Location of the study
The study was conducted at Regional station of ICAR-Directorate of Poultry research, Bhubaneswar earlier it was Regional Centre, ICAR-Central Avian Research Institute, Bhubaneswar. The climate of the location is hot and humid with annual rain fall average of 200 cm and the average maximum and minimum temperature of 38o C and 280 C, respectively. Sometimes the highest temperature in summer reaches up to 45o C. The location is situated between 20.9517 N latitude and 85.0985o E longitude. The average relative humidity of the location is around 77% although it varies from 68% during winter (January) to 88% during monsoon (July). Most humid month is July with humidity varies from 70.4–97.3%.
Experimental population
The breed of duck used for the present study was Kuzi ducks in its second generation which were being selected for higher eight week body weight in S0 and S1 generation. Kuzi duck collected from different parts of Odisha and a small population of Kuzi ducks available in the Regional Station of ICAR- Central Avian Research Institute, Bhubaneswar (presently under ICAR-Directorate of Poultry Research, Hyderabad) form the base generation of the Kuzi ducks. S1and S2 generations were produced by using 40 sire and 160 dams. Pen mating using 4 dams and 1 sire being used and a total of 40 breeding pen were utilized. The hatching eggs were marked as per the sire number and were set at 7 days interval. Ducklings hatched in seven hatches were wing banded sire wise and the birds having wing band up to 10 weeks (875 numbers) were used for phenotypic characteristics like plumage colour, bill colour, shank colour and for the genetic study. Sexing was done at 8 weeks of age. After 10 and 16 weeks of age most of the male birds were selected according to higher eight week body weight and all the females were kept for growing up to 20 weeks of age. Again after 40 and 52 weeks of age some males and females were discarded having lower body weight at 8 weeks of age and having some deformities. Due to lack of sufficient laying pen after 60 weeks only females of 4 hatches were kept for laying up to 72 weeks of age.
Rearing and management
The ducklings were brooded for 8 weeks under standard brooding practices in an open sided house on deep litter. Initial five days the litter were covered with old news paper and it was replaced with new one every day morning. Whenever the litters were wet it was removed and replaced with dry and fresh litter material. All the hatches were reared separately throughout the experimental period. Litter material use for this experiment was rice husk. During brooding wheat based starter mash having crude protein 20% and ME of 2900 kcal/kg was provided. After selection on 10 weeks on basis of high 8 weeks body weight the selected male and all available female were kept for growing with standard grower management with duck grower ration containing crude protein 16% and ME 2600 kcal/kg. During laying period ducks were fed wheat based diet containing 19% CP and 2600 kcal/kg ME. Layer diets were fed to the ducks at 17 weeks of age. Standard feeding and health care facility during, brooding, growing and laying period were followed. The feed ingredients used in the ration formulations were wheat, soya bean meal, fish meal, deoiled rice bran, salt and vitamin premix, lysine, dl-methionine, trace minerals, shell grit, and di-calcium phosphate. The layer ration was supplemented with extra shell grit so that the calcium content made up to 4.5% of the ration. The birds were provided ad-lib water in tub having water depth of approximately six inches sufficient to immerse their head. Drinking water and feed were provided ad-libitum throughout the experiment. Photoperiod was adjusted to 16 hours per day from 18 weeks of age by providing artificial light during the laying period.
Traits measured
Body weight were measured at day old and then at weekly interval up to 8 weeks of age using a sensitive weighing scale balance with a precision up to 0.5 g. Conformation traits (shank length, keel length and bill length) were recorded at eight weeks of age in both male and female. Plumage colour, bill and shank colour were observed visually for each bird at 8 weeks of age and recorded in the flock. When the bird has more than two colours it was taken as multicolour plumage. When two colours were present in a particular body part observed then the two colours were recorded. The phenotypic features were observed, identified and documented properly. The ducks and drake selected at 10 weeks of age; the body weights during growing were recorded at 10, 12 and 16 weeks of age. Laying period body weights were recorded at 20, 40, 52 and 60 weeks of age. For production parameters like age at first egg of the flock and age of the flock at 20, 50 and 80% duck day egg production per bird of each hatch was taken as a replicate and the average of hatches were calculated. Similarly for number of egg per bird up to 16 weeks, 16–20, 20–40, 40–60, 60–72, 20–72 weeks of age and egg production up to 40, 60 and 72 weeks of age of each hatch was taken as replicate as individual bird egg production were not possible to record on deep litter system. Egg production of each hatch was recorded daily along with number of birds. Egg weights were recorded at 4 weeks interval starting from 20 weeks of age. Efforts were made to record 40 eggs from each hatch from seven days at the particular weeks. So the numbers of eggs recorded for egg weight were different at different weeks of age. Mortality if any was recorded every day.
Egg quality traits were recorded in 80 eggs at 40 weeks of age from the eggs collected at 40 weeks for the first 4 hatches of the flock. For these individual eggs were weighed. Lengths and breadths were measured using a digital vernier caliper. After this the eggs were broken on a flat surface. The height of the albumen was measured half way between the yolk and the edge of the inner thick albumen by using spherometer. Widths of albumen were measured by digital Vernier caliper. The height of yolk with albumen intact was measured along with width. Shape index, albumen index, yolk index and Haugh unit were calculated as per the formula of Shultz (1953), Heiman and Carver (1936), Funk (1948) and Haugh (1937), respectively. There after albumen was separated from yolk and the weight of albumen, yolk and shell with membrane were recorded and their percentages from total egg weight were calculated. Shell thickness with inner membrane and thickness without inner membranes (removing inner membrane manually) were measured at three places of shell (top, middle and bottom) using a paper gauge meter. Shell thickness was calculated taking the average of the three measurements. Yolk color was measured using a DSM yolk fan™ (DSM 2016) as per the guidelines. Different egg quality parameters like shape index, albumen index, yolk index, yolk color, Haugh unit, albumen %, yolk %, Shell %, shell thickness were calculated
Statistical analysis
Juvenile body weight and conformation data were analysed using least square technique (Harvey 1990) with a computer package and the hatch corrected data were utilized for estimating the heritability estimates by variance component analysis (King and Henderson 1954). Genetic and phenotypic correlations were estimated from variance-covariance component analysis (Becker 1975). All other body weight data, production data, egg quality, egg weights data were analysed as per Snedercor and Cochran (1994). Percent of population in collect the data for the traits.