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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 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 Formulation of low fat beef burger with fat replacers(Department of Livestock Products Technology, College of Veterinary and Animal Sciences,Mannuthy, 2010) Govande Premanand, Laxmanrao; KAU; George Oommen, THealth conscious meat consumers prefer low fat meat products due to increasing incidents of high fat induced diseases. Manufacturing meat products with fat replacers (FR) enable to reduce fat and to alleviate the problems with the reduction of fat in products. Therefore, the present study was undertaken with the objectives of developing a palatable and economic formulary for low fat beef burger (LFBB) with carrageenan (CG), tapioca starch (TS), pregelatinised pork skin collagen (PSC) and their blends as FR and to assess its pH, cooking characteristics, proximate composition, nutritional value, textural and organoleptic qualities and shelf life under aerobic (AP) and vacuum packaging (VP) at 0-4oC and -20oC and its cost of production. Beef burgers (BB) are formulated at two different fat levels, viz., full fat (FF) 20 per cent and low fat (LF) 5 per cent as controls. Seven formulations of LFBB with 5 per cent fat are prepared with 0.5 per cent CG, 1.5 per cent TS, 2 per cent PSC and their blends, viz., CG-TS - 0.5% CG & 1.5% TS; CG-PSC - 0.5% CG & 2.0% PSC; TS-PSC - 1.5% TS & 2.0% PSC; CG-TS-PSC - 0.5% CG, 1.5% TS & 2.0% PSC as FR. BB are prepared as per the formularies with minced lean beef trimmings, tallow, salt, spices and condiments, rusk, ice flakes and FR. They are packaged aerobically in HDPE and in vacuum in polyethylene-polyamide (PEPA) pouches. pH, cook yield (CY), cook loss (CL), fat retention percentage (FRP), moisture retention percentage (MRP), dimensional shrinkage (DS), water holding capacity (WHC), Warner-Bratzler Shear Force (WBSF), Hunter L*, a*, b* colour values, proximate and mineral composition and nutritional value, purge loss (PL), Thiobarbituric Acid Reactive Substances (TBARS) value and sensory qualities are assessed on d 0, 10, 20 and 30 of storage at 0-4oC and -20oC or till spoilage, whichever is earlier. Six trials of the experiment were conducted. Cooking reduced the acidity of all the burgers. By the addition of FR a significantly (P< 0.05) very low acid cooked LFBB could be prepared. CY of burgers with CG-TS-PSC was significantly (P< 0.05) the highest with 85.84 per cent. LFBB with blends of FR significantly (P< 0.05) increased CY and correspondingly reduced CL. The DS in LFBB with CG-TS-PSC was significantly (P< 0.05) the lowest with 13.21 per cent. Addition of blends of FR holds water and fat in LFBB and reduces DS during cooking. FRP and MRP in CG-TS-PSC formulation was significantly (P< 0.05) the highest with 97.66 and 74.36 per cent, respectively due to blends of CG, TS and PSC. The WHC of LFBB with CG-TS-PSC was 95.36 per cent and WBSF value 5.30 N comparable to FF and the burgers were significantly (P< 0.05) most succulent, juicy and tender with the addition of blends of FR compared to tougher BB without FR. According to Hunter L*, a*, b* values, LFBB with blends of FR, especially CG-TS-PSC was lighter, less reddish (more bluish) and less yellowish (more greenish) and comparable to FF burger. Fat content in the beef trimmings and PSC were < 1.76 per cent. Cooking significantly (P< 0.05) reduced moisture content with a corresponding increase in the protein, fat, carbohydrate and ash. The percentage total calorific value of LFBB ranged from 6.36 to 7.18 of the Recommended Dietary Allowance (RDA). The contribution of fat to RDA of calorific value was from 2.22 to 2.42 per cent only, which was below the recommended 30 per cent. More than one third of the daily requirement of protein is obtained from 100g of LFBB. LFBB with FR are good sources of Na, K and P but not of Ca. Blends of FR in LFBB, especially CG-TS-PSC, were more efficient in significantly (P< 0.05) reducing PL and TBARS value on storage at 0-4oC for 10 days and at -20oC for 30 days in AP and VP. TBARS values were lower than the acceptable range of 1mg malonaldehyde/kg for oxidative rancidity. The low fat content and the presence of onion containing antioxidants in the formulary would have synergistically acted with CG in reducing the TBARS. On sensory evaluation on zero day, the LFBB with CG-TS-PSC scored significantly higher (P< 0.05) values of 7.00 and above for very good appearance and colour, very intense flavour, very desirable texture, juiciness, practically nil mouth coating and very acceptable overall acceptability similar to FF burger. But saltiness was very desirable than in FF. The LFBB with CG-TS-PSC in AP and VP retained all the sensory attributes and proximate composition even on storage. The very acceptable nature of CG-TS-PSC formulation might be due to the synergistic effect of fat replacers. The LFBB with 5 per cent fat and CG (0.5%), TS (1.5%), PSC (2%) and their blends as FR are developed economically with very acceptable overall acceptability, CY, nutritional quality, reduced PL and oxidative rancidity and shelf life up to 10 days at 0-4oC and 30 days at -20oC under AP and VP. The best LFBB with overall acceptability was CG-TS-PSC followed by CG-TS, CG-PSC, TS-PSC, PSC, CG and TS. Blends of FR are better than single FR, particularly CG-TS-PSC, as they increased CY, FRP, MRP, WHC, sensory attributes and decreased pH, CL, DS, WBSF, PL and TBARS. Further investigations with production of large quantities are required for calculation of cost of production at commercial scale.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 Induction of parturition and evaluation of postpartum fertility in crossbred cows(Department of Animal Reproduction, Gynaecology and Obstetrics, College of Veterinary and Animal Sciences, Mannuthy, 2010) Sheeja, S; KAU; Aravinda Ghosh, K NA preliminary study was conducted by collecting data regarding gestation length and details of calving among crossbred cattle of the University Livestock Farm and local breeds belonging to “ICAR Scheme on Conservation of Germplasm of Vechur Cattle”. The mean gestation length of crossbred cattle of ULF was 274 ± 0.48 days and that of Vechur scheme was 282 ± 0.98 days. The average birth weight of new born calf at ULF was 26.52 ± 0.39 kg and that of Vechur was 10.43 ± 0.12 kg. The sex ratio of male and female was 1: 0.9 and 1: 1.2 for ULF and Vechur scheme respectively The main experiment was undertaken to develop a suitable protocol for induction of parturition in crossbred cattle with prolonged gestation and to assess the postpartum fertility of these animals. The study was performed in 24 pregnant animals of the University Livestock Farm and private farms near by Mannuthy during the period from December 2008 to February 2010. In all animals in group I, II and III, the drug was administered for inducing parturition on 286th day of gestation. In group 1, 24 mg of dexamethsone, in group II 500µg of prostaglandin analogue (cloprostenol) and in group III, a combination of 12 mg of dexamehasone and 250 µg cloprostenol was administered intramuscularly and group IV acted as control. The mean time taken in hours for induction of parturition in group I to III was 39.50 ± 1.26, 30.50 ± 2.17 and 26.90 ± 1.80 respectively and the least time was recorded in combination group. The duration for first stage of labour in groups I to IV was 4.00 ± 0.16, 3.12 ± 0.15, 3.24 ± 0.02, 4.49 ± 0.12 hours respectively and for second stage was 1.27 ± 0.02, 1.12 ± 0.14, 1.21 ± 0.12, 1.53 ± 0.10 hours respectively. The mean time for the expulsion of placenta was 6.67 ± 0.33, 6.35 ± 1.87, 3.02 ± 0.13 2.74 ± 0.14 hours respectively. The mean weight of the placenta for the groups was 2.87 ± 0.43, 3.50 ± 0.54, 3.00 ± 0.28, 3.60 ± 0.25 kg and the mean number of cotyledons were 89.50 ± 0.76, 91.20 ± 0.60, 90.5 ± 0.84, and 91.50 ± 0.76 respectively. The incidence of dystocia in groups I to IV was 50, 0, 33.33 and 50 per cent respectively. The incidence of retention of foetal membranes in groups I to IV was 50, 33.33, 16.66 and 16.66 per cent respectively. In group I, the incidence of postpartum prolapse of genital organs, downer cow and mastitis were recorded as 16.66 per cent each. The sex ratio for the groups I to IV was 1:1, 0.57: 1, 1:1 and 1:1. The mean birth weight in kg for the male calves was 29.33 ± 1.2, 26.65 ±6.5, 31.5 ± 3.40, 34.66 ± 2.03 respectively. Similarly the birth weight of female calves were 30.00 ± 1.15, 27.25 ± 1.97, 23.33 ± 2.40, 32.33 ± 1.20 kg respectively. There was steady increase in body weight of calves as age advanced in experimental and control groups, however there was no significant difference between groups in mean body weight gain. The mean peak yield in the present lactation for the experimental and control animals was 9.57 ± 0.58, 11.33 ±1.17, 11.67 ±1.54 and 13.17± 0.75 liters respectively. The corresponding values in the previous lactation for the experimental and control groups were 11.48 ± 0.48, 11.60 ± 0.75, 12.70 ± 0.47 and 13.50 ± 0.65 liters respectively. The day of peak yield in the present lactation was 25.00 ± 0.63, 21.66 ± 0.61, 22.33 ± 1.05 and 19.16 ± 0.79 days and the corresponding values in previous lactation were 19.80 ± 0.95, 18.70 ± 0.67, 20.30 ± 1.28 and 19.30 ± 0.63 days respectively. The disappearance of lochial discharge for the experimental and control groups was 20.16 ± 1.04, 17.31 ± 1.13, 17.17 ± 0.87, 21.00 ± 1.26 days respectively. The first postpartum oestrus was observed at 33.20 ± 1.25, 30.70 ± 0.88, 29.50 ± 0.76 days for experimental animals and for control animals it was 31.60 ± 0.76 days. Similarly, the second postpartum oestrus was on 59.00 ± 1.22, 51.83 ± 0.83, 48.33 ± 1.99, 53.83 ± 0.94 days respectively. Conception rate for the first AI in group I to IV was 0, 50, 50, and 33.33 respectively where as the overall conception rate for these animals was 16.66, 66.66, 83.33, 66.66 per cent respectively. The highest conception rate was obtained in group III. The mean calving to conception interval for the experimental and control animals was 91.50 ± 15, 77.66 ± 9.38, 74.00 ± 7.00 and 82.00 ± 13.97 days respectively Premature induction of parturition was carried out in four downer cows presented at Veterinary College Hospital, Mannuthy which failed with routine medical treatment and having the gestation length of 253, 285, 270 and 275 days. In the first two animals parturition was induced with prostaglandin and the time taken for induction was 48.30 and 31.20 hours respectively. In dexamethasone treated animal calving occurred at 51 hours after administration of drug. Similarly the time taken for induction in animal which treated with combination of dexamethasone and prostaglandin was 29.45 hours. All the three animals in which prostaglandin and its combination with dexamethasone, recovered from recumbent stage after delivery and had regained normal feeding habits. The animal treated with dexamethasone had not regained the normal condition and was advised disposal. But all the four calves survived in this experiment. The present study revealed that induction of parturition with prostaglandin alone in normal dose and its combination with dexamethasone at a lower dose were equally useful for successful induction of parturition in animals with prolonged gestation with least reproductive complications. When parturition was induced with dexamethasone milk yield was found to be reduced during early stages of lactation while when prostaglandin and its combination with dexamethasone were used reduction in milk yield was negligible. In animals in which parturition was induced with prostaglandin and its combination had normal disappearance of lochial discharge, early involution of uterus and had early normal postpartum oestrus and had fairly good overall conception rate. Further it is recommended that premature induction of parturition in downer cows when all other medical treatments have failed, prostaglandin or its combination with dexamethasone could ideally be used to induce premature induction of parturition to save the life of mother and new born.ThesisItem Open Access Evaluation of wood quality of selected tropical pines raised in the high ranges of Kerala, for pulp and paper making(Department of Tree Physiology and Breeding,College of forestry,Vellanikkara, 2010) Ajayghosh, V; KAU; Anoop, E VA study entitled “Evaluation of wood quality of selected tropical pines raised in the high ranges of Kerala, for pulp and paper making” was conducted in the College of Forestry, Kerala Agricultural University, Vellanikkara, Thrissur during the period 2008-2010. The objective of the study was to evaluate the wood quality of Pinus caribaea Morelet, Pinus patula Schl. et Cham. and Pinus oocarpa Schiede grown in research trials of the Kerala forest department in the high ranges of Idukki district of Kerala. Increment core wood samples were collected at breast height from trees, selected at random, from each plot representing each species belonging to different age levels. These samples were then subjected to intensive investigations to find out radial variation (pith, middle and periphery), species variation and influence of age on different wood physical, anatomical and chemical properties. The study revealed that many of the characters studied were influenced by species and age interaction. Radial variation was also found to have significant difference within the species for characters studied. As a whole, under the present climatic condition P.caribaea was found to perform better with wood properties within the accepted range suitable for pulping and paper making. On the other hand, P. patula and P. oocarpa were also found to be promising species for pulping and papermaking with better derived fiber ratios. However, P. oocarpa had specific gravity value slightly more than that is recommended for pulp and paper making. Studies on chemical composition revealed that P. ooccarpa had better performance with higher cellulose and lower lignin content. So what needs to be determined is the relationship, if any, between wood and tracheid properties of these species and the products which can be manufactured from this renewable resource. For this, more extensive study is needed for which the results of this study could be used as a base line data for future tree improvement aspects of these species with reference to wood quality and to bring out their potential utility for future afforestation programmes and timber utility.ThesisItem Open Access Ultrasonographic evaluation of prostate gland in dogs(Department of Animal Reproduction, Gynaecology and Obstetrics, College of Veterinary and Animal Sciences, Mannuthy, 2010) Divya Nair, R; KAU; Aravinda Ghosh, K NUltrasonographic evaluation of prostate gland of adult male dogs was carried out in the present study to correlate with the fertility of the animal. Initially digital examination of the prostate gland per rectum was performed in 56 male dogs of four different breeds German shepherd, Rottweiler, Dachshund and Spitz to find the location, symmetry, consistency, mobility and pain on palpation. All the dogs were subjected to transabdominal ultrasonographic evaluation of the prostate. Prostatic measurements were taken in longitudinal and transverse sections. In German shepherd dogs of mean age 4.03years and mean body weight 24.21kg, the mean prostatic volume and weight based on formula calculation were 26.62±1.58 and 24.33±1.65 respectively. In Rottweiler, of 3.35 year and 35.25kg, the calculated mean prostatic volume and weight were 26.32±2.55 and 24.01±2.66 respectively. In Dachshund, the mean age was 3.94 years and the mean body weight was 8.71 kg. Calculated mean prostatic volume and weight were 13.07±0.96 and 10.89±0.10 respectively. In Spitz of mean age 2.95 years and mean body weight 5.46 kg, calculated mean prostatic volume and weight were 11.63±0.24 and 8.71±0.25 respectively. In diseased animals, of mean age 6.67 years and mean body weight 20.35kg, calculated mean prostatic volume and weight were 42.73±8.46 and 41.12±8.82 respectively. The measurements were found greater than measurements of adult animals and that suggested prostatic diseases. Four dogs were found having benign prostatic hyperplasia and one with prostatic cyst and another with prostatic abscess. Transrectal ultrasonography was done in German shepherd and Rottweilers and for German shepherd, the mean prostatic length obtained was 2.95±0.10cm and the mean width was 2.44±0.15. For Rottweiler, the mean prostatic length obtained was 2.92±0.15cm and the mean width was 2.42±0.17. Urine and blood were collected from 10 prostatic disease suspected animals and from 10 apparently healthy animals for detailed clinical investigation. Prostatic fluid was collected from them for cytology and culture and sensitivity tests. In disease suspected and normal healthy dogs, urinalysis could not establish major findings except of the presence of few more erythrocytes and squamous epithelial cells in urine of diseased animals. Culture and sensitivity of urine and prostatic fluid were negative in all the dogs. In 40 per cent of the diseased dogs there were presence of neutrophils and in 30 per cent of them, there were few erythrocytes. The mean erythrocyte count obtained for the normal and disease suspected animals were 3.33±1.06 and 3.89±1.41 respectively. The mean leucocyte count obtained for the normal and diseased dogs were 9485.33±1825.95 and 9854± 1921.02 respectively. There was leucocytosis with left shift in one animal. The mean values for Serum alkaline phosphatase in normal and disease suspected dogs were found as 55.53±11.06 units and 62±9.6 respectively. The mean values for serum acid phosphatase in normal and disease suspected dogs were 4.85±1.96 and 4.74±2.10 respectively. From the study, it was found that prostatic disorders mostly BPH were commonly encountered in older dogs without significant change in clinical and biochemical parameters. In conclusion, real- time B- mode ultrasound transabdominal and transrectal scanning was found to be reliable, safe and accurate for the examination of prostate gland in dogs. However, in small breeds, transrectal scanning using a specialised smaller rectal probe will be useful for the evaluation of prostate gland.ThesisItem Open Access Assessment of quality of well water in Eloor, Kerala(Department of Veterinary Public Health,College of Veterinary and Animal Science, Mannuthy, 2010) Divya Rani, Thomas; KAU; Sunil, BA comparative assessment of physical, chemical and microbiological quality of well water from Eloor, an industrial area in Ernakulum District of Kerala, India and Ollukara, a non industrial area, in Thrissur district of Kerala, India, was carried out to correlate the impact of industrialization on quality of well water. A total of 200 well water samples consisting of 100 each from both areas were taken for the study. Of the 100 samples, 25 samples each were collected during four different seasons of the year viz., summer (February), pre-monsoon (March-May), monsoon (June-September) and post-monsoon (October-November), to assess change in the quality of well water with the seasons. Mean temperature of well water was higher in Eloor than in Ollukara. The lowest temperature was recorded during monsoon in Eloor and Ollukara, and the highest temperature was recorded during pre-monsoon in Eloor and summer in Ollukara. Acidic pH was observed in both areas, with significantly lower pH in Ollukara. Higher pH values were observed during monsoon and post monsoon and lower during summer and pre-monsoon seasons. Mean total hardness of water was higher in Eloor than in Ollukara and the difference was highly significant. Highest value of total hardness was observed during summer in Eloor and monsoon in Ollukara. Mean COD of water samples showed no significant difference between two areas. In Eloor, the highest and lowest COD were observed during summer and monsoon, respectively. While in Ollukara, highest and lowest COD were observed during post monsoon and pre monsoon, respectively. Mean nitrate concentration was similar in water samples collected from Eloor and Ollukara with lowest concentration observed during pre - monsoon and summer in Eloor and Ollukara respectively, whereas it was highest during post monsoon in both areas. Mean fluoride concentration in well water samples from Eloor was significantly higher than that of Ollukara and no significant seasonal difference was observed in fluoride concentration in well water from Eloor. However, significant seasonal variations were observed in fluoride concentration in Ollukara viz., lower during monsoon and post monsoon, and higher during summer and pre-monsoon. Mean iron concentration was higher in Eloor and had highly significant difference with mean concentration in Ollukara. Significant difference in mean iron concentrations between four seasons could not be observed in Eloor, whereas in Ollukara, four different seasons showed significant difference. Lower concentration was observed during summer and pre-monsoon and higher during monsoon and post monsoon. A significantly higher lead concentration was recorded in well water from Eloor than that from Ollukara. In Ollukara, there was significant seasonal difference in mean lead concentration with highest during monsoon and the lowest during pre-monsoon seasons respectively. Throughout the entire period of study no mercury could be detected in well water samples from both areas. There was no significant difference in mean zinc concentration between well water samples from Eloor and Ollukara. In Eloor, the concentration in summer season was significantly higher than during other seasons. In Ollukara mean zinc concentration in post monsoon was significantly higher than during other seasons. Mean cadmium concentration was similar in both areas and was found to be significantly higher during monsoon season at both Eloor and Ollukara. It was observed that mean Aerobic Plate Count was higher in Eloor than that of Ollukara and the difference was highly significant. There was no significant difference observed between four seasons in Eloor. In Ollukara, significant difference between seasons could be observed with highest count during summer. The mean coliform count of well water from Eloor was significantly higher than that of Ollukara. There was no seasonal variation in mean coliform count in Eloor. Whereas significant variation in mean colifrom count between seasons was observed in Ollukara with highest count during monsoon and lowest during summer. The mean E. coli count in well water from Eloor and Ollukara did not differ significantly. There was no difference in mean E. coli count between four seasons in well water from Eloor and Ollukara. The mean enterococcal count of well water samples from Eloor and Ollukara did not show significant difference. The mean count was significantly higher in Eloor during summer, but there was no seasonal difference in enterococcal count in Ollukara. From the survey conducted among 25 households having wells in Eloor and Ollukara, it could be concluded that 20 and 100 per cent of households, used well as source of drinking water in Eloor and Ollukara respectively. Eighty percent wells were pucca wells in Eloor, whereas only 60 per cent of wells were pucca in Ollukara. Disinfection of wells was practiced by 48 and 52 per cent respectively in Eloor and Ollukara. Only 32 and 36 per cent wells respectively had distance more than 15 metre from nearest polluting source. Among the major human health problems in Eloor, 88, 72, 60, 40, 12, 4 and 16 per cent of household reported respiratory problems, skin diseases, musculoskeletal diseases, headache, ophthalmic problem, neoplasm and congenital anomalies and mental retardation, respectively, which were suggestive of iron, lead and cadmium toxicity and poor quality of air. Whereas in Ollukara, health problems were comparatively less and only 12 per cent house hold reported respiratory problem. Among the major animal health problems in Eloor were digestive disorders, reproductive disorders, skin diseases and lameness indicating iron, lead, cadmium and fluoride toxicity. Retrospective analysis of cases recorded in Eloor veterinary hospital, from January 2005 to December 2009, also revealed symptoms of iron, lead and cadmium toxicity in animals. It was observed that Kuzhikandam creek in Eloor was heavily polluted and acted as a potent source of groundwater pollution. From the comparative study, it was clear that the groundwater contamination in Eloor was purely chemical of industrial origin, while in Ollukara it was attributed to the soil type and household pollution. Construction of sanitary wells, keeping adequate distance from polluting sources, with adequate platform, drainage and parapet is recommended. Steining of wells and covering the wells with nets should also be adopted. Disinfection of wells with sufficient quantity of suitable disinfectant at regular interval also helps to minimize pollution mainly of microbial origin.ThesisItem Open Access In vitro maturation of caprine follicular oocytes(Department of Animal Reproduction, Gynaecology and Obstetrics, College of Veterinary and Animal Sciences, Mannuthy, 2010) Ambili, John; KAU; Joseph, MathewThis study was designed to analyse the effect of three oocyte retrieval methods, aspiration, slicing and puncture on the yield of different quality grades of oocytes and to evaluate the in vitro maturation rate of different grades of caprine oocytes. One hundred and thirty eight ovaries of Malabari goats and its crossbreds collected from the slaughter house were subjected to the oocyte retrieval methods. The oocytes harvested were graded based on the number of cumulus cell layers and ooplasm character into A, B, C and poor quality grades. Oocytes of A, B and C grades were subjected to maturation for 24 h in TCM-199 medium under standard culture conditions. Average yield of COC per ovary by aspiration, slicing and puncture was 3.93 ± 0.11, 4.44 ± 0.06 and 3.59 ± 0.07 respectively. Yield was significantly higher in slicing method than aspiration and puncture. The percentage yield of A, B, C and poor quality grades of oocytes by aspiration method was 26.74 per cent, 26.62 per cent, 24.77 per cent and 21.87 per cent respectively. Mean yield of oocytes of each quality grade by the same method were 1.05 ± 0.05, 1.05 ± 0.08, 0.98 ± 0.07 and 0.86 ± 0.04 respectively. Slicing yielded 23.08 per cent A class, 28.15 per cent B class, 24.44 per cent C class and 23.96 per cent poor quality oocytes. Mean yield of oocytes per ovary in these classes by slicing method were 1.04 ± 0.04, 1.25 ± 0.05, 1.08 ± 0.07 and 1.06 ± 0.06 respectively. Percentage yield of A, B, C and poor quality oocytes by puncture was 29.01 per cent, 30.26 per cent, 22.07 per cent and 18.66 per cent respectively. Mean yield per ovary by puncture method was 1.04 ± 0.04, 1.08 ± 0.03, 0.79 ± 0.04 and 0.67 ± 0.03 for A, B, C and poor quality oocytes respectively. No significant difference was observed in the yield of A, B and C class oocytes between aspiration, slicing and puncture. Yield of poor quality oocytes were significantly more in slicing method. The cumulus expansion rate of A class oocytes obtained by aspiration, slicing and puncture was 77.75 per cent, 69.70 per cent and 71.49 per cent respectively. Class C oocytes exhibited a cumulus expansion rate of 63.48 per cent, 51.37 per cent and 63.39 per cent respectively when collected by aspiration, slicing and puncture method. Class C oocytes obtained by aspiration, slicing and puncture when subjected to in vitro maturation exhibited a cumulus expansion rate of 39.17, 32.57 and 37.29 per cent respectively. Retrieval method was found to have no significant effect on cumulus expansion potential of caprine oocytes, whereas the COC morphology had significant effect on cumulus expansion potential. Nuclear maturation rate of A class oocytes collected by aspiration, slicing and puncture method were respectively 40, 30 and 50 per cent and polar body extrusion rate was 30, 20 and 30 per cent respectively. Class B oocytes exhibited nuclear maturation rate of 20, 10 and 30 per cent and polar body extrusion rate of 10, 10 and 20 per cent respectively by aspiration, slicing and puncture. Ten, 10 and 20 per cent of C class oocytes retrieved by aspiration, slicing and puncture exhibited nuclear maturation and 10 per cent polar body extrusion was observed in C class oocytes retrieved by puncture. None of the C class oocytes collected by aspiration or slicing exhibited polar body extrusion. This study proved that slicing is a better method than aspiration or puncture for retrieval of oocytes from caprine ovaries as it yielded more number of oocytes per ovary. Retrieval methods had no significant effect, whereas COC morphology was found to have significant effect on cumulus expansion, nuclear maturation and polar body extrusion rates of different grades of oocytesThesisItem 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.
