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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 Influence of different levels of energy on growth performance of crossbred pigs(Department of Animal Nutrition, College of Veterinary and Animal Sciences, Mannuthy, 2001) Rekha, P; KAU; George, MathenAn experiment was conducted to assess •the influence of different levels of energy on the growth performance of crossbred (Large White Yorkshire x Desi) pigs. Fifteen male (castrated) and fifteen female weaned crossbred piglets with an average body weight of 12.9 kg were divided into three equal groups as uniformly as possible with regard to age, sex and body weight. The three groups of piglets were maintained on three rations with 16 per cent crude protein but differing in their energy content, viz., 2800 kcal (T1), 3000 kcal CT2) and 3200 kcal (TI) of digestible energy (DE) per kg. The average daily gains recorded for the three groups T1, T2 and TI were 262.9, 302.0 and 362.8 g respectively. The cumulative feed conversion efficiencies were 6.0, 5.2 and 4.1 for the groups T1, T2 and TI respectively. The values recorded for TI were higher (P<0.01) than those for T1 and T2. The digestibility coefficients of nutrients except that of crude fibre and crude protein were found to improve with increase in the energy content of the rations. Study of the carcass traits revealed that the body weight at slaughter and dressed weight without head improved as the energy content of the rations increased. However, dressing percentage, carcass length and back fat thickness were not significantly influenced by the energy content of the ration. The cost of feed per kg weight gain of animals was significantly lower (P<0.01) for the dietary treatment T3 compared to that of T2 and Tl, the values being Rs.49.90, 43.30 and 34.10 for Tl, T2 and T3 respectively. The above results indicate that crossbred pigs require 3200 kcal of DE/kg of the ration for better growth performance provided the crude protein level is maintained at 16 per cent.ThesisItem Open Access Investigations on etio-pathology of vomiting in dogs(Department of Clinical Medicine, College of Veterinary and Animal Sciences, Mannuthy, 2001) Muraly, P; KAU; Baby, P GThe study "INVESTIGATIONS ON ETIO-PATHOLOGY OF VOMITING IN DOGS" was conducted in 20 dogs to evaluate ultrasonography and radiography as diagnostic tools in vomiting dogs; to assess hydration status, electrolyte and acid-base balance in vomiting dogs and to correlate clinico-pathologic findings with radiographic and ultrasonographic changes. Various parameters such as history, physical examination, hydration status, ultrasonography, radiography-plain and contrast, haematology, serum biochemistry, and wherever possible histopathology were studied. Most of the dogs under study had bile stained watery vomitus but dogs with pyloric stenosis had frothy or watery white vomitus. The frequency of vomiting in dogs with gastritis and gastrointestinal (GI) obstruction was two to seven times per day, it was variable in dogs with hepatic and renal disorders, but was associated with food intake in dogs with pyloric stenosis. Physical examination was found useful in dogs with GI obstruction, while it was non-specific in dogs with gastritis and renal disorders. Capillary refill time (CRT) and degree of sunken eye balls were helpful to assess dehydration. Estimation of volume of packed red cells (VPRC) was found beneficial to assess dehydration unless the dogs are anemic. Ultrasonography could not identify any lesions in dogs with gastritis, but was useful to detect GI obstructions due to pyloric stenosis, intussusception and foreign body and to characterise lesions in the parenchymal organs like liver and kidney. While plain radiographs could give indication to possible non-radiopaque GI obstructions, contrast radiography was required to confirm. Radiography could not identify any lesions in dogs with gastritis, hepatic and chronic intestitial nephritis. Hypokalemia with metabolic alkalosis was the significant electrolyte and acid-base derangement in dogs with vomiting due to gastritis and GI obstructions.ThesisItem Open Access Immunodiagnosis of bovine gastrothylacosis using coproantigens(Department of parasitology, College of Veterinary and Animal Sciences, Mannuthy, 2000) Kandasamy, A; KAU; Devada, KA study was conducted on the prevalence of paramphistomatidosis in Thrissur from June 1999 to May 2000, feasibility of coproantigen detection by ELlSA and comparison of sensitivity of ELlSA using coproantigens and ELlSA using serum antibodies in diagnosis of gastrothylacosis, caused by Gastrothy/ax crumenifer, in cattle. It was noted from the registers maintained at the University Veterinary Hospitals at Kokkalai and Mannuthy and that at the Department of Veterinary Parasitology, College of Veterinary and Animal Sciences, Mannuthy, that out of a total number of 1534 faecal samples from bovines examined, 253 (16.5 per cent) animals were found to be positive for amphistome eggs with the maximum prevalence (23 per cent) in June and July. Generally the infection was prevalent throughout the year. An indirect ELlSA using rabbit hyperimmune serum against somatic antigens of G. crumenifer was performed to detect coproantigens in faecal samples collected from 100 known G. crumenifer infected cattle. Seventy four samples were found to contain detectable levels of coproantigen indicating a sensitivity of 74 per cent. Serum samples collected from the same infected cattle were tested for antibodies to G. crumenifer by an indirect ELlSA using somatic antigens. Fifty one samples were found positive for antibodies indicating a sensitivity of 51 per cent. It was seen that when 43 cattle were positive for both coproantigens and serum antibodies, 18 cattle were negative for both of them. Although 31 cattle which were negative for serum antibodies were found positive for coproantigens, eight cattle negative for coproantigens were found positive for serum antibodies. The results showed that coproantigen detection, which revealed a higher sensitivity than the detection of serum antibodies by ELlSA, is feasible for the diagnosis of gastrothylacosis in bovines.ThesisItem Open Access Effect of processing and freezing procedures on the acrosome morphology of buck spermatozoa(Department of Animal Reproduction, College of Veterinary and Animal Sciences, Mannuthy, 1998) Ranjini, A; KAU; Prabhakaran Nair, KSix pooled semen samples (two ejaculates) of good quality from five Malabari crossbred bucks were processed and frozen in two different protocols to evaluate the effect of processing and freezing procedures on the acrosome morphology of buck spermatozoa. In protocol I, the samples were diluted 10 fold in Tris buffer before centrifuging twice and the final pellet was re-suspended in the non glycerolated fraction of Tris yolk diluent. The sample was glycerolated (six per cent), equilibrated (four hours), frozen (eight minutes), and thawed (250 C for 30 seconds). In protocol 11, centrifugation was done only once, after 15 fold dilution in Tris buffer. The re suspended pellet was glycerolated (seven per cent), equilibrated (three hours), frozen (10 minutes) and thawed (60° C for 10 seconds). The semen characters such as motility, live sperm, sperm abnormalities and acrosome abnormalities were evaluated at the end of washing and initial extension (stage I), cooling to 5° C (stage II), glycerolisation and equilibration (stage Ill) and freezing and thawing (stage IV). The results were compiled to evaluate the effect of different processing and freezing procedures on the semen characters in general and acrosome morphology in particular. The semen sample used for split sample dilution had a mean volume of 1.3282± 0.067 ml, creamy in colour, DDDD density, ++++ mass activity, pH of 7.275 2± 0.040 and a concentration of 2972 2± 293 millions per ml. No significant difference in the above semen characters were found between bucks. The initial sperm motility of 82.000 2± 0.606 was found to drop significantly during processing and freezing and the final post thaw motility obtained was 44.000 2± 0.790 in protocol I. Similarly in protocol II the initial motility dropped from 81.375 2± 1.089 to 44.750 2± 1.075 at the end of stage IV. Even though there was significant drop in motility between stages in both the protocols, there was no significant difference in the corresponding stages of the two protocols. It could be inferred that good post thaw motility was obtained in both the protocols. The fact that a single washing and centrifugation was only adopted in protocol II makes it a more acceptable procedure for buck semen freezing. The mean live sperm percentage of fresh semen was evaluated using both NE and NEG staining technique. The percentage of live sperms of 90.050 2± 0.801 was found to decrease to 54.250 2± 0.593 after freezing and thawing in protocol by NE staining. Similarly in protocol 11, the mean percentage of live sperms was found to reduce to 53.125 2± 0.793 with the same staining. Even though there was significant difference in the live sperm percentage between stages within protocol I and II no significant difference in the live sperm percentage between the corresponding stages of protocol I and I I . With NEG staining the initial live sperm percentage of 80.850 ± 1.494 was found to drop to 54.875 ± 0.677 in protocol I as against 53.400 ± 0.730 in protocol II. While there was significant difference in the live sperm percentage between stages within protocol I and II there was no variation between corresponding stages of the two protocols. A significantly lower percentage of live sperms was recorded with NEG staining when compared with NE staining probably on account of the fact that the differentiation of live and dead sperm was difficult in the former staining method as live sperms were stained light blue instead of colourless. The mean percentage of abnormal sperms of 3.050 ± 0.245 in fresh semen did not register any significant increase during processing. However, there was significant increase in the percentage of sperm abnormalities during freezing and thawing with the final abnormality percentage of 7.125± 0.706 in protocol I and 6.300± 0.36 in protocol II. The initial acrosomal abnormality of 8.825 in the fresh semen steadily rose to 23.375 in protocol I as against 19.825 in protocol II at the end of stage IV. There was no significant difference in the percentage of various acrosomal abnormalities between corresponding stages of the two protocols. However, there was significant increase in the acrosomal abnormalities during glycerolisation, equilibration, freezing and thawing under both the protocols. It was concluded that the processing and freezing under two different protocols did not significantly alter the post thaw motility, percentage abnormal and dead sperms and acrosomal abnormalities. A good post thaw motility and low acrosomal abnormality was obtained with a single washing of buck semen with 15 fold Tris buffer which was comparable with double washing with 10 fold Tris buffer.ThesisItem Open Access Effect of probiotic supplementation on the performance of broiler chicken(Department of Poultry Science, College of Veterinary and Animal Sciences, Mannuthy, 2001) Sabitha Mahaboob Kadari, A; KAU; Elizabeth, V KThe effects of different levels of pro biotic (Lactobacillus acidophilus, Streptococcus faecium and Yeasacc 1026) supplementation• at 0.025 and 0.05 per cent of the ration on the performance of broiler chicken were evaluated using 144, one-day old, commercial broiler chicks for a period of eight weeks. The birds were divided into three dietary treatment groups viz., standard broiler ration (T 1), standard broiler ration with 0.025 per cent probiotic (T 2) and standard broiler ration with 0.05 per cent probiotic (T3). Standard broiler ration was formulated as per Bureau of Indian Standards (1992) specification for broiler chicken feed. The 0.025 per cent probiotic supplemented birds showed a significantly higher (P<0.05) body weight upto six weeks of age. At the end of eight weeks of age, the 0.05 per cent probiotic fed birds grew faster. The body weight gain was significantly higher in 0.025 per cent probiotic supplemented group upto six weeks of age but was statistically non-significant upto eight weeks of age. The feed intake was not statistically significant throughout the experimental period. Eventhough the feed efficiency was significantly (P<0.01) better in the group fed with 0.025 per cent probiotic at the end of second week, it was statistically non-significant at sixth and eighth weeks of age. The protein efficiency was not significantly different throughout the experimental period. The serum cholesterol levels were significantly (P<0.01) reduced in both the probiotic supplemented groups. The serum protein level was not affected by probiotic supplementation. The processing Yields did not show any significant difference among treatments. The mortality percentage was not affected by treatments. Cost of production of broilers in the 0.025 per cent probiotic group was lower when compared with other two groups at the end of six weeks of age, while it was lower in the 0.05 per cent probiotic supplemented group at the end of eight weeks of age. It can be concluded that probiotic supplementation in standard broiler ration at a lower level was beneficial in the early stages of growth.ThesisItem Open Access Assessment Of Bacteriological quality Of Raw Milk In Trichur And Its Public Health Importance(Department of Veterinary Public Health, College of Veterinary and Animal Sciences,Mannuthy, 1995) Anju Raghunathrao, Kapre; KAU; Nanu, EIn the present study an effort has been made to assess the bacteriological quality of raw milk obtained from three different sources in Trichur. A total of 21 individual and seven pooled samples were collected from each sources (S1, S2 and S3), over a period of five months. The samples were subjected to different bacterial counts and also for the isolation and identification of S. aureus and E. coli. The isolates were tested for their sensitivity to various chemotherapeutic agents. The average total viable count of individual milk samples from S1, S2 and S3 were 7.5 x 104, 1.4 x 105 and 2 x 105 CFU per ml respectively. Significant difference (P < 0.01) between the counts from S1 and S2; and S1 and S3 was noticed. The average coliform count for S1 was 2.4 x 10, for S2 was 4.8 x 104 and for S3 was 3.8 x 103 CFU per ml. There was significant difference (P < 0.01) between the counts from S1 and S2 ; S1 and S3 ; and S2 and S3. The average counts for thermotolerant coliforms in samples from S1, S2 and S3 were 2.2 x 10, 2.4 x 104 and 2.4 x 103 CFU per ml. The counts from S1 and S2 ; and S1 and S3 differed significantly (P < 0.01). The average faecal streptococcal counts for the sample from S1, S2 and S3 were 1.5 x 102 , 2.1 x 103 and 1.7 x 103 CFU per ml. Significant difference (P < 0.01) between the counts from S1 and S2 , and S1 and S3 was noticed. The staphylococcal counts in samples from S1, S2 and S3 averaged 5.7 x 102, 2.8 x 103 and 6.8 x 103 CFU per ml respectively. Significant differences (P < 0.01) between the counts from S1 and S2 , and S1 and S3 were noticed. The average S. aureus count in samples from S1 was 8.5 x 10, from S2 it was 1.8 x 102 and from S3 , 7.1 x 10 CFU per ml. The average E. coli counts in samples from S1, S2 and S3 were 2 x 102, 1.2 x 104 and 1.5 x 103 CFU per ml respectively. The counts in samples from S1 and S2 ; S1 and S3 ; and S2 and S3 differed significantly (P < 0.01). The average total viable count in pooled milk samples from S1 , S2 and S3 were 4 x 104 , 1.8 x 106 and 2.1 x 105 CFU per ml respectively. Significant difference (P < 0.01) between the counts from S1 and S2 and S1 and S3 was noticed. The average coliform counts at 370C of incubation in the pooled samples from S1, S2 and S3 were 5.5 x 10, 2 x 105 and 6.4 x 103 CFU per ml respectively. The counts from S1 and S2, S1 and S3 ; and S2 and S3 were found significantly different (P < 0.01). The average thermotolerent count in samples from S1, S2 and S3 were 2.8 x 10, 3.6 x 104 and 4.4 x 103 CFU per ml respectively. Significant difference (P < 0.01) in the counts of S1 and S2 ; and S1 and S3 was noticed. The average faecal streptococcal count in samples from S1, S2 and S3 were 2 x 102, 4.8 x 103 and 2.9 x 103 CFU per ml respectively. Significantly different (P < 0.01) counts were noticed between S1 and S2 ; and S1 and S3 was noticed. The average staphylococcal count in samples from S1 was 9.2 x 102 from S2 was 5.3 x 104 and from S3 was 1.3 x 104 CFU per ml. The counts in samples from S1 and S2 ; and S1 and S3 were significantly different (P < 0.01). The S. aureus counts in milk samples from S1, S2 and S3 averaged 1 x 102, 4.8 x 102 and 1.1 x 102 CFU per ml respectively. The average E. coli count in samples from S1, S2 and S3 were 2.7 x 102, 8.9 x 104 and 1.9 x 103 CFU per ml respectively. Significant difference (P < 0.01) between the counts of samples from S1 and S2 ; S1 and S3 ; and S2 and S3 was observed. All the individual samples from S1 were either of very good or good grades (95.24 and 4.76%) respectively. All the pooled milk samples from this source was of very good grade. Most of the individual samples from S2 were of very good or good grades ( 76.20 and 23.80%) respectively, but the pooled milk samples from S2 were of very good, good, fair and poor grades (42.84, 28.60, 14.28 and 14.28%) respectively. Among the individual samples from S3 source all were of either very good or good grades (80.95 and 19.05%) respectively. Pooled milk samples from the same source had very good and good grade (57.14 and 42.86%) respectively. None of the samples from this source were of fair or poor grades. Of the 60 suspected colonies isolated, 54 were identified as S. aureus. Antibiogram of S. aureus isolates showed highest sensitivity to cloxacillin (100%) and gentamicin (100%) followed by amoxicillin (87.03%), chloramphenicol (77.80%) and penicillin – G (35.20%). Of the 70 suspected colonies isolated 66 were identified as E. coli. The E. Coli. Isolates were most sensitive to gentamicin (96.96%) followed by amplicillin (93.92%), furazolidone (80.30%) and carbenicillin (15.155). Doxycycline was least effective drug with no sensitivity and high resistance (90.90%).ThesisItem Open Access Pathology of hypothyroidism in pigs(Centre of Excellence in Pathology, College of Veterinary and Animal Sciences,Mannuthy, 1995) Prasanna, K S; KAU; Sreekumaran, TAn experimental model of hypothyroid state was induced in piglets, using thiourea with the objectives of studying the sequence of clinico pathological changes and its influence on the animal health and growth. Tweleve Large White Yorkshire male piglets of 2 – 3 months age were selected for the study. The animals were divided into control group of six animals and experimental group of six animals. Experimental hypothyroidism was induced by feeding thiourea daily for a period of three months at the dose level of 50 mg per kg body weight. Haemogram, body weight, plasma proteins, serum cholesterol and serum thyroxine values were estimated at periodic intervals. The piglets were subjected to detailed autopsy after sacrifice. Gross lesions were recorded and detailed histopathological examination of tissues was carried out. During the course of experiment all the experimental animals recorded stunted growth and appreciable reduction in feed intake and alopecia of neck and shoulder regions. There was significant increase in blood cholesterol values and plasma protein level in thiourea fed group. A significant reduction in serum thyroxine level was also recorded. There was significant increase in the relative weight of thyroid, adrenal and pituitary glands of experimental animals. Gelatinisation of subcutaneous fat and dilatation of right ventricles were common findings at autopsy. Histologically the thyroid glands exhibited varying degree of hyperplastic changes and depletion of colloid in the follicles. Hyperplasia and hypertrophy of the lining epithelium was also observed. Predominant histological changes in the pituitary was hyperplasia and hypertrophy of the basophil cells and degranulation of the acidophil cells. Adrenal glands showed diffuse hyperplasia of zonafasiculata and accessory cortical nodule formation. Skin revealed acanthosis, hyperkeratosis and keratinisation of harifollicles. In all the hypothyroid animals testis showed varying degree of tubular degeneration. A random survey study was conducted to assess the thyroid status of pigs from different parts of Kerala using serum thyroxine as the marker. This concluded that most of the animals had the normal range of serum thyroxine levels.ThesisItem Open Access Microbial degradation of mimosine in goats(Department of Animal Nutrition, College of Veterinary and Animal Sciences,Mannuthy, 1995) Prabhakaran, P; KAU; Devasia, P AAn investigation was carried out to find out the extent of in vitro microbial degradation of pure mimosine (T1) and that of immature leaves (T2), mature leaves (T3), tender stems (T4) and seeds (T5) of L. leucocephala using strained rumen liquor obtained from three rumen fistulated Saanen – Malabari crossbred goats maintained under standard conditions of feeding and management. The proximate chemical composition and mimosine content of different edible parts of leucaena during the months of May, June and July were determined. While immature leaves and seeds had higher crude protein content, seeds had higher crude fat, tender stems had higher crude fibre and mature leaves had higher ash content compared to other edible parts of subabul. The average mimosine concentrations of T2, T3, T4 and T5 were 12.11 + 0.05, 4.89 + 0.02, 3.90 + 0.04 and 10.70 + 0.08 per cent respectively during May; 11.66 + 0.06, 5.23 + 0.03, 3.62 + 0.03 and 10.44 + 0.05 per cent respectively during June and 9.96 + 0.05, 4.92 + 0.03, 3.73 + 0.02 and 9.51 + 0.04 per cent respectively during July on a dry matter basis. The average mimosine concentrations of strained goat rumen liquor incubated with 37.50 mg/100 ml of added mimosine in pure form or as immature leaves, mature leaves, tender stems and seeds showed significant reduction at every 12 hr intervals from 0 to 48 hr of incubation, the final average concentrations being 23.98 + 0.37, 23.14 + 0.37, 22.20 + 0.28, 23.12 + 0.52, 23.35 + 0.37 mg/100 ml of SRL. The percentage of in vitro degradation in respect of T1, T2, T3, T4 and T5 increased significantly at every 12 hr intervals of incubation from 0 to 48 hr, even though the degradation was incomplete with all treatments, the average percentage degradation at 48 hr of incubation being 31.69 + 1.02, 34.49 + 1.18, 37.12 + 0.99, 34.54 + 1.50 and 33.41 + 1.03 respectively. The overall average rate of disappearance of mimosine in µg.ml-1 . h-1 in respect of T1, T2, T3, T4 and T5 for the entire period of 48 hr of incubation were 2.33, 2.54, 2.74, 2.54 and 2.44 respectively with highest rates during 0 to 12 hr, lower rates during 24 to 36 hr and least rates during 36 to 48 hr. The production of ammonia and VFA coincided with the active degradation of mimosine, there being faster degradation upto 12 hr of incubation with highest concentrations of ammonia and VFA at 12 hr of incubation. The overall results indicated that the rumen microorganisms of crossbred goats degrade mimosine to DPH, ammonia and VFA and that mimosine does not inhibit the microbial activity, even though the possible role of leucaena endogenous enzymes in the partial degradation of mimosine recorded in the present study cannot be ruled out.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.
