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20 results for “Panthera tigris”
Fig. 2 in Camera Trapping The Indochinese Tiger, Panthera Tigris Corbetti, In A Secondary Forest In Peninsular Malaysia
Fig. 2. Cumulative number of individual tiger captured per month around FELDA Jerangau Barat, Terengganu between April 2000 to September 2000.
Fig. 3 in Camera Trapping The Indochinese Tiger, Panthera Tigris Corbetti, In A Secondary Forest In Peninsular Malaysia
Fig. 3. Identification of tiger individuals from infra-red sensor camera traps. Example of individual identification of tiger cubs (a, b) and adults (c, d) based on stripe patterns.
Figure 1 in Population structure and spatial distribution of the tiger (Panthera tigris, Felidae, Carnivora) in Southwestern Primorye (Russian Far East)
Figure 1. Census routes and places of encounters of tiger tracks in study area: blue dots, during the expedition surveys; red dots, during monitoring of the model site.
Figure 4 in Population structure and spatial distribution of the tiger (Panthera tigris, Felidae, Carnivora) in Southwestern Primorye (Russian Far East)
Figure 4. Distribution of tigers in the Amba, Barabashevka, and Narva River watersheds according to photoidentification results.
Fig. 5 in Cerebral cysticercosis in a wild Bengal tiger (Panthera tigris tigris) in Bhutan: A first report in non-domestic felids
Fig. 5. Cladogram showing the relation between the sequence of the nad1 gene (491bp) amplified from the sediment of the 21 μm filter of the sieving method for isolation of taeniid eggs from faeces of the tiger analysed in this study highlighted in bold (MT920328); together with the sequence of the same gene of different Taenia spp.
Fig. 4 in Cerebral cysticercosis in a wild Bengal tiger (Panthera tigris tigris) in Bhutan: A first report in non-domestic felids
Fig. 4. Cladogram showing the relation between the sequences of the cytB gene of Taenia solium from the present study highlighted in bold (MT371084- MT371085) and unique published sequences of the cytB gene available in GenBank from Ecuador (ECU), Tanzania (TANZ), Mexico (MEX), Brazil (BRA), Cameroun (CAM), Thailand (THA), Indonesia (INDO), Madagascar (MDG), INDIA, China (CHI) and Nepal (NEP). The sequences for the cytB gene from Taenia saginata (AB066581) and Taenia asiatica (AB066580) are also included. The cytB sequence from Echinococcus multilocularis (MK843307) was used as an outgroup.
Fig. 1 in Cerebral cysticercosis in a wild Bengal tiger (Panthera tigris tigris) in Bhutan: A first report in non-domestic felids
Fig. 1. Camera trap image of the tiger infected with Taenia solium reported in this article captured on the 15th of November 2014. The image was taken during a survey of the Bengal tiger population at national level in Bhutan. Copyright: Nature Conservation Division, DoFPS, MoAF, Bhutan.
Fig. 2 in Cerebral cysticercosis in a wild Bengal tiger (Panthera tigris tigris) in Bhutan: A first report in non-domestic felids
Fig. 2. Cysts identified at necropsy of the Bengal tiger in Bhutan (left) and isolated in a jar (right).
Fig. 3 in Cerebral cysticercosis in a wild Bengal tiger (Panthera tigris tigris) in Bhutan: A first report in non-domestic felids
Fig. 3. Cladogram showing the relation between the sequences of the cox1 gene of Taenia solium from the present study highlighted in bold (MT366763- MT366764) and unique published sequences of the cox1 gene available in GenBank from Tanzania (TANZ), Brazil (BRA), Mexico (MEX), Ecuador (ECU), Madagascar (MDG), Indonesia (INDO- PA, INDO-BA), China (CHI), Nepal (NEP), Thailand (THA) and India (TAE). Sequences for the cox1 gene from Taenia saginata (AB066495) and T. asiatica (AB066494) were also included. The cox1 sequence of Echinococcus multilocularis (MN251845) was used as an outgroup.
Figure 3 in First photographic evidence of Panthera tigris from Neora Valley National Park, Central Himalayas, India
Figure 3. Recorded tiger left view at Kattus Dara, Neora Valley National Park.
Figure 1 in First photographic evidence of Panthera tigris from Neora Valley National Park, Central Himalayas, India
Figure 1. Map of Neora Valley National Park with camera trap location.
Fig. 1 in Camera Trapping The Indochinese Tiger, Panthera Tigris Corbetti, In A Secondary Forest In Peninsular Malaysia
Fig. 1. Map of FJB and infra red sensored camera locations.
Figure 5 in Population structure and spatial distribution of the tiger (Panthera tigris, Felidae, Carnivora) in Southwestern Primorye (Russian Far East)
Figure 5. Layout of home ranges of the GPS-collared tigers (Hernandez-Blanco et al., 2015).
Figure 3 in Population structure and spatial distribution of the tiger (Panthera tigris, Felidae, Carnivora) in Southwestern Primorye (Russian Far East)
Figure 3. Relationship between tigers according to DNA identification.
Figure 2 in Population structure and spatial distribution of the tiger (Panthera tigris, Felidae, Carnivora) in Southwestern Primorye (Russian Far East)
Figure 2. Distribution of tiger tracks in Southwestern Primorye.
The indigenous range of the tiger (Panthera tigris)
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Data from: Fine-scale population genetic structure of the Bengal tiger (Panthera tigris tigris) in a human-dominated western Terai Arc Landscape, India
Despite massive global conservation strategies, tiger populations continued to decline until recently, mainly due to habitat loss, human-animal conflicts, and poaching. These factors are known to affect the genetic characteristics of tiger populations and decrease local effective population sizes. The Terai Arc Landscape (TAL) at the foothills of the Himalaya is one of the 42 source sites of tigers around the globe. Therefore, information on how landscape features and anthropogenic factors affect the fine-scale spatial genetic structure and variation of tigers in TAL is needed to develop proper management strategies for achieving long-term conservation goals. We document, for the first time, the genetic characteristics of this tiger population by genotyping 71 tiger samples using 13 microsatellite markers from the western region of TAL (WTAL) (1800 km2). Specifically, we aimed to estimate the genetic variability, population structure, and gene flow. The microsatellite markers indicated that the levels of allelic diversity (MNA = 6.6) and genetic variation (Ho =0.50, HE = 0.64) were slightly lower than those reported previously in other Bengal tiger populations. We observed moderate gene flow and significant genetic differentiation (FST= 0.060), and identified the presence of cryptic genetic structure using Bayesian and non-Bayesian approaches. There was low and significantly asymmetric migration between the two main subpopulations of the Rajaji Tiger Reserve and the Corbett Tiger Reserve in WTAL. Sibship relationships indicated that the functionality of the corridor between these subpopulations may be retained if the quality of the habitat does not deteriorate. However, we found that gene flow is not adequate in view of changing land use matrices. We discuss the need to maintain connectivity by implementing the measures that have been suggested previously to minimize the level of human disturbance, including relocation of villages and industries, prevention of encroachment, and banning sand and boulder mining in the corridors.
Data from: Fine-scale population genetic structure of the Bengal tiger (Panthera tigris tigris) in a human-dominated western Terai Arc Landscape, India
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On following pages: 4. Tiger (Panthera tigris). in Felidae
On following pages: 4. Tiger (Panthera tigris).
Figure 2 in First photographic evidence of Panthera tigris from Neora Valley National Park, Central Himalayas, India
Figure 2. Recorded tiger back view at Kattus Dara, Neora Valley National Park.
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