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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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    ThesisItemOpen Access
    Effect of planting date, weight of rhizome and spacing on the growth, yield and quality constituents on turmeric (Curcuma longa L)
    (Department of Horticulture (Plantation Crops & Spices), College of Horticulture, Vellanikkara, 1983) Chatterjee, R K; KAU; Mohanakumaran, N
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    Institutional PublicationsItemOpen Access
    Water resources developemt in KAU : present conditions and future possibilities
    (Kerala Agricultural University, Vellanikkara, 1983) KAU
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    Institutional PublicationsItemOpen Access
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    Institutional PublicationsItemOpen Access
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    Institutional PublicationsItemOpen Access
    Development plan (Sixth plan period) 1978-79 to 1982-83
    (Kerala Agricultural University, Vellanikkara, 1983) KAU
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    Institutional PublicationsItemOpen Access
    Summary report 1982-83
    (Kerala Agricultural University, Vellanikkara, 1983) KAU
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    ThesisItemOpen Access
    Economics of banana cultivation in Trichur district
    (Department of Agricultural Economics, College of Horticulture, Vellanikkara, 1983) Indira Devi, P; KAU; Mukandan, K
    This investigation on economics of banana cultivation in Trichur district was conducted during 1983.The study confined to irrigated nendran banana in Chalakudy block with the following objectives viz. to estimate cost and returns; to evaluate resource use efficiency in production; and to study the problems of banana growers. Ninetyeight holdings were selected by following the stratified two stage random sampling technique and the information was collected using a pretested schedule, through personal interview. The total cost of cultivation (cost C) of banana worked out to Rs.41814.13 per hectare. Of this, the most important item of expenditure was human labour. Average labour requirement for banana cultivation was 702.96 mandays per hectare. This was followed by expenditure on manures, fertilizers, propping materials, suckers and irrigation. All of the farmers in the locality applied chemical fertilizers though not upto the recommened level. Plant protection expenses were only 0.30 per cent of total cost. In the operationwise expenditure, manures and manuring operations demanded highest investment and formed 42.50 per cent of total cost. Propping, planting, after cultivation and irrigation, harvesting and handling and preparatory cultivation in that order were the other operations which needed investment. Plant protection operations accounted for 0.92 per cent of total cost. The average returns from banana cultivation were Rs.65011.90 per hectare. The net income from banana cultivation was Rs.23,197.77 per hectare with a benefit cost ratio of 1.55. On a per plant basis, the average cost of producing a bunch was Rs.14.31 and it gave a return of Rs.26. In the linear production function model fitted, plant population and expenditure on labour were the factors which had significant influence on the dependent variable viz. total returns. The former had a positive influence and for the latter the influence was negative. The same model was fitted for the data converted to a per plant basis. The analysis revealed that the farmers were using labour over and above the optimum level. So its use has to be restricted.
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    ThesisItemOpen Access
    Effect of growth regulators and certain formulations on bunch development in banana var. palayankodan
    (Department of Pomology & Floriculture and Landscaping, College of Horticulture, Vellanikkara, 1983) Rajendran, P; KAU; Aravindakshan, M
    The yield of banana in Kerala remains very low inspite of the adoption of proper manuring and other management practices. Investigations have indicated that the main barrier to the increased production in banana is the lack of sufficient leaf area at the active phase of growth of the plants. The present experiment was conducted with the banana cultivar ‘Palayankodan’ under sparsely irrigated conditions with a view to increase the plant growth and ultimate yield by the use of growth regulators and commercially available formulations. The growth regulators viz., 2-4-D and NAA and the commercially available formulation namely ‘Navras Banana Special’ were tried at four different concentrations as given below:- 2,4-D - 5,10,15 and 20 ppm NAA - 20, 30,40 and 50 ppm ‘Navras’ - 0.25, 0.50,0.75 and 1.00 per cent The various chemicals at different concentrations were applied as two foliar sprays at three and four months after planting. A third spray was also given on the bunches immediately after the female phase of flower opening. On an overall analysis, 2,4-D at 20 ppm and ‘Navras’ at 0.50 per cent were found to be more effective in promoting the vegetative growth of plants. With respect to flowering and duration of the crop, the growth regulators alone had significant effects when compared to the commercial preparation ‘Navras’. The effectiveness also depended on the concentrations of the growth regulators. Thus 2,4-D at 20 ppm induced early shooting of plants by about 12 days whereas NAA at 50 ppm caused substantial delay in shooting. The chemicals at their various concentrations were not effective in influencing the bunch maturity, thus indicating that the applied chemicals caused the earliness or delay observed, through their influencedon the vegetative growth only. Consequent to the application of 2,4-D at 20 ppm the crop duration was advanced by 22 days. Contrary to this, NAA at 50 ppm delayed the duration of the crop. The treatments with 2,4-D at 5 to 20 ppm, NAA at 40 and 50 ppm and ‘Navras’ at 1.00 per cent were found to advance the ripening of fruits. The best quality fruits in terms of TSS and total sugars were obtained by the application of 2,4-D at 20 ppm. Among the concentrations of ‘Navras Banana Special’, o.5 per cent gave the best results with respect to the growth and yield of plants. When the concentration was increased further, there was a decrease in the performance of the plants. The optimum doze of ‘Narvas Banana Special’ was worked out to 0.534 per cent. The correlations worked out from the data collected revealed that the vegetative and bunch characters such as girth of psuedostem, number of functional leaves, total leaf area, length of bunch, number of hands and fingers per bunch, number of fingers per hand and weight of hand, length, girth and weight of fingers amply contributed to the overall yield in the form of bunch weight. The yield increase observed in the present study due to the application of 2,4-D at 20 ppm was by 88 per cent and that for ‘Navras’ at 0.5 per cent was by 96 per cent. The benefit/cost ratio worked out for these treatments did not differ and hence application of 2,4-D (20 ppm) and ‘Navras Banana Special’ (0.5 per cent) were equally good for increasing the yield. The present investigations were conducted under sparsely irrigated conditions where, irrigation was given just for the maintence of the crop. Further investigations with rainfed and irrigated ‘Palayankodan’ bananas may be of particular interest.
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    ThesisItemOpen Access
    Ochratoxicosis in the goat
    (Department of Pathology, College of Veterinary and Animal Sciences, Mannuthy, 1983) Maryamma, K I; KAU; Krishnan Nair, M
    An experimental study was carried out to delineate the pathological effects of ochratoxin in goats. A comparative assessment of ochratoxin production by A. ochraceus and A. sulphureus on what and rice under static and shake cultures was also made. A. ochraceus was found to be a better toxin producing strain in both substrates under static and shake cultures systems and wheat was a better substrate than rice. Toxicity studies were conducted in Sannen – Malabari cross-bred goats of 1 to 3 months age. Purified ochratoxin produced in the laboratory was administered by oral, intra-peritoneal and intravenous routes. The different dose levels adopted were 2.5 mg/kg body weight, 1 mg/kg body weight and 0.5 mg/kg body weight. The synergistic effect of ochratoxin and aflatoxin in goats was studied by adminstering the crystalline toxins simultaneously (Makor Chemicals, Israel) by itraperitoneal route. The parameters of study were: clinical signs, haematological and biochemical alterations, pathological changes in urine, and macroscopic, microscopic and ultra-structural alterations in organs. Varying degree of clinocopathological changes were noticed in the test animals. The animals became weak and listless and in general there was reduction of total erythrocyte count, PCV, haemoglobin and lymphocyte count. Serum protein level was lowered while BUN and creatinine and blood coagulation time were high. There was rise in ALP, SGOT and SGPT in some of the test animals. The changes and degree of variation depended on the dose, total quantity and rate of administration of the toxin and duration of the experiment. More severe alterations were noticed when ochratoxin and aflatoxin were administered simultaneously. Important changes in the urine were lowering of pH, albuminurea and presence of epithelial cells and casts. Pathological changes varied in severity in different organs and were observed in the following descending order: kidney, liver, intestines, stomach, lymph nodes, spleen, thymus, genital organs, endocrines. In the kidneys, the order of intensity of pathological alterations was: proximal convoluted tubules, Henle’s loop, distal convoluted tubule, glomeruli, collecting tubules. Retrogressive changes of different degree and necrosis of the lining epithelial cells of tubules and endothelium and epithelium of glomeruli were the important lesions. Changes in glomeruli and Bowman’s capsule noticed in the higher dose group included shrinkage of glomeruli and presence of proteinaceous material in the capsular space. Eosinophilic granular casts and PAS positive bodies were present in the lumen of tubules. The necrobiotic renal changes were more intense when orchatoxin and aflatoxin were administered simultaneously. Hepatic lesions were mainly fatty infiltration, necrosis of hepatocytes and haemorrhage. The changes were most severe in combined toxicity. Mallory bodies and mild biliary hyperplasia were noticed in a few sections. Necrosis and subsequent depletion of lymphocytes wee the lesions in lymph nodes, spleen and thymus in some test animals. Degenerative changes were also noticed in testis, ovary, pituitary, adrenals and pancreas in experimental groups. In the combined toxicity group the pathological effect was more intense. At the ultra-structural level, the hepatcytes as well as the epithelial cells in the kidney showed severe changes. The cell organelles were either completely damaged or showed partial configurational alterations. Mitochondria showed changed in the density of matrix as well as disorientation and destruction of the limiting membranes and cristae. Cytolysosomes incorporating damaged cell organelles were abundant. Disaggregation of ribosomes and fragmentation of ER were noticed. In the glomerulus, there was destruction of the basement membrane and disruption of the regular arrangement of the foot processes of podocytes. In the cytoplasm of hepatocytes, Mallory bodies and lipid droplets were present. Varying degree of nuclear changes like clumping, condensation and disappearance of chromatin and fragmentation of nucleolus and nuclear membrane were observed. Changes occurred in the tight junctions of epithelial cells of bile ducts. Pathological alterations were more pronounced when ochratoxin was administered by the pwerenteral route. Oral administration of toxin also effected structural alterations which indicated that some fraction of ochratoxin escaped degradation in the rumen. From this study it became evident that aflatoxin potentiated the effect of ochratoxin. The structural damage to the cells might be due to the inhibition of oxidative enzymes which is reflected by the extensive ultra- structural alteration observed in the mitochondria and RER. Biochemical changes like high BUN and creatinine were evidently due to necrobiotic changes in the kidney. Interference in the synthesis of proteins due to damage of hepatic cells and escape of protein molecules due to alteration in the podocyte foot processes and basement membranes may account for the reduced serum protein levels. The nature of organellar destruction and configurational changes in the cells indicate the toxic potency of the mycotoxin on the biological system.