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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 Biotic agents for the management of American serpentine leaf miner, Liriomyza trifolii(Burgess) (Diptera:Agromyzidae)(Department of agricultural entomology, College of horticulture, Vellanikkara, 2014) Jyothi Sara, Jacob; KAU; Maicykutty P, MathewA study on “Biotic agents for the management of American serpentine leaf miner, Liriomyza trifolii (Burgess) (Diptera: Agromyzidae)” was carried out at the Department of Agricultural Entomology, College of Horticulture, K.A.U., Vellanikkara during 2011-2013 with the objectives of collection and identification of indigenous natural enemies and to assess the pathogenicity of the entomopathogens to explore the feasibility of utilizing them for its management. Surveys were conducted in the vegetable fields for the collection and identification of natural enemies associated with L. trifolii in three districts, namely, Thrissur, Ernakulam and Kottayam from January to March, 2011. The surveys revealed the occurrence of nine species of hymenopteran parasitoids. The per cent parasitism varied from 10.96 to 58.99 per cent among the crops surveyed. Three species of eulophids, namely, Cirrospilus acadius Narendran, C. brevicorpus Shafee & Rizvi and Aprostocetus sp. as well as the braconid, Toxares sp. are new reports for India. Among the parasitoids, Closterocerus spp. were the dominant group followed by Chrysonotomyia sp. All parasitoids were solitary, larval endoparasitoids except Toxares sp. which was larval-pupal in nature. One species each of small ants (Formicidae) and a dipteran fly (Dolichopodidae) were observed as predators on L. trifolii. In the study, no entomopathogens were observed from L. trifolii. Considering the level of pesticide consumption in vegetable crops that undermine the potential of insect parasitoids and also that no entomopathogens could be observed during the survey, it was decided to evaluate entomopathogenic nematodes (EPNs) as biocontrol agents against L. trifolii. Isolation of EPNs from 72 soil samples from Thrissur, Ernakulam and Kottayam districts yielded four isolates of Steinernema carpocapsae. Bioefficacy studies carried out on these four isolates along with Steinernema bicornutum and Heterorhabditis indica showed that S. carpocapsae Isolate - 1 had the lowest LC 50 , LC 90 and LT values indicating their higher effectiveness against the maggots of the pest. 50 Pot culture study conducted to compare the potential of S. carpocapsae Isolate - 1 with other treatments showed that azadirachtin 1 EC at 0.005% was the most effective causing 84.51 per cent mortality to the maggots of L. trifolii. This was followed by the foliar application of H. indica at 32 infective juveniles (IJs)/ maggot which caused 18.98 per cent mortality. Application of Beauveria bassiana at 1×10 7 spores/ ml was not effective. In the field evaluation, fipronil 5 SC at 0.002% was found to be the most effective treatment for controlling L. trifolii followed by azadirachtin 1 EC at 0.005%. Compatibility of the IJs of the S. carpocapsae Isolate - 1, S. bicornutum and H. indica was studied with ten commonly used insecticides in the laboratory by direct exposure method. Chlorantraniliprole 18.5 SC at 0.005% was found to be the most compatible insecticide with S. carpocapsae isolate - 1 causing only 0.17 per cent mortality to IJs at 72 hours after treatment (HAT). Quinalphos 25 EC at 0.05% and chlorpyriphos20 EC at 0.05% were highly incompatible, causing 96.17 and 92.87 per cent mortality of the nematodes. Dimethoate 30 EC at 0.04% was the most compatible insecticide with S. bicornutum and caused only 0.60 per cent mortality at 72 HAT and was followed by azadirachtin 1 EC at 0.005% with 0.78 per cent mortality to the IJs. Quinalphos 25 EC at 0.05% caused 99.93 per cent mortality at 72 HAT. Heterorhabditis indica was compatible with all insecticides except quinalphos 25 EC at 0.05% which was moderately toxic resulting in 39.6 per cent mortality. The virulence, pathogenicity and multiplication of the survived IJs were not affected by the insecticide treatments. Parasitoids and EPNs were observed as potential candidates for the management of L. trifolii. Hence future studies on the bio-ecology and mass production of dominant parasitoids and standardization of methods to improve the efficacy of EPNs are suggested for the successful control of L. trifolii in polyhouses as well as in the field.ThesisItem Open Access Bioactivity of carotenoids from shrimp shell waste(Department of Processing Technology,College of Fisheries,Panangad, 2010) Sindhu, S; KAU; Sherief, P MShrimp processing waste is the single largest industrial waste in the country causing diverse environmental problems. A study was carried out to assess the extractability of astaxanthin from shrimp waste in different organic solvents and vegetable oils. Extraction was tried using wet and dried waste, with and without deproteinisation. Waste was subjected to deproteinisation using alkali and enzyme (pancreatin). The different solvent systems tried were ether:acetone:water (15:75:10 v/v/v), acetone, hexane:isopropanol (3:2 v/v) and 90% acetone v/v. Astaxanthin in the extract was quantified by measuring the OD at 470 nm in hexane. Extraction was also done using vegetable oils viz. coconut oil, soybean oil and sunflower oil. Quantification of astaxanthin in pigmented oil was done by measuring the absorbance at 485 nm using 2155 as extinction coefficient. Astaxanthin yields from deproteinised samples were significantly lower than those from non deproteinised samples. The highest astaxanthin yield of 87.14 ± 4.55μg/g was obtained with non deproteinised wet waste extracted using acetone. The astaxanthin yield was significantly lower when oil was used as the extraction medium. Of the three oils coconut oil gave the highest yield. The results showed that acetone is the best solvent for extracting astaxanthin from shrimp shell waste in wet condition. The astaxanthin content in Aristeus alcocki shell waste is double that of Pandalus borealis shell waste, which is currently used as the commercial source of astaxanthin. The deep sea species Aristeus alcocki can thus be considered as a better source of astaxanthin for commercial exploitation than Pandalus borealis. TLC analysis of the shell waste extract showed that it contains free astaxanthin, astaxanthin monoester and astaxanthin diester in the ratio 1:1:2. GLC identification of the fatty acids esterified with astaxanthin revealed that saturated fatty acids, MUFA and PUFA are in the ratio 5:3:2 in monoester, whereas in diester they are in the ratio 4:3:3. The main fatty acids in monoester and diesters are palmitic acid, oleic acid, stearic acid and PUFAs: DHA and EPA. The in vitro antioxidant activity of the astaxanthin extract showed significant hydroxyl radical scavenging activity, superoxide anion scavenging activity and inhibition of lipid peroxidation. The IC50 values obtained were 56.43 ± 1.06 ng/ml, 27.91 ± 0.54 ng/ml and 26.54 ± 0.42 ng/ml, respectively. The antioxidant activity of astaxanthin from Aristeus alcocki was obtained at nanogram levels. This powerful antioxidant function may be due to the unique molecular structure of astaxanthin and synergistic effect of astaxanthin and PUFAs present in the astaxanthin monoester and diester fractions. The astaxanthin extract from shrimp shell waste significantly reduced carageenan induced paw edema in mice, percentage inhibition being 47.83 and 67.11 percent at astaxanthin concentrations of 0.5 mg/kg body weight and 1.0 mg/kg body weight, respectively. The inhibition of inflammation at 1.0mg/kg body weight was greater than that produced by the standard reference drug diclofenac. Cardioprotective effect of astaxanthin was examined in isoproterenol induced myocardial infarction in rats. Levels of diagnostic marker enzymes, LDH, CPK, GOT, GPT, CK, CK-MB in plasma, lipid peroxides, ascorbic acid, reduced glutathione and the activities of glutathione-dependent antioxidant enzymes GPx, GR, GST and antiperoxidate enzymes CAT, SOD and the membrane bound enzyme Na+ - K+ ATPase in the heart tissues of experimental groups of rats were determined. The prior administration of astaxanthin @ 10mg/kg feed for 45 days significantly prevented the isoproterenol-induced elevation in the levels of diagnostic marker enzymes in plasma, induction of lipid peroxidation and alterations in the level of reduced glutathione and in the activities of glutathione dependent antioxidant enzymes and antiperoxidative enzymes of experimental rats. Feeding astaxanthin caused a decrease in the inhibition of Na+ - K+ ATPase activity against isoproterenol induced myocardial infarction. The powerful cardioprotective effect of astaxanthin can be attributed to the multiple independent mechanisms viz. antioxidant effects, singlet oxygen quenching ability and inhibition of lipid peroxidation of membranes, increased functional gap junctional intercellular communication, anti-inflammatory effects etc. Immunostimulatory action of astaxanthin extract was evaluated in experimental mice. Astaxanthin administration was found to enhance the proliferation of spleen cells and bone marrow cells. Esterase activity was found to be enhanced in bone marrow cells indicating increased maturation of cells of lymophoid linkage. Astaxanthin also enhanced number of antibody forming cells and circulating antibody titre. Thus astaxanthin exhibits strong immunomodulating properties. A significant reduction in the viability of ascites tumour cells DLA in vitro was noted in the current study. The % viability was reduced to 4.34 % at a concentration of 15μg astaxanthin/ml. The cytotoxic action of astaxanthin against DLA may be through induction of apoptosis or through a different pathway. Antitumour activity of astaxanthin was studied by ascite and solid tumour models in mice. An increase in life span of about 67 % was noted in DLA bearing mice administered with astaxanthin at 5 mg/kg body weight. The tumour volume and tumour weight were significantly lower in mice injected with 5 mg/kg body weight astaxanthin. In vitro studies revealed that astaxanthin from shrimp shell waste of Aristeus alcocki inhibited the proliferation of cervical cancer cells HeLa in a dose dependent manner.ThesisItem Open Access Genetic characterization, controlled breeding and development of transgenic varieties of puntius denisonii (day, 1865).(Department of Aquaculture, College of Fisheries, Panangad, 2010) Manoj, C K; KAU; Mohanakumaran Nair, CPuntius denisonii, a beautiful ornamental fish indigenous to the Western Ghats, which has been indiscriminately exploited from the different rivers of Kerala has been recently declared to be vulnerable by the IUCN. The population structure and genetic diversity of P. denisonii has not yet been studied and documented. Many previous attempts to breed this fish in captivity have yielded negative results. The increasing demand for this fish to decorate aquariums worldwide could be satisfied only by developing controlled breeding techniques and larval rearing of its fry. In the present study, the present population structure of P. denisonii has been studied combining both phenotypic and genotypic techniques. Fishes were collected from Irrity, Chaliyar and Periyar rivers of Kerala. Truss network analysis was conducted and the size adjusted morphometric variables were subjected to Principal Component Analysis and Canonical Variance Analysis. Scatter diagram and Dendrogram was plotted using PCA and CVA loadings. The Irrity and the Chaliyar populations were grouped on the positive sector of the PC and CV component showing morphological similarities between the two populations while the Periyar population was placed in the negative sector of the component separated far from the other two. The PC scores were used to find out the variables showing maximum variation between fishes collected from different rivers. RAPD PCR was conducted after isolating DNA from the fins of different populations of P. denisonii. Universal random primers were screened and the primers that produced reproducible bands were selected. Popgene analysis of the binary data yielded the genetic structure of different populations of P. denisonii. Number and percentage of polymorphic loci, Nei's (1973) gene diversity, Shannon's Information index Lewontin (1972), Nei's Unbiased Measures of Genetic Identity and Genetic distance and Dendrogram Based Nei's (1978) Genetic distance using UPGMA --Modified from NEIGHBOR procedure of PHYLIP Version 3.5 were studied. The results obtained supports the truss analysis in that the Irrity and Chaliyar populations in Northern Kerala are genetically more similar while that of Periyar population in Central Kerala are distinct. P. denisonii was successfully induced bred under controlled conditions with synthetic hormone preparations Ovaprim and WOVA-FH. Stress during transport and handling was minimized and live feed was supplemented to enhance maturation of the broodstock. The whole developmental sequence starting from fertilized eggs to hatching was photographed and documented. It took 29-30 hours for the eggs to hatch at 280C. Rearing of fry was successfully accomplished under laboratory conditions. In an attempt to develop transgenic varieties of P. denisonii, pCMV-GFP was electroporated into newly fertilized eggs, maintained in hypoosmolar electroporation buffer. The electroporation parameters that yielded best results were 20V, 3 bursts at 1 second interval. Fin clips were taken from the transgenic individuals reared for a period of 6 weeks. Dot blot test was positive showing integration of the GFP gene in P. denisonii, eventhough expression was not detected under blue or UV light. The genetic and phenotypic data of P. denisonii populations in the present study will aid as a base line for formulating conservation procedures to protect the genetic diversity of wild ones. Stock identification studies are recommended for more concise information on each population. Moreover, the larval rearing and controlled breeding techniques along with the genetic diversity studies will help to design captive breeding programs and enhance the production of hatchery bred ones to meet increasing demand. Further research is recommended for generating transgenic lines with uniform GFP expression.ThesisItem Open Access Heterosis breeding in sesame (Sesamum indicum L.).(Department of Plant Breeding and Genetics, College of Horticulture, Vellanikkara, 2011) Gayathri, G; KAU; Dijee, BastianThe study entitled ‘Heterosis breeding in sesame (Sesamum indicum L.)’ was undertaken at the Department of Plant Breeding and Genetics, College of Horticulture, Vellanikkara. The objectives of the study were to collect and evaluate different genotypes of sesame for morphological traits and yield attributes, to identify useful parents producing heterotic crosses and developing hybrids in sesame. The study also intended to develop male sterile lines in sesame through interspecific hybridization with Sesamum malabaricum. Sesamum indicum and Sesamum malabaricum accessions were collected from Kerala and Tamil Nadu and evaluated for their morphological traits. Wide range of variation was noticed for characters like plant height, number of days to flowering and seed yield per plant which contributed maximum to genetic divergence. The genotypes studied were grouped into six clusters. High genotypic coefficient of variation (GCV) was recorded for number of capsules per plant, plant height, seed yield per plant and number of branches per plant. High heritability with high genetic advance as per cent of mean was recorded for number of days to flowering, plant height, number of branches per plant, number of capsules per plant and seed yield per plant. This indicates that the characters are governed by additive gene effects and selection for these traits will be effective. Association analysis revealed that seed yield per plant was correlated to plant height, number of capsules per plant and number of days to flowering. Path coefficient analysis indicated maximum positive direct effect by number of capsules per plant, capsule length, plant height and 1000 seed weight on seed yield per plant. In order to develop hybrids, fourteen parents were selected based on the per se performance of the genotypes. They were crossed in line X tester mating design. Forty eight hybrid combinations obtained were raised in the field along with the parents and evaluated for their heterosis and combining ability effects. Parental genotypes AVTS-06-5, AVTS-06-10, IVTS-06-12, KYM-1, Tilak and TMV-6 were identified as high combiners based on general combining ability (gca) effects. Two combinations viz. AVTS-06-5 X KYM-1 and IVTS-06-12 X TMV-3 had significant values of per se performance, specific combining ability (sca) effects and standard heterosis for seed yield per plant. They can be evaluated for their hybrid vigour over locations and seasons. The crosses AVTS-06-5 X TMV-3, AVTS-06-5 X TMV-6 and TCR 3279A X KYM-1 have been identified as potential cross combinations for isolation of promising segregants as the parents involved in these crosses had high significant gca effects for seed yield per plant but the hybrids recorded non significant sca effects. Interspecific hybridization between S.malabaricum and S.indicum was attempted to develop male sterile lines. Seed set was noticed in three interspecific hybrids which failed to germinate due to embryo abortion. Hence these embryos were rescued and raised in vitro to obtain the hybrids.ThesisItem Open Access Characteization and evaluation of nutmeg (Myristica fragrans Houtt.) accessions(Department of Plantation Crops and Spices, College of Horticulture, Vellanikkara, 2016) Vikram, H C; KAU; Mini Raj, NNutmeg (Myristica fragrans Houtt.) is an introduced crop to India. There exists tremendous variability in the nutmeg population in Kerala, which is the major nutmeg growing state in the country. Assessment of the existing variability is a prerequisite for taking up successful crop improvement programmes, which is very much limited in this tree spice. In this context, the present study entitled “Characterization and evaluation of nutmeg (Myristica fragrans Houtt.) accessions” was taken up exclusively with the specific objectives to characterize nutmeg accessions based on morphological, biochemical and molecular parameters so as to scale the variability in a multidimensional way. Select fifty nutmeg accessions from a core germplasm collected and maintained in a private plantation in the Chalakudy river basin, belonging to age of fifteen years, formed the material for the study. Among the select fifty accessions, forty two were females, four monoecious and four males. In the morphological characterization, 51 qualitative and 38 quantitative characters were recorded from two trees per accession. Biochemical characterization was done in the select seventeen distinct accessions. GC-MS profiling was done in kernel and mace oils. Biochemical constituents of fresh pericarp were estimated. Isozyme profiling was done for peroxidase and polyphenol oxidase enzymes. The molecular characterization was attempted with 21 RAPD and 12 ISSR primers after screening. A key for identification of an elite nutmeg tree was developed. A descriptor for nutmeg with a set of 51 qualitative and 38 quantitative parameters and descriptor states for each of these characters was developed as the first step. This is the first study of its kind to develop a minimal descriptor for nutmeg. The descriptor developed from the present study was simultaneously utilised for morphological characterization and evaluation of the accessions. Wide variability was noticed among the accessions for 47 out of 51 qualitative characters. Four characters viz., leaf margin, fruit pubescence, grooves on nut and nature of fruit dehiscence were noted as non variable characters and hence, these were not included for further analysis. Based on the qualitative characters, accessions were classified into 11 clusters at 66 per cent similarity level. Accessions differed significantly for all the quantitative characters except shelling percentage. Performance evaluation of the accessions brought out the superiority of accession 8, 9 and 22 for yield. The accessions showed high GCV, PCV, h2 and genetic gain for most of the characters. Number of fruits per tree, fruit set percentage, number of fruits per m2, fresh and dry weight of mace, mace volume as well ratio of nut to mace exhibited high genetic gain. Hence, selection programme based on these characters will be very effective in improving the base populations. Based on Mahalanobis D2 analysis, accessions were grouped into 10 clusters. Wide range of variation was observed in contents of volatile oil, oleoresin and fixed oil of kernel and mace. Based on these constituents accessions were grouped into 26 clusters, which indicated their distinct quality. Based on the results of the morphological characterization, seventeen distinct accessions were selected for further biochemical and molecular analysis. GC-MS analysis of kernel and mace oils exhibited 20 and 24 constituents respectively. Volatile oil composition exhibited wide variability for the major constituents viz., myristicin, elemicin, safrole and sabinene apart from the presence of some unique compounds. Grouping of the accessions was done based on the per cent content of these important compounds. Two accessions recorded high contents of both myristicin and elemicin whereas another two accessions were in the complimentary; belonging to low myristicin group. High sabinene combined with low myristicin was the intrinsic quality attribute of one of the accessions. Change, as well as addition/deletion of specific constituents was also noticed in the volatile oils after storage for one year. Accessions exhibited wide range of variation in the biochemical constituents of pericarp, a valuable information for the value addition of pericarp. Total phenol and tannins exhibited high variation. The accessions were ranked based on the content of biochemical constituents. Isozyme profiling using peroxidase enzyme produced four bands and that based on polyphenol oxidase exhibited three bands. Molecular markers could assess the variability among the accessions. The selected 21 RAPD primers produced a total of 164 amplicons of which 63.21 per cent were polymorphic. The 12 ISSR primers selected produced a total of 87 amplicons of which 69.44 per cent were polymorphic. Few unique bands were detected for specific characters. Inter cluster association of each of the qualitative clusters with other clustering patterns was worked out. The results indicated the differences as well as similarities of the qualitative clusters with other clustering patterns. Finally, key quantitative characters were identified based on their direct and indirect effect on yield as also economic importance. The statistical key thus developed using 13 key quantitative characters will serve as a preliminary tool for identification of an elite nutmeg tree.ThesisItem Open Access Groundwater irrigation: management, adaptation and economic costs under declining resource conditions(Department of Agricultural Economics, College of Horticulture, Vellanikkara, 2017) Seenath Peedikakandi; KAU; Indira Devi, PGroundwater is the major source of domestic use and irrigation in Kerala, accounting for 39 per cent of net irrigated area. Irrigated agriculture in the state shows continuous increase over years. At the same time Kerala is reported as third among the states with highest depletion of groundwater. This situation poses challenges in agricultural production. The study ‘Groundwater irrigation: Management, adaptation and economic costs under declining resource conditions’ was undertaken, in this background. The objectives of the study were to analyse the extent of decline in groundwater resources and farmers’ understanding of the same, to analyse the extraction practices, management and economic efficiency of groundwater irrigation and coping (short term) and adaptation (long term) strategies towards management of groundwater decline and the economic cost of adaptation strategies. The study was conducted in Palakkad district of Kerala. Based on the stage of ground water development, three Block Panchayats viz., Chittur (over exploited), Malampuzha (critical) and Pattambi (semi-critical) were selected for the study. 50 Open Well (OW) irrigated and 50 Bore Well (BW) irrigated farms from each BP were randomly selected from the Grama Panchayats (GPs) where observational wells of the GWD (Ground Water Department- Kerala) are situated. Primary data was collected from the sample farms through field visits using pre-tested structured interview schedule and through direct observation. PRA (Participatory Rural Appraisal) was also conducted in each BP to draw the time line of changes in ground water status and social perceptions. Secondary data on monthly water levels of Groundwater Monitoring Wells (GMWs) maintained by GWD (Palakkad),rainfall data and published reports were used for the study. Statistical tools like descriptive analysis, regression and Stochastic Frontier Function were employed for analysis of the data. In most of the GMWs in the study area, the Water Level from Ground (WLG) has been declining over the years. The trend was more predominant during early summer (Dec.–Jan.) in Chittur and Malampuzha and in late summer in Pattambi BP. Regression analysis showed that WLG was significantly influenced by one year lagged rainfall in Chittur and current year rainfall in Malampuzha and Pattambi. The average well density was 205/km2 with highest in Pattambi. Density of defunct wells was highest (45/km2) and the average functional age of bore wells was lowest (7 years) in Chittur. The depth of well was highest in Chittur where bore well depth (136 mbgl- meters below ground level) was double than that of Pattambi. Coconut based cropping system was prevalent in most of the farms except in Malampuzha where paddy was the major crop. Flood, basin and sprinkler irrigations were found to be more common in Malampuzha and Pattambi BPs, while drip irrigation was prevalent in Chittur. Cost of irrigation in Chittur was about Rs. 29,000/ha/year which accounted for 37 per cent of cost of cultivation. Annual net return per ha. of farm was lowest (Rs. 17,640/-) in Chittur due to low cropping intensity. Stochastic Frontier Analysis indicated that mean economic efficiency was high (99.9%) in Chittur as most of the farms were functioning along the cost frontier. The variability among the farms in Chittur was low. Respondents opined that groundwater is declining over the years irrespective of the region. It has been so, for more than a decade in Chittur affecting socio-economic well-being of farmers. They attributed intensive extraction through bore wells and low rainfall as the major reasons for the decline. Farm level adaptations to water scarcity are classified under ‘supply management’ (methods that facilitated increase in quantity of water available for irrigation) and ‘demand management’ (methods that tried to use the water effectively through minimizing the use) strategies. The supply management strategies were mainly exploitative in nature which included digging new bore well (52-58%), improved draft technology with compressor pumps (58%), taking pits for water conservation (7%), coconut husk burial (12%), coconut leaf mulching (18%) and dependence on water markets (8%). Digging new bore well was the most common supply management strategy in Chittur which is highly capital intensive. The average cost amounted to Rs. 8,520/ha/year. Intensive extraction was done by excessive use of subsidized electricity. Adoption of drip irrigation (60%) was the most widely practiced demand management strategy which cost about Rs. 22,000/ha/year. Cropping pattern change from paddy and sugarcane to coconut was also observed. About 18 per cent of the land area in Chittur was kept fallow due to water scarcity. The study brings out results that suggest policy interventions in regulating bore well digging and revisiting the power subsidy system. In Chittur area, where the rainfall is scanty, extension of the Right Bank Canal of the Chittur River irrigation project is the most feasible solution. Taking up on-farm research trials in the area to suggest efficient farming systems and practices may also be done. Simultaneously water resource conservation strategies are to be popularized through awareness creation, capacity building programmes and subsidy support.ThesisItem Open Access Development of F1 hybrids of indeterminate tomato (Solanum lycopersicum L.) for protected cultivation(Department of Olericulture, College of Agriculture, Vellayani, 2015) Lekshmi, S L; KAU; Celine, V AThe present investigation entitled “Development of F1 hybrids of indeterminate tomato (Solanum lycopersicum L.) for protected cultivation” was conducted at the Department of Olericulture, College of Agriculture, Vellayani, from 2013 to 2015 with the objectives of identifying superior varieties and developing F1 hybrids of indeterminate tomato suited for protected cultivation. The study consisted of two experiments conducted in the naturally ventilated polyhouse of size 50 m x 20 m located at the Instructional Farm, Vellayani. In the first part of the first experiment, 40 tomato genotypes were evaluated for two consecutive years in an RBD with three replications. As the second part, 12 commercial hybrids were evaluated. The second experiment consisted of a 9 x 9 half diallel analysis laid out in an RBD with three replications. Analysis of variance showed significant differences between the genotypes for all the characters for two crops. Pooled analysis revealed that, LE 1 recorded the highest yield (2443.43 g) and fruit weight (108.13 g) followed by LE 7. LE 53 had maximum number of fruits per plant (65.00). In the present study, genotypes had wide variation for quality parameters. Fruits of LE 14 recorded highest TSS with a mean of 5.74 ºBrix. LE 7 had maximum ascorbic acid (30.13 mg/100g) and lycopene content (13.09 mg/100g). Beta carotene value was maximum in LE 16 (184.15 mg/100g). There was minimum incidence of pests, diseases and physiological disorders under protected conditions. Among the 12 hybrids evaluated, INDAM 9802 was the highest yielder (1444.40 g) followed by F1 T 30 (1412.22 g). F1 T 30 recorded maximum fruits per plant (35.66) which was on par with F1 Queen (35.55). Genetic parameters like phenotypic and genotypic coefficients of variation, heritability and genetic advance were studied to assess the genetic variability among the genotypes. High heritability coupled with high genetic advance were observed for characters like truss per plant, fruits per truss, fruit weight, fruits per plant, yield per plant and yield per plot. Path analysis revealed highest positive direct effect for fruit weight (0.3956), truss per plant (0.3558) and fruits per plant (0.3381). Based on D2 analysis the 40 genotypes were grouped into eight clusters. Cluster I was the largest with twenty four genotypes followed by cluster II with ten genotypes. Diallel analysis was carried out using nine parents selected based on genetic divergence and per se performance. The parents were crossed in a diallel fashion excluding reciprocals to obtain 36 F1 hybrids. The study revealed that P5 x P9 had the highest yield (3114.03 g) which was on par with P6 x P8 (3074.37 g) and P1 x P5 (3077.58 g). P1 x P5 had the maximum fruits per plant (103.93). The magnitude of relative heterosis, heterobeltiosis and standard heterosis varied considerably. For yield, relative heterosis ranged from -32.40 to 92.72, heterobeltiosis from -47.14 to 89.54 and standard heterosis from 2.91 to 160.95. The σ2gca and σ2sca ratio indicated that non-additive gene action was predominant for all traits. Among the nine parents, P9 (LE 1), P5 (LE 20) P1 (LE 2), and P2 (LE 7) were superior for yield and yield attributes. The estimates of sca effects indicated that P5 x P9 (LE 20 x LE 1), P6 x P8 (LE 39 x LE 38) and P1 x P5 (LE 2 x LE 20) were the most promising hybrids for protected cultivation. The present study revealed that the genotypes LE 1 and LE 7 and the hybrids INDAM 9802 and F1 T 30 were superior for yield and yield attributes under protection. Based on the mean performance, standard heterosis and sca effects the three potential crosses viz., P5 x P9, P6 x P8 and P1 x P5 could be adjudged as suitable indeterminate tomato hybrids for protected cultivation.ThesisItem Open Access Detergent potential of enzymes of dairy microflora and their effect on the shelf life of milk products(Department of Dairy Science, College of Veterinary and Animal Sciences, Mannuthy, 2010) Beena, A K; KAU; Geevarghese, P IA study was conducted to assess the detergent potential of a spoilage protease enzyme obtained from the microflora of dairy plant environment. An attempt was also made to study the impact of selected enzyme producers on the shelf life of curd (dahi) and sterilised skim milk. A total of 71 bacterial isolates obtained from dairy environment were screened for their ability to produce spoilage enzymes like proteases lipases and lecithinases. Based on the spoilage potential, Pseudomonas aeruginosa (P12) isolated from pasteurised milk and Bacillus cereus (S4) isolated from sterilized skim milk were selected for further work. The influence of spoilage enzymes on selected physico-chemical characteristics of curd (dahi) and sterilized skim milk was evaluated by preparing the products from milk precultured with isolate P12 and S4. In general, proteolysis of milk was found to have an adverse effect on the quality of products. The stimulatory effect of proteolytic products of P12 and S4 on curd starters was evident from the higher values of acidity, firmness and syneresis in treated curd. The spoilage enzymes adversely affected the overall quality and shelf life of curd. In treated sterilised milk, tyrosine and NPN values were highly elevated. A linear correlation was found to exist between off-flavour and proteolysis. Curd and sterilised skim milk prepared from milk precultured with proteolytic organism were significantly different from that of control. The possibility of exploiting an alkaline protease from spoilage organism in dairy plant sanitation was also looked into. Environmental conditions for the production of alkaline protease by a psychrotrophic strain of Bacillus cereus (S4) was optimised in whey based medium. The protease used in this trial preferred an alkaline medium to remain stable. The enzyme was found to be stable over a wide temperature range of -10°C to 80°C and a pH range of 7.0 to 12.0. The metal ions Ca++, Mg++, Zn++ and Hg++ enhanced the enzyme activity. Lack of inhibition by Hg++ suggested lack of disulphide bonds in the active site of enzyme. Significant inhibition of activity by serine inhibitors indicated an essential serine residue in the active site of enzyme. The deleterious effect of EDTA on enzyme activity showed the supportive role of divalent cations. Marked residual activity on treatment with β-mercaptoethanol indicated the absence of cysteine residue for the enzyme. Enhancement of protease activity in the presence of surfactants and stability in the presence of H2O2 signified its potential to be used as detergent additive. Qualitative assessment of cleaning efficiency of inbuilt formulation substantiated the superiority of enzyme based formulations. Ammonium sulphate fractionation, dialysis and gel filtation using seralose 4B and Seralose 6B were effective in purifying the protease preparation by 141.31 fold. The purified protease was found to be a homogenous preparation of molecular weight of 50.5 kDa as determined by SDS PAGE.ThesisItem Open Access Development and evaluation of different vaccines against duck pasteurellosis(Department of Dairy Science, College of Veterinary and Animal Sciences, Mannuthy, 2010) Jesto, George; KAU; Krishnan NairThis study was undertaken to develop biofilm vaccines against duck pasteurellosis using oil, saponin and aluminium hydroxide as adjuvants and to experimentally evaluate their immunogenicity in ducks. Identity of P. multocida serotype A: 1 (DP1) used for study was confirmed by biochemical tests and by PM-PCR and pathogenicity was established in Swiss albino mice before vaccine production. The LD50 (11 w) of the DP1 isolate determined was 10 CFU / bird and MDT was 23.75 h in 11 week old ducklings when a high dose of 3 X 10 6 CFU of P. multocida per bird was given. At 11 Weeks age MDT gradually increased as the dose of inoculum decreased. In 21 week old ducks, the LD50 (21w) of the isolate DP1 was estimated to be 3 ×108 CFU of P. multocida and it showed that the Kuttanad duck had decreased susceptibility to pasteurellosis with age. On light microscopic studies planktonic cells appeared to be Gram negative coccobacillary, while biofilm cells were Gram negative and pleomorphic. Electron microscopic studies revealed that P. multocida could form well differentiated classic biofilm and 0.32 per cent TSB media supplemented 0.5 per cent chitin seemed to be excellent medium for biofilm formation by P. multocida. Four different vaccines viz. OV, OBV, SV and SAV were prepared and all of them were found to be sterile and safe. The oil adjuvanted vaccines (OV and OBV) offered better protection compared to saponin and aluminium hydroxide adjuvanted vaccine groups (SV and SAV) following primary vaccination, up to seven weeks. The modified oil adjuvanted vaccine prepared was not only found to be homogenous, but also more efficient in stimulating a humoral immune response and hence may be recommended. The oil adjuvanation gave better protection than saponin and aluminium hydroxide adjuvanation. The SAV gave better protection than SV which might be due to the presence of aluminium hydroxide which potentiated the immunostimulating ability of saponin. The combined vaccine (SAV) although was found to be better than single vaccine (SV) they cannot be used as a substitute to oil adjuvanted vaccines. The booster vaccination was found to have added advantageous effect on protection and is a must, to prevent losses. Pasteurella biofilms although found to be weak in inducing a primary immune response had the potency to evoke a more powerful secondary response compared to planktonic cells. Vaccination done at six weeks age followed by booster vaccination at 16 weeks age seemed to be a better modification of existing schedule and may be recommended. In histopathological studies, lymphoid hyperplasia was observed in spleen in survived control birds and in SV and SAV vaccine groups that did not survive challenge test, which indicated the persistence of Pasteurella organisms through mild infection in them following experimental challenge. Lymphoid depletion was observed in caecal tonsil in experimental pasteurellosis as in spleen. As the survived vaccinated birds following challenge test showed normal intact caecal tonsil, the course of disease and lesions might be less prominent in vaccinated birds during infection process. The well developed bursa observed in OV and OBV birds that survived challenge test indicated that the humoral immune response was well induced in them compared to other groups. The designed primers E1 and E2 amplified the gene E and hence, this pair of primers could be used for the production of amplified Gene E sequences for further studies on recombinant ghost system. In conclusion, 0.32 per cent TSB media supplemented 0.5 per cent chitin seemed to be an excellent medium that support classical biofilm formation by P. multocida. Booster vaccination definitely had added advantageous effect on protection. Immunization at 6 weeks of age with OV followed by booster vaccination at 16 weeks age with OBV seemed to be a better modification of existing schedule and may be recommended. In histopathological studies, the lesions were less prominent in vaccinated birds than control birds which indicated that the vaccines were effective.
