Technical Reports/Books/Manuals

Permanent URI for this communityhttp://192.168.202.180:4000/handle/123456789/7

Browse

Search Results

Now showing 1 - 2 of 2
  • Item
    Ecological Reconnaissance and conservation assessment of avifauna in Sahyadri Tiger Reserve
    (Wildlife Institute of India, Dehradun, 2018) Sati, Surabhi; Vishwakarma, Anurag; Singh, Ashutosh; Ben, Clement; Gopi, G.V.
    The Western Ghats have been designated a World Heritage Site by UfiESCO because of their Outstanding Universal Values (OUVs), and they support several threatened plant and animal species. The birds of the Western Ghats have received a great deal of academic and conservation attention because of their endemism and the conservation threats they face. However, SUM MAR Y there is only limited empirical ecological information on the avifauna of Sahyadri Tiger Reserve (STR). Hence, a systematic study of the avifauna 'lias required to fill the existing knowledge gap and for long-term conservation. This study was initiated in collaboration with STR, Maharashtra and Wildlife Institute of India. The study was conducted between October 2015 and February 2018. The area was divided into four major habitat types, namely agriculture land, grassland, shrubland and forest. The aim of the study was to assess the conservation importance of STR with respect to the avifauna by, understanding the diversity, abundance and habitat utilization in relation to the anthropogenic pressure in different seasons (autumn, winter, summer) . Systematic field data were collected using the point count method to determine the distribution and abundance of species. The bird species, number of individuals (male, female and juvenile), habitat variables, vegetation characteristics and disturbance variables were recorded and quantified. The bird abundances and diversities of the different habitat types were compared and related to habitat features. Bird densities were estimated using the distance sampling method. The Shannon-Wiener diversity index (H') was used to determine the species diversity. The Spearman correlation coefficient was used to determine the relationship between the bird abundance and the habitat features within habitat types. A total of 218 species of bird belonging to 55 families were recorded during the study. Seven of these are threatened species. The highest number of recorded species (30) was in the family Accipitridae. Seven endemic birds of the Western Ghats were also recorded. We found that there is a significant relation between the bird density and diversity within a habitat type across the three sampling seasons. In autumn, the density ranged from 733. 7 5 ± 63.14 to 485 .91 ±46.01 per Kml. The highest density was recorded in agriculture land and the lowest in forest. In winter the density ranged from 1573.3 ± 90.27 to 519.83 ± 31.43, the highest being in agriculture land and the lowest in forest. In summer the density ranged from 900.59 ± 58.58 to 403.00 ± 39.97, the highest being in shrubland and the lowest in grassland. The study found higher bird densities in autumn and winter in areas with highly intense agriculture activities as human disturbed areas such as agriculture areas provide heterogeneous habitats that attract human-tolerant bird species. It was also observed that during summer, shrubland had the highest density of birds whereas the lowest density was in grassland and agriculture land. In summer the grasslands and agriculture lands were usually dry. Farmers burn field residues, and hence shrubland provided a more open habitat that supports shrubs that provide food and canopy cover for different bird species. Unlike the bird density, the diversity of the avifauna was high in forest in all three seasons. In autumn, the diversity index values ranged from 3.867 to 3.533, and in winter the diversity index values ranged from 3.895 to 3. 551.ln summer the diversity index values ranged from 3. 941 to 3. 258. The diversity was highest in forest and lowest in grassland in all three seasons. We observed unusual flowering of the Dhak, Butea monosperma (Lam.) Taub. (Fabaceae). The flowering time of the species is March-April though sometimes it also flowers in late February and the flowering lasts till early May. Notably, during our of the field surveys, we observed 10 fully grown individuals of B. monosperma in full bloom from mid November to late December in Chandoli National Park and Koyna Wildlife Sanctuary. Through continuous monitoring of these individuals in the tiger reserve t:le confirmed unusual phenological events that have not been reported earlier for this species. The change in phenological events of this species could be attributed to climatic change, irregular drought patterns or genetic factors, albeit further research is needed. The study reveals the relationship between avifauna species richness and habitat patterns and addresses the effects of anthropogenic pressure on avian species richness and its distribution patterns. Also, this study provides evidence that settlement are as can serve as refuges for birds. Therefore, conservation efforts should be directed towards making communities view human-occupied areas as habitats for birds and not as lost habitats. Hence scientific understanding backed by empirical evidence about the process and patterns of avifaunal assemblages in STR can be used to formulate a robust conservation plan for the birds of the reserve.
  • Item
    Ecology of leopard Panthera pardus in relation to prey abundance and land use pattern in Kashmir Valley
    (Wildlife Institute of India, Dehradun, 2014) Habib, Bilal; Gopi, G.V.; Noor, Athar; Mir, Zaffar Rais
    Globally, leopard (Panthera pardus) is the most widely distributed and persecuted cat amongst large cat species. In India, it largely coexists with other feline species like the tiger (Panthera tigris) across much of its distribution range and with lion (Panthera leo) and clouded leopard (Neofelis nebulosa) in certain areas of its distribution range. Owing to its very high adaptability for surviving in varieties of habitats and opportunistic feeding behavior, it is often found to be at the center of the human-wildlife conflict. Retaliatory persecution, poaching, habitat loss and declining natural prey are some of the factors which lead to its population decline, despite being accorded protection through national and international legislations. In Kashmir Himalayas it is at the top of the food chain and an apex predator that aids in regulating prey populations. However, there has been an increase in the human-leopard conflicts in the valley which, if left unnoticed, will worsen the conservation prospects of this threatened felid. Hence, this long term study was initiated to address two major issues: 1. Conservation and management planning of the leopards in the valley is impeded by the paucity of reliable empirical ecological information and 2. Current threat levels will have to be assessed to understand and predict the impacts of anthropogenic pressure on leopards. The objectives of the study were to estimate leopard population and prey abundance, to study the leopard feeding habits and to determine the ranging behavior of leopards. Dachigam National Park was selected to undertake ecological studies on leopards. Only the lower Dachigam was chosen as an intensive study area as the upper reaches of Dachigam are mostly high alpine areas where leopards do not inhabit. In order to study prey abundance, line transect methodology was adopted. Transects (n = 13) were laid and monitored in the study area to obtain seasonal prey abundance. In order to estimate smaller prey (rodents) abundance, Sherman traps (n = 49) were used to estimate density. Feeding habits of the leopards were studied by collecting leopard scats (n = 714) which were later analysed using standard protocols. The population of leopard in the study area was estimated using camera traps (n = 12 pairs), deployed in 2x2 km grids in the study area to individually identify leopards with their unique coat patterns. The ranging pattern of leopards was studied by tracking the leopards (n = 3) fitted with Vectronics GPS collars. Amongst large prey, Himalayan grey langur and Hangul were sighted with enough records to be amenable to analysis in program DISTANCE version 6.0. In total 170 groups of langur comprising of 2679 individuals and 206 groups of hangul comprising of 829 individuals were sighted across different seasons in the study area. Overall density (±SE) of langur was estimated to be 16.32 ± 1.87 km ² and of hangul 5.11 ± 0.51 km-² in the study area. Langur density was highest (22.05 ± 5.12/km²) in winter season and lowest (9.35 ± 3.03/km²) in summer season whereas, Hangul density was found to be highest (9.51 ± 1.71/km²) in spring season and lowest (2.31 ± 0.51/km²) in summer season. In case of rodents, the density was found to be highest during summer season (2014 ± 830.71/km²) and lowest during winter season (1172.6 ± 442.74/km²). In case of dietary spectrum of leopard in Dachigam, small rodents contributed the maximum (48.05%) in terms of percent frequency of occurrence followed by langur (14.04%). Hangul contributed 2.05% while Himalayan serow contributed only 0.20% and rhesus macaque contributed the least (0.10%) to the diet of leopard. Minimum sample size required to study food habits of leopard varied from 66 to 86 scat samples in different seasons. Jacobs' index calculated from biomass availability and biomass consumption indicates that small rodents and langur were preferred in all the four seasons. Preference of hangul was slightly higher (-0.79) during winter season as compared to summer season (-0.90). A total of 396 trap nights resulted in a total of 14 leopard photographs with 3 individual leopards. Amongst the three individuals, 2 males and 1 female was photo-captured. Although, the Null (M ) model 0 was selected based on highest criterion score, we selected the Heterogeneity (M ) model because h leopards are territorial animals and it accounts for heterogeneous capture pobabilities between individuals. The density estimate produced by average home range radius (HHR) was 2.11 ± 1.06 2 individuals per 100 km which was found best as density of the leopard in the study area. The relative abundance index of the leopard in the sampling duration turned out to be 3.5 per 100 trap nights. The maximum home range (100% MCP) of the 2 female F74 was ~ 74 km which was recorded during summer season. The summer home range (100% MCP) of the male was 1.96 times larger than the female leopard. The least home range (~ 41.4 2 km ; 100% MCP) came up during the winter season. The increasing trend represented by the ranges (100% MCPs) of this female was winter < spring 2 2 (48.42 km ) < autumn (67.9 km ) < summer. The leopards showed large variation in daily distances moved during the lean season of summer. Daily displacements of the leopards were not normally distributed Kolmogorov-Smirnov Test) for the male: M73 (D = 0.119, df = 105, p = 0.001), female: F71 (D = 0.191, df = 105, p = 0.000) and female: F74 (D = 0.092, df = 105, p = 0.029). Daily displacement was longer for the male leopard (median displacement = 588 m) than the female leopard (median displacement = 367.44 m). The total distance travelled by the male leopard (398.71 km) was greater than the female leopards: F74 (374.16 km) and F71 (62.91 km). In case of female leopard F74, the median daily distance travelled was highest during the winter season (0.664 km) followed by autumn (0.528 km), spring (0.506 km) and summer (0.367 km) Findings of this study indicate that leopards are facing prey scarcity in the area, thus making them to rely upon suboptimal prey and occupy home ranges larger than other studies in the subcontinent. Leopards being opportunistic feeders have also started feeding on domestic prey in absence of sufficient wild prey, thereby elevating the human - leopard conflict in the region. Human - animal conflict being the major threat to large carnivores all across their distribution range is a big impediment in leopard conservation in he study area as well. 1. Estimation of prey density across different sites and developing a relationship between density of prey base and leopard abundance. 2. Study variation of food habits across different sites and seasons in Kashmir valley. 3. Estimate density, abundance and distribution of leopard across different study sites. 4. Study movement pattern, home range size and social organization of leopards across different sites