Philopatry and Dispersal Patterns in Tiger (Panthera tigris)

Background

Tiger populations are dwindling rapidly making it increasingly difficult to study their dispersal and mating behaviour in the wild, more so tiger being a secretive and solitary carnivore.

Methods

We used non-invasively obtained genetic data to establish the presence of 28 tigers, 22 females and 6 males, within the core area of Pench tiger reserve, Madhya Pradesh. This data was evaluated along with spatial autocorrelation and relatedness analyses to understand patterns of dispersal and philopatry in tigers within this well-managed and healthy tiger habitat in India.

Results

We established male-biased dispersal and female philopatry in tigers and reiterated this finding with multiple analyses. Females show positive correlation up to 7 kms (which corresponds to an area of approximately 160 km²) however this correlation is significantly positive only upto 4 kms, or 50 km² (r  = 0.129, p<0.0125). Males do not exhibit any significant correlation in any of the distance classes within the forest (upto 300 km²). We also show evidence of female dispersal upto 26 kms in this landscape.

Conclusions

Animal movements are important for fitness, reproductive success, genetic diversity and gene exchange among populations. In light of the current endangered status of tigers in the world, this study will help us understand tiger behavior and movement. Our findings also have important implications for better management of habitats and interconnecting corridors to save this charismatic species.     

Tiger presence in a hitherto unsurveyed jungle of India–the Sathyamangalam forests

Tiger, being a solitary and territorial animal, often tends to move out of protected areas into the surrounding forests. This is especially true in the case of sub-adult animals leading to escalating conflicts and deaths in the surrounding human-dominated landscapes. Unless adequately protected against various human activities, such corridors and surrounding forests will soon disappear, trapping the animals within protected areas with resultant local extinctions. In this paper we ascertain tiger presence, occupancy and numbers in one such partially protected area, the Sathyamangalam forest, located close to better known tiger reserves in India, through non-invasive faecal DNA analysis. Here we highlight the potential of Sathyamangalam as a tiger habitat. Tiger positive faecal samples were considered as evidence to establish occupancy in two different parts of Sathyamangalam, reserve forest and wildlife sanctuary. We collected 103 faecal samples out of which 69 were tiger positive. Species occupancy (psi), was 0.672 (±0.197) with a detection probability of 0.2 (±0.06) in the wildlife sanctuary area; while psi was 0.72 (±0.2) with detection probability of 0.212 (±0.6) in the reserve forest. Further, number of males and females, as determined in our study, was close to the ideal sex ratio in a healthy forest with good prey abundance. This study also highlights the presence of more females in the reserve forest (n = 10) than the wildlife sanctuary (n = 3) possibly indicating lesser disturbance and more prey availability. We recommend that the reserve forest to the north of Sathyamangalam wildlife sanctuary be declared as a tiger reserve. The wildlife sanctuary could serve as a buffer zone between this reserve and Sathyamangalam town which lies to the south of the forest. Proper protection of Sathyamangalam will go a long way in saving the entire landscape and tigers of the Western Ghats of India.     

Genetic evidence of tiger population structure and migration within an isolated and fragmented landscape in Northwest India

Background

Majority of the tiger habitat in Indian subcontinent lies within high human density landscapes and is highly sensitive to surrounding pressures. These forests are unable to sustain healthy tiger populations within a tiger-hostile matrix, despite considerable conservation efforts. Ranthambore Tiger Reserve (RTR) in Northwest India is one such isolated forest which is rapidly losing its links with other tiger territories in the Central Indian landscape. Non-invasive genetic sampling for individual identification is a potent technique to understand the relationships between threatened tiger populations in degraded habitats. This study is an attempt to establish tiger movement across a fragmented landscape between RTR and its neighboring forests, Kuno-Palpur Wildlife Sanctuary (KPWLS) and Madhav National Park (MNP) based on non-invasively obtained genetic data.

Methods

Data from twelve microsatellite loci was used to define population structure and also to identify first generation migrants and admixed individuals in the above forests.

Results

Population structure was consistent with the Central Indian landscape and we could determine significant gene flow between RTR and MNP. We could identify individuals of admixed ancestry in both these forests, as well as first generation migrants from RTR to KPWLS and MNP.

Conclusions

Our results indicate reproductive mixing between animals of RTR and MNP in the recent past and migration of animals even today, despite fragmentation and poaching risk, from RTR towards MNP. Substantial conservation efforts should be made to maintain connectivity between these two subpopulations and also higher protection status should be conferred on Madhav National Park.     

Improved Methods of Carnivore Faecal Sample Preservation,DNA Extraction and Quantification for Accurate Genotyping of Wild Tigers

Background

Non-invasively collected samples allow a variety of genetic studies on endangered and elusive species. However due to low amplification success and high genotyping error rates fewer samples can be identified up to the individual level. Number of PCRs needed to obtain reliable genotypes also noticeably increase.

Methods

We developed a quantitative PCR assay to measure and grade amplifiable nuclear DNA in feline faecal extracts. We determined DNA degradation in experimentally aged faecal samples and tested a suite of pre-PCR protocols to considerably improve DNA retrieval.

Results

Average DNA concentrations of Grade I, II and III extracts were 982pg/µl, 9.5pg/µl and 0.4pg/µl respectively. Nearly 10% of extracts had no amplifiable DNA. Microsatellite PCR success and allelic dropout rates were 92% and 1.5% in Grade I, 79% and 5% in Grade II, and 54% and 16% in Grade III respectively. Our results on experimentally aged faecal samples showed that ageing has a significant effect on quantity and quality of amplifiable DNA (p<0.001). Maximum DNA degradation occurs within 3 days of exposure to direct sunlight. DNA concentrations of Day 1 samples stored by ethanol and silica methods for a month varied significantly from fresh Day 1 extracts (p<0.1 and p<0.001). This difference was not significant when samples were preserved by two-step method (p>0.05). DNA concentrations of fresh tiger and leopard faecal extracts without addition of carrier RNA were 816.5pg/µl (±115.5) and 690.1pg/µl (±207.1), while concentrations with addition of carrier RNA were 49414.5pg/µl (±9370.6) and 20982.7pg/µl (±6835.8) respectively.

Conclusions

Our results indicate that carnivore faecal samples should be collected as freshly as possible, are better preserved by two-step method and should be extracted with addition of carrier RNA. We recommend quantification of template DNA as this facilitates several downstream protocols.