersal and settling. Speed of movement observed to be maximum at 16.25 cm/s in non- virulent female whiteflies on the genotype CMR-9. Life cycle of virulent and non-virulent whiteflies was found to vary between 19.57 days to 30.77 days. A thorough understanding of genetic variations, endosymbiont diversity and behavioural response to virus could help the researchers in planning proper management strategies for B. tabaci. In future, information generated of such kinds could also help the researchers and policy makers to foresee and manage any possible outbreak of the pest and avoid any havoc caused by them.ThesisItem Open Access Microbial consortium for the management of insect pests of bitter gourd (Momordica charantia L.)(Department of Agricultural Entomology College of Agriculture, Vellayani, 2018) Naveeda, S; KAU; Anitha, NThe study entitled "Microbial consortium for the management of insect pests of bitter gourd" was undertaken in the Department of Agricultural Entomology at College of Agriculture, Vellayani during the period 2013 - 2018 with an objective to isolate and identify microbial pathogens of pests of bitter gourd, develop a microbial consortium, test its compatibility with new pesticide molecules and to evaluate the efficacy of the microbial consortium against major pests of bitter gourd. Important pests of bitter gourd viz. fruit fly, Bactrocera cucurbitae, pumpkin caterpillar Diaphania indica, epilachna beetle Henosepilachna septima and red pumpkin beetle Aulacophora foveicollis were monitored from bitter gourd fields in Thiruvananthapuram and Kollam districts. One entomopathogenic fungi from diseased epilachna grub and pumpkin caterpillar larvae and one phylloplane bacteria were isolated. Kotch's postulates were proved for both the fungi. Upon preliminary screening for pathogenicity to various pests of bitter gourd, the fungi showed infectivity only towards epilachna grubs and pumpkin caterpillar whereas, the bacteria was found to be infective to epilachna grub, pumpkin caterpillar and adults of red pumpkin beetle. The fungus from both the insects was identified as Fusarium verticilloides and the bacteria was identified as Serratia marcescens Pathogenicity studies were conducted using isolates of Metarhizium anisopliae (Ma4) Beauveria bassiana (Bb5) and Lecanicillium lecanii obtained from NBAIR, Paecilomyces lilacinus isolate (rrCC 6064), Beauveria bassiana isolate (rrCC 6063) and the indigenous isolates. The fungi M anisopliae and B. Bassiana were infective to all the test insects selected whereas the P. lilacinus was found infective only to pumpkin caterpillar and fruit flies. Lecanicillium lecanii was not infective to any of the test insects. M anisopliae was more virulent to the test insects compared to B. bassiana and reported a mortality of 93.54%, 82.5%, 45%, 5%, 25%, 61.05% respectively in B. cucurbitae adults, D. indica larvae, grubs and adults of H septima, adults of A. foveicollis and nymphs of L. australis seven days after treatment at a dose of 10 8 spores Lethargic movement followed by cessation of feeding was common symptom of mycosis in all the species. Bioassay was conducted against the adults of B. cucurbitae, H septima and A. foveicollis and the larvae of D. indica and H septima using M anisopliae (Ma4), B. bassiana (Bb5) and P. lilacinus (nCC 6064). The LC 50 values for M anisopliae were 1.55x10, 0.18X10, 1.56X10 and 4.70x10 spores mL- 1 respectively for adults of B. cucurbitae, D. indica larvae, grubs and adults of H septima, adults of A. foveicollis at seven days after treatment. With respect to B. bassiana, LC 50 values were 1.65x10, 1.20x10, 1.05X10, 5.48x10 and 2.94 x 10 spores ml respectiveiy was required for the adults of B. cucurbitae, D. indica larvae, grubs and adults of H septima, adults of A. foveicollis respectively. In vitro compatibility studies were conducted between the different entomopathogenic fungi viz. B. bassiana, M anisopliae, P. lilacinus and L. Iecanii. In dual cultures, colony growth of B. bassiana and M. anisopliae got locked at the point of contact after two weeks of inoculation leaving a space of 3 to 5 mm apart from each other. In dual culture combinations of B. bassiana with P. lilacinus and L. Iecanii and M anisopliae with P. lilacinus and L. Iecanii, the colony growth stopped at two weeks after inoculation and a space of 1.5 cm to 2 cm was observed between different fungi. The interactions between various microbes in-vitro is not necessarily an indicator of their in-vivo interactions. Hence in vivo studies were conducted to assess the effect different microbial combinations viz. M anisopliae with B. Bassiana (consortium 1), M anisopliae with P. lilacinus (Consortium 2) and B. bassiana with P. lilacinus (Consortium 3) on test insects. Laboratory evaluation of the fungal consortium showed that the mixtures of various fungi were more pathogenic to the test insects in comparison with the fungi using individually. The fungal consortium 1 (Ma4 +Bb5) was highly virulent to all the test insects and resulted in per cent mortality of 100, 100, 88.33, 36.67, 36.67 and 100 respectively for adults of B. cucurbitae, D. indica larvae, grubs and adults of H septima, adults of A. foveicollis and nymphs of L. Australis seven days after treatment. Talc based formulations of the consortium maintained the required standards of colony forming units in the formulation and retained bioefficacy against various test insects. Cfu at three months after storage was 0.83 x 10 7 and 7.23 x 10 7cfu g-1 respectively for room temperature and refrigeration. The components of the consortium I, B. bassiana and M anisopliae were tested for the compatibility with five insecticides commonly used for pest management in bitter gourd in order to evaluate the suitability of integrating the product with pesticides in pest management programmes. Compatibility of both the fungi was observed for the insecticide Chlorantraniliprole 18.5 SC 0.006 % . Field experiment was conducted in bitter gourd, variety Preethi to evaluate the talc based formulation of consortium I along with insecticide Chlorantraniliprole 18.5 SC and Malathion as check. The treatments were two application of Consortium I @ 35 g L -1, consortium followed by Chlorantraniliprole 18.5 SC 0.006 %, Chlorantraniliprole 18.5 SC 0.006 % followed by Consortium I @ 35 g L-1, two applications of Chlorantraniliprole 18.5 SC 0.006 % and two applications of Malathion and untreated check. Results showed that the treatment, consortium 1 followed by Chlorantraniliprole 18.5 SC 0.006 % effectively managed populations of D. indica (0.08 larvae /10 leaves) , H septima (0.11 grubs/ 10 leaves) and A. foveicollis (1.5 adults/ plant) at five days after treatment. The percentage infestation of fruits by B. cucurbitae also got reduced from 52.18 % during pre-treatment count to 9.13% after treatment and produced the highest yield of 14.53 t ha-1. To conclude, the fungal isolate which caused natural epizootic in epilachna grub and pumpkin caterpillar larvae was identified as F. verticilloides. A bacterium S. marcescens was obtained from the phylloplane of bitter gourd and found to be pathogenic to larvae of D. indica and grubs of H septima. The fungi B. bassiana and M anisopliae were pathogenic to all the test insects. The combination of both resulted in a higher mortality of the test insects and increased the speed of kill than when treated alone. However, in dual culture studies, the fungi were incompatible. Talc based formulation of the consortium maintained the required standards of cfu in the formulations and efficacy upto three months after storage. Highest mortality of the test insects were noticed at the dose 40 g L -1 of the formulation. In the field study, consortium 1 (Ma4 + Bb5) followed by Chlorantraniliprole 18.5 SC 0.006 % was effective in managing the insect population and resulted in a high yield.