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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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    Institutional PublicationsItemOpen Access
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    Institutional PublicationsItemOpen Access
    Mannual on pressurised irrigation
    (Kerala Agricultural University, Vellanikkara, 2008) Jippu, Jacob; KAU
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    Institutional PublicationsItemOpen Access
    പൊക്കാളി കര്‍ഷകസംഗമവും നിര്‍ദ്ദേശങ്ങളും
    (Kerala Agricultural University, Vellanikkara, 2008) Anilakumar, K; KAU
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    Institutional PublicationsItemOpen Access
    Agriculture development in an emerging non agrarian regional economy : Keralas challenges
    (Kerala Agricultural University, Vellanikkara, 2008) Kannan, K P; KAU
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    ThesisItemOpen Access
    Evaluation of hepatoprotective effect of ethanolic extract of eugenia jambolana (njaval) leaves on paracetamol induced toxicity in rats
    (Department of Pharmacology and Toxicology, College of Veterinary and Animal Sciences Mannuthy, 2008) Midhun, M V; Aravindakshan, C M
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    ThesisItemOpen Access
    Enhancement of propagation efficiency in exotic varities of heliconia
    (Department of Pomology and Floriculture, College of Agriculture, Vellayani, 2008) Reshmi, C R; KAU; Sheela, V L
    Heliconias are among the most popular garden plants, both for the ease with which they can be grown and the sheer magnificence of the blooms. Studies were conducted to standardize rapid propagation techniques under in vitro and in vivo conditions. Three heliconia varieties belonging to three distinct groups viz., St. Vincent Red (small erect type), Golden Torch Adrian (hybrid) and Sexy Pink (large pendent type) were selected for the study. For in vitro culture establishment, shoot tip explants were effective. The treatment of shoot tips with 0.10 per cent mercuric chloride for ten minutes followed by dipping in 0.05 per cent mercuric chloride for five minutes (after trimming) resulted in better surface sterilization. Longitudinal cutting of the in vitro established shoot tip with apical dome into two halves and culturing them separately produced the highest number of axillary buds. Addition of 0.05 per cent activated charcoal to the establishment media reduced the media browning and hastened shoot initiation. For culture establishment of all the three varieties, MS medium supplemented with BA 5.00 mg l-1 was found to be the best. Murashige and Skoog medium supplemented with BA 2.00 mg l-1 resulted in the highest shoot proliferation in the variety St. Vincent Red. In Golden Torch Adrian, BA 2.00 mg l-1 + NAA 0.20 mg l-1 gave better results. In the variety Sexy Pink, Kinetin 5.00 mg l-1 + NAA 0.20 mg l-1 was the best. For further multiplication in Sexy Pink, BA 1.00 mg l-1 was sufficient. Solid culture medium was better for shoot proliferation in the variety Sexy Pink. Higher sucrose concentration (40.00 g l-1) increased the multiplication rate, but reduced the length of shoots as well as the number of leaves. Addition of activated charcoal to the media as well as exposure of cultures to light had negative effect on shoot proliferation. Full MS medium was found to be the best for in vitro rooting of the variety Sexy Pink. Addition of NAA 0.50 mg l-1 to the MS medium gave better results for in vitro rooting in Golden Torch Adrian and Sexy Pink. Sucrose @ 30.00 g l-1 was sufficient for in vitro rooting in the variety Sexy Pink. Activated charcoal delayed root initiation and reduced the number of roots in the variety Sexy Pink. Sand recorded 90.00 per cent survival in all the three varieties after two months of planting out. At varietal level, significant difference was evident in the total number of suckers. In the first experiment, the variety St. Vincent Red (3.82) was significantly superior in terms of total number of suckers. However, in the second experiment, St. Vincent Red (4.06) was on par with Golden Torch Adrian (4.10). The variety Sexy Pink produced comparatively taller suckers in both the trials. Varietal variation in the number of leaves was observed only in the earlier stages. During the preliminary field experiment, the variety Sexy Pink excelled in leaf area at almost all stages of observation. Among the three varieties, highest collar girth was recorded by suckers of Sexy Pink variety during the first two stages of observation. However, towards the later stages, it was statistically on par with St. Vincent Red. Foliar spray was superior to rhizome dip in terms of total number of suckers, height of suckers and the number of leaves. In the case of leaf area, both the treatments were more or less on par. Application of growth regulators had pronounced effect on sucker production at all the stages during the first experiment when BA 750 mg l-1 produced the highest number (4.19) of total suckers. In the second experiment, variation was evident only in the total number of suckers. Here, BA 850 mg l-1 produced the highest number (4.33) of suckers and it was on par with BA 700 mg l-1 (4.00) and GA3 650 mg l-1 (3.79). Irrespective of the stage of plant growth, gibberellic acid produced taller suckers and BA 500 mg l-1 resulted in the shortest suckers. BA treatments recorded comparatively higher number of leaves. Growth regulator application had remarkably influenced the leaf area of suckers also. Application of BA 1000 mg l-1 (3.53 cm) and GA3 800 mg l-1 (3.33 cm) recorded higher collar girth in suckers. VG interaction exerted significant variation in the number of suckers. At varietal level, BA 750 mg l-1 produced the highest number of suckers in St. Vincent Red (4.75), GA3 500 mg l-1 in Golden Torch Adrian (4.63) and GA3 750 mg l-1 in Sexy Pink (4.00). Among VG treatment combinations in the second experiment, the highest number of suckers (4.75) in the variety St. Vincent Red was produced by BA 700 mg l-1. The varieties Golden Torch Adrian (4.88) and Sexy Pink (3.75) recorded the highest with BA 850 mg l-1. Gibberellic acid produced taller suckers. In the second experiment, VG interaction had no significant effect on the height of suckers. Regarding the number of leaves, BA resulted in comparatively higher number of leaves in both the experiments. In all the three varieties, BA 850 mg l-1 produced the highest number of leaves. Collar girth was found to increase with increase in the concentrations of BA and GA3 in all the three varieties. The economics of foliar application of growth regulators revealed that BA 850 mg l-1 significantly enhanced the profit in the varieties Golden Torch Adrian and Sexy Pink. Although negligible, BA 700 mg l-1 recorded slight positive response in the variety St. Vincent Red with respect to profit.
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    Institutional PublicationsItemOpen Access
    College magazine students’ union 2007-’08
    (College of Horticulture, Vellanikara, 2008) KAU
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    ThesisItemOpen Access
    Comparative evaluation of membrane protein and biofilm vaccines against duck pasteurellosis
    (Department Of Poultry Sciences,College of Veterinary and Animal Sciences, Mannuthy, 2008) Indu, K; KAU; Krishnan Nair, C
    A research work was undertaken to prepare effective vaccines against P. multocida grown under different conditions and assess their immunopotency in one month old ducklings. The purity of the Pasteurella multocida A: 1 strain (DP1) and A: 4 strain (PA4) was confirmed as per standard procedures. Pathogenicity of DP1 and PA4 was assessed in six to eight week old mice. The isolates killed the intraperitoneally inoculated mice within eight hours and within 24 h when injected by subcutaneous route. Pasteurella multocida A: 1 was used for the preparation of different vaccines. The organism was grown in BHIB for preparation of ordinary bacterin. The in vitro biofilm formation of the organism was assessed by growing it under nutrient restricted conditions. For this, the organism was grown in TSB (0.32 per cent) supplemented with 0.3 per cent bentonite clay. For preparation of OMP suspension, the organism was grown in iron restricted condition viz., BHIB supplemented with 100 µM 2, 2’ Dipyridyl and the OMPs were extracted using sodium lauryl sarcosinate. The protein concentration of OMP suspension was estimated to be 3 mg/ml. Median lethal dose (LD50) of DP1 was 10-7.5, which contained 32 viable cells/ ml and that of PA4 was 10-7.38, which contained 24 viable cells/ ml when determined in one month old ducklings. Oil adjuvant vaccines were prepared using ordinary bacterin, bacterin made from biofilm and OMP suspension and performed the sterility, safety and potency tests of the vaccine employing standard procedures. A total of 260 four week old ducklings were divided into four groups with 65 birds in each group and the first three groups were vaccinated with ordinary bacterin, OMP vaccine and biofilm vaccine respectively. The fourth group served as control. The birds were vaccinated with 0.5 millilitre of vaccine intramuscularly in the thigh region. Blood was collected from all the ducks pre-vaccination, at weekly intervals upto 3 weeks post vaccination (PV) and then at 15 days interval upto 60 days, by cardiac puncture or by jugular venipuncture. Passive haemagglutination using GA-SRBC sensitized with sonicated antigen of DP1 was used to measure the humoral immune response. The IHA titres obtained for biofilm vaccine group on day 14 was very much higher than the other two groups. The antibody titre was observed from day seven onwards for all the groups. All the vaccine groups have shown significant difference from the control group at all the stages of the study. On homologous challenging, biofilm vaccine gave higher protection rates of 80 per cent than the 70 and 50 per cent protection rates of ordinary bacterin and OMP vaccine respectively, when challenged with 100 LD50 dose on day 20 PV. On day 60 PV, biofilm vaccine gave higher protection rate of 70 per cent than the 60 and 50 per cent protection rates respectively of ordinary bacterin and OMP vaccine, when challenged with 100 LD50 dose. On heterologous challenging, biofilm vaccine gave higher protection rates of 70 per cent, while only 50 per cent protection was afforded by both bacterin and OMP vaccine, when challenged with 100 LD50 dose on 20 day PV. On day 60 PV, biofilm vaccine gave higher protection rate of 60 per cent while both the other vaccines gave only 50 per cent protection, when challenged with 100 LD50 dose. All the birds challenged on day 40 PV, either with homologous and heterologous organisms died. In most cases, the death occurred due to coliform infection along with stressful factor such as increased atmospheric humidity due to heavy rainfall at that time. In few cases, birds died due to pasteurellosis which might be due to lack of protective level of antibody titre. Biofilm vaccine proved to be the best among the three vaccines tried. Further field trials are to be done before advocating this vaccine for commercial use.
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    ThesisItemOpen Access
    Growth and survival of penaeus monodon in monosex and mixed sex culture under laboratory condition
    (Department of Aquaculture, College of Fisheries, Panangad, 2008) Bajaniya Viralkumar, Chhaganlal; KAU; Mohanakumaran Nair, c
    Sexual dimorphism is apparent in the black tiger shrimp, Penaeus monodon with females achieve larger size than the males. This character may be attributed to behavioral and/or physiological differences between the sexes. An experiment was developed to determine if there were advantages in rearing all female or all male P. monodon as opposed to mixed-sex populations. Juvenile shrimps (4.46±0.54 g) were collected from earthen pond and individually hand sexed and stocked in the circular cement tanks. Treatments all male, all female and mixed-sex were stocked @ 8 nos./tank. Each treatment had five replicates. The shrimps were offered commercial shrimp feed. The experiment was conducted for a period of 50 days. At harvest, all female shrimps had shown significantly higher growth than all male and mixed-sex treatment. Survival was not significantly different among treatments. FCR of all female was significantly lower than the all male and mixed-sex treatment. Result of the present study demonstrates a benefit to all female culture of P.monodon against the all male or mixed-sex culture. Thus culture of all female may be commercially more attractive to entrepreneurs. Although additional research is required to find a reliable and quick procedure for separation of the sexes or techniques for the production of all female populations.