The productivity of a population of scavenging village chickens in Sri Lanka has been assessed, and the scavenging feed resource base has been measured and analysed. The laying period lasted 34 +/- 13 days and the batch size was about 20 eggs. The households ate 71% of the egg production. The mean egg weight was 48 g and the mean size of a set of eggs was 9.4. The hatching percentage was 67 +/- 32 and the liveweight at 70 days averaged 313 g with a range of 142 to 492, by which time 65% of the chicks hatched had died. The age at first lay averaged 211 days when the pullets weighed 1,160 g. The broody period lasted from 3 weeks to 4 months depending on whether the hen hatched eggs, and for how long she tended the brood. The laying hens were actively scavenging for most of the daylight hours. The average amount of scavenged feed per household flock per day was 550 g dry weight with a proximate composition of 9.4% crude protein, 9.2% ether extract and 5.4% crude fibre. More than 70% of the feed intake was household refuse (27% cooked rice, 30% coconut residue, 8% broken rice and 36% other scraps). The remainder was from the environment (13% grass shoots, 8% small metazoans and 7% paddy rice). Proximate analyses of crop contents, household refuse and its major components were carried out. Dietary Ca and P levels were low in the village, as were plasma levels of these minerals. On a balanced commercial diet plasma Ca was still lower than that of hybrid commercial chickens. Suggestions are made for improving the productivity of the scavenging system with no requirement for inputs, and with inputs.

A polymerase chain reaction (PCR) assay was developed to differentiate meat of Ceylon spotted deer (Axis axis ceylonensis), Ceylon hog deer (A. porcius oryzus), Ceylon sambhur (Cervus unicolor unicolor) and barking deer (Muntiacus muntijak malabaricus) from meat of cattle, goat, buffalo, pig, dog and sheep. A set of primers was designed according to the sequence of the mitochondrial cytochrome b gene of C. elaphus canadensis and by PCR amplification about 450 bp band was observed for all four animal species and these primers were not cross reacted with DNA of other animal species tested in the study under the tested reaction conditions. A band of 649 bp size was observed for all animal species when DNA was amplified with the universal primers and that indicated the presence of mitochondrial DNA in the samples. Further, the results indicated that this technique was sensitive enough to differentiate rotten meat, at least 5 days after the killing of an animal. Under these PCR conditions, the DNA of bacteria, which is involved in decomposition of meat, was not amplified with both universal and specific primers. However, the method was not sensitive enough in differentiating cooked meat of these species. Slaughtering of these four wild animal species is banned, but the animals are being killed illegally. Lack of meat identification methods has been identified as one of the major constraints to implement legal procedures and conserve biodiversity in the country.

A polymerase chain reaction (PCR) assay was developed to differentiate buffalo meat from the meat of Ceylon spotted deer (Axis axis ceylonensis), Ceylon sambhur (Cervus unicolor unicolor), cattle (Bovine), goat (Caprine), pig (Porcine), and sheep (Ovine). A set of primers were designed according to the sequence of the mitochondrial cytochrome b gene of bubalus bubalis and by PCR amplification a band of approximately 242 bp band was observed with buffalo DNA. These primers did not cross-react with DNA of other animal species tested in the study under the specified reaction conditions. A band of 649 bp was observed for all animal species tested when DNA was amplified with the universal primers indicating the presence of mitochondrial DNA in the samples. The technique was sensitive enough to identify rotten (10 days post slaughter), dried and cooked buffalo meat. The absence of a cross reaction with human DNA using the buffalo specific primers eliminates possible false positive reactions.

Sri Lanka is a tropical nation within a zoogeographic zone that is at high risk for infectious disease emergence. In 2010, a study was conducted on the feasibility of enhancing capacity in Sri Lanka to manage wildlife diseases through the establishment of a national wildlife health centre. The Canadian Cooperative Wildlife Health Centre was assessed as a potential model for adaptation in Sri Lanka. Interviews and group meetings were conducted with potential key participants from the Sri Lankan Departments of Wildlife Conservation and Animal Production and Health, and the Faculty of Veterinary Medicine and Animal Science of the University of Peradeniya. In addition, site visits were made to potentially participating facilities and the literature on best practices in building scientific capacity was consulted. With strategic enhancements in education and training, additional personnel, improvements in transportation and diagnostic facilities, and central coordination, Sri Lanka appears very well positioned to establish a sustainable wildlife health centre and programme.