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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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1991 - 19933
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Subject: Floriculture and Landscaping × End date: 1993 × Start date: 1990 × Type: Thesis ×
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    ThesisItemOpen Access
    Evaluation of f 1 hybrids resistant to bacterial wilt and inheritance of resistance in brinjal (lolanum melongena L.)
    (Department of Olericulture, College of Horticulture, Vellanikkara, 1991) Geetha, Varghese; Abdul, Vahab M.
    The present studies "Evaluation of F hybrids resistant to bacterial wilt and inheritance of resistance in brinjal ( Solanum melongena L . ) were conducted during February 1990 to July 1991in the vegetable research plots of Kerala Agricultural University,Vellanikkara. Evaluation of F hybrids over 4 environments revealed that all the 3 hybr ids were superior to their parents for yield during all the four seasons. It also indicated significant role of genotype x environment interaction in the yielding abi l ity of the hybrids. Considering wilt resistance the hybrids were not superior to their parents. Varietal difference was observed for plant height, fruits/plant, fruit weight, fruiting period and productive flowers. Estimation of heterosis of three F^s over their parents revealed significant heterosis for plant height, days to flower, days to first fruitset, days to harvest, primary branches/plant, total fruits/plant, total yield/plant, average fruit weight and fruiting period. All the three hybr ids viz. Surya x Pant Rituraj, SM 6-6 x SM 132, SM 6-2 x Pusa Purple Cluster were stable. Study on the nature of inheritance showed that resistance to bacterial wilt is inherited in a recessive and monogenic manner.
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    ThesisItemOpen Access
    Effect of time of planting and growth regulators on flowering and vase life of Gerbera jamesonii
    (Department of Pomology and floriculture and Landscaping, College of Horticulture,Vellanikara, 1993) Suma, P; KAU; Lila Mathew, K
    Studies were carried out in the Department of pomology and Floriculture, College of Horticulture, Vellanikkara, Thrissur, during 1991 – 93 to examine the effect of time of planting and growth regulators on flowering and vase life of gerbera. Four varieties, namely , Eoliet, Presley, Pritty and Sunbird and five treatments, viz., GA 50 ppm, GA 100 ppm, CCC 500 ppm, CCC 750 ppm and control, were tried. Varieties were found to have significant influence on both vegetative as well as the floral characters whereas the treatments did not have any significant effect on vegetative characters of the Gerbera cultivars in general, when evaluated in the first season. In the second season both varietal and treatment effects were not consistent. Variety Presley was found to be early flowering while Eoliet was late flowering. GA 50 ppm and GA 100 ppm hastened flowering whereas CCC 500 ppm and CCC 750 ppm delayed it. In general the longevity of flowers was maximum in varieties Eoliet and Sunbird. Variety Presley had the least longevity. Among the treatments, CCC 750 ppm and GA 50 ppm increased the longevity of flowers in field. Maximum number of blooms was produce by Presley and the minimum by Eoliet. In general GA 100 ppm and CCC 750 ppm increased the number of blooms. In general CCC 750 ppm, GA 50 ppm and GA 100 ppm had a significant positive influence on flower diameter. In general variety sunbird had the maximum stalk length and diameter, while Pritty produced the shorest stalks. CCC 500 ppm and CCC 750 ppm had the best effect on stalk length. Vase life was found to be significantly increased by GA 100 ppm and CCC 750 ppm treatments given to the plants. Five per cent sucrose + 20 ppm AgNO3 significantly increased the longevity of flowers in vase. Planting in June was found to be better than October planting with respect to vegetative as well as floral characters, especially for number of flowers and flower diameter. Among the varieties, with respect to growth and number of flowers, Presley was found to be superior. In the correlation studies flower number was found to have positive and highly significant correlation with plant height and leaf area whereas flower diameter had significant negative correlation with leaf area and stalk length. Petiole length, stalk diameter and leaf number had positive correlation with this character. Vase life had significantly positive correlation with fresh weight of flowers.
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    ThesisItemOpen Access
    Induction of Genetic Variability in Musa Sp. Var. Nendran By in Uitro Methods
    (Department of pomology and floriculture, College of horticulture,Vellanikkara, 1993) Mini Balachandran; P.K.Valsalakumari
    Investigations were carried out at the Department of Pomology and Floriculture and Plant Tissue Culture Laboratory of the All India Co-ordinated Floriculture Improvement Project, College of Horticulture, Vellanikkara, Thrissur, during 1991-93 on the induction of variability in the banana variety Nendran (Musa AAB ‘Nendran’) by in vitro methods. Explants utilized for the study were shoot tip and eye bud for direct organogenesis through enhanced release of axillary buds and shoot tip, flower base, inflorescence axis, embryonic leaves and scalp for somatic organogenesis/embryogenesis. For culture establishment, axillary shoot initiation and in vitro rooting, different growth regulators, like NAA, 2, 4-D and 2, 4, 5-T (auxins) and BA and kinetin (cytokinins) were made use of. The plantlets produced in vitro were subjected to hardening treatments to ensure a better establishment of planted out plants and their growth parameters were studied. For shoot tip and eye bud explants, a combination of treatments involving, an initial dipping of explants in emisan (0.1 per cent) for 30 minutes followed by dipping in norfloxacin (0.1 per cent) for 30 minutes followed by dipping in norfloxacin (0.1 per cent) for 30 minutes and finally rinsing the explants in mercuric chloride (0.1 per cent) for 20 minutes was found to be best, but for flower base and inflorescence axis explants, emisan (0.1 per cent) treatment for 20 minutes and for embryonic leaves, dipping in alcohol for one second were in the best. Better and speedier establishment and growth of shoot tip and eye bud explants were observed on MS (semi-solid) medium containing NAA 2 ppm + BA 5 ppm. Addition of activated charcoal (500 mg per litre) to the medium, reduced media and explant discolouration due to polyphenol oxidation. When the performance of the shoot tip and eye bud explants was compared, eye bud explants took more time for culture establishment and growth. In shoot tip culture, on an average, each explant released 8.66 axillary shoots in the treatment involving MSb*+ NAA 2 ppm + BA 10 ppm. In the case eye bud, on an average, each explant released five axillary shoots. Continuous sub culturing was carried out at two week interval to assess the variation induced to cultured plants due to repeated subculturing. It was found that, the number of shoots produced per culture was not constant in all the subcultures. Still, the axillary shoots produced per explant per culture vessel increased at the mean rate of 5.90. BA alone at higher concentration (10 ppm) resulted in colloid (globular semi-hard, light green callus like structure) formation and subsequent regeneration. MSb*: MS medium containing half concentration of inorganic salts and full concentration of organic growth factors. For in vitro rooting, MSb medium containing NAA 10 ppm and AC 0.05 per cent was found to be effective for early root initiation and the maximum number of roots per shoot was produced at the treatment involving MSa* +NAA 5 PPM+ AC 0.05 per cent. Of the various explants, viz., shoot tip, inflorescence axis, flower base, embryonic leaves and scalp(in vitro) tried for initiating collus scalp and embryonic leaves recorded maximum response. Among the media tried for callus initiation, MSb media at liquid consistency was found to be more effective. Maximum callus index (266) was recorded for the treatment combination involving 2, 4-D 7 ppm and BA I ppm. For callus differentiation the treatments involving 2, 4-D and BA, BA alone and basal MS media resulted in rhizogenesis, and treatments involving 2, 4-D alone produced embryoid like structures from scalp callus. No shoot organogenesis was observed. Also treatments were conducted with changed levels of nitrate source in the media, but they did not give any favourable results. Embryoid like bipolar structures were recovered from scalp callus when they were transferred to media devoid of growth regulators. To study the variation, if any, induced due to derail subculturing, the shoots obtained from each subculture cycle (through enhanced release of axillary buds) were isolated and their MSa* : MS medium containing full concentration of inorganic salts and organic growth factors identify maintained. The shoots thus separated were rooted and planted out after subjecting them to a process of hardening. Somatic chromosome counts were made at the root tips of plantlets from 10 subcultures to confirm the ploidy. All the plants were triploids (2n = 33). The plantlets from different subcultures were planted out in sand, which was found to be the best medium. Observations made on growth parameters, at fifteen days interval, revealed that the plants from subcultures differed significantly with respect to the rate of growth in height and leaf area.