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33 results for “Trachypithecus”
Fig. 4 in Diet of the Annamese langur (Trachypithecus margarita) (Elliot, 1909) at Takou Nature Reserve, Binh Thuan Province, Vietnam
Fig. 4. Food items consumed by Trachypithecus margarita at Takou Mountain in the morning (n = 1478) and afternoon (n = 2568).
Figure 3 in Ecological conditions of Javan langur (Trachypithecus auratus É. Geoffroy Saint-Hilaire, 1812) in Sokokembang Forest (Central Java, Indonesia) through distribution and food preferences
Figure 3. Percentage composition of plant parts eaten by Javan langurs in Sokokembang forest.
Figure 4 in Ecological conditions of Javan langur (Trachypithecus auratus É. Geoffroy Saint-Hilaire, 1812) in Sokokembang Forest (Central Java, Indonesia) through distribution and food preferences
Figure 4. Distribution map of Javan langur food plants.
Figure 1 in Ecological conditions of Javan langur (Trachypithecus auratus É. Geoffroy Saint-Hilaire, 1812) in Sokokembang Forest (Central Java, Indonesia) through distribution and food preferences
Figure 1. Location of Sokokembang forest, Pekalongan Regency, Central Java, Indonesia.
Figure 5 in Ecological conditions of Javan langur (Trachypithecus auratus É. Geoffroy Saint-Hilaire, 1812) in Sokokembang Forest (Central Java, Indonesia) through distribution and food preferences
Figure 5. Percentage of canopy stratum utilization by Javan langurs in Sokokembang forest.
Fig. 1 in Diet of the Annamese langur (Trachypithecus margarita) (Elliot, 1909) at Takou Nature Reserve, Binh Thuan Province, Vietnam
Fig. 1. Location of study site (star) on Takou Mountain in Takou Nature Reserve.
Data from: Low genetic diversity and strong population structure shaped by anthropogenic habitat fragmentation in a critically endangered primate, Trachypithecus leucocephalus
Habitat fragmentation may strongly impact population genetic structure and reduce the genetic diversity and viability of small and isolated populations. The white-headed langur (Trachypithecus leucocephalus) is a critically endangered primate species living in a highly fragmented and human-modified habitat in southern China. We examined the population genetic structure and genetic diversity of the species and investigated the environmental and anthropogenic factors that may have shaped its population structure. We used 214 unique multi-locus genotypes from 41 social groups across the main distribution area of T. leucocephalus, and found strong genetic structure and significant genetic differentiation among local populations. Our landscape genetic analyses using a causal modelling framework suggest that a large habitat gap and geographical distance represent the primary landscape elements shaping genetic structure, yet high levels of genetic differentiation also exist between patches separated by a small habitat gap or road. This is the first comprehensive study that has evaluated the population genetic structure and diversity of T. leucocephalus using nuclear markers. Our results indicate strong negative impacts of anthropogenic land modifications and habitat fragmentation on primate genetic connectivity between forest patches. Our analyses suggest that two management units of the species could be defined, and indicate that habitat continuity should be enforced and restored to reduce genetic isolation and enhance population viability.
On following pages: 142. Shortridge's Langur (Trachypithecus shortridgei); 143. East Javan Langur (Trachypithecus 146. Selangor Silvery Langur (Trachypithecus selangorensis); 147. Germain's Langur (Trachypithecus germaini); 148 auratus; 144. West Javan Langur (Trachypithecus mauritius); 145. Silvered Langur (Trachypithecus cristatus));. Annamese Langur (Trachypithecus margarita). in Cercopithecidae
On following pages: 142. Shortridge's Langur (Trachypithecus shortridgei); 143. East Javan Langur (Trachypithecus 146. Selangor Silvery Langur (Trachypithecus selangorensis); 147. Germain's Langur (Trachypithecus germaini); 148 auratus; 144. West Javan Langur (Trachypithecus mauritius); 145. Silvered Langur (Trachypithecus cristatus));. Annamese Langur (Trachypithecus margarita).
On following pages: 152. Indochinese Gray Langur (Trachypithecus crepusculus); 153. Cat Ba Langur (Trachypithecus (Trachypithecus delacouri); 156. Francgois's Langur (Trachypithecus francoisi); 157. Black Langur (Trachypithecus ebenus (Trachypithecus leucocephalus); 155. Delacour's Langur);, Trachypithecus laotum); 159. Hatinh Langur (Trachypithecus hatinhensis). poliocephalus); 154. White-headed Langur 158. Laos Langur ( in Cercopithecidae
On following pages: 152. Indochinese Gray Langur (Trachypithecus crepusculus); 153. Cat Ba Langur (Trachypithecus (Trachypithecus delacouri); 156. Francgois's Langur (Trachypithecus francoisi); 157. Black Langur (Trachypithecus ebenus (Trachypithecus leucocephalus); 155. Delacour's Langur);, Trachypithecus laotum); 159. Hatinh Langur (Trachypithecus hatinhensis). poliocephalus); 154. White-headed Langur 158. Laos Langur (
Data from: Low genetic diversity and strong population structure shaped by anthropogenic habitat fragmentation in a critically endangered primate, Trachypithecus leucocephalus
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Data from: Neglected seed dispersers: endozoochory by Javan lutungs (Trachypithecus auratus) in Indonesia
Leaf monkeys are known to be leaf eaters, and thus, their potential role as seed dispersers has been neglected. However, they do also feed on fruits. To examine the role of leaf monkeys as endozoochorous seed dispersers, we studied the Javan lutung (Trachypithecus auratus) in Indonesia. We compared multiple aspects of seed dispersal processes (amount and diversity of seeds ingested, dispersal distance, and germination rate) of lutungs with that of the sympatric long-tailed macaque (Macaca fascicularis). Over the study period, 54 percent of the lutung feces contained intact seeds, which was equivalent to the macaque feces contained seeds (62%). Seeds of at least six plant species were detected in the lutung feces, which was less than those found in the macaque feces (>19 plant species). The main species of seeds defecated by both lutungs and macaques was Ficus spp. (seed size: 0.7 mm). Seed shadow, estimated from travel distance (range: 1–299 m) and gut passage rate (24–96 h), had a unimodal-distribution with a peak at 51–100 m, and was shorter than that reported in published accounts of macaques and other similar and smaller sized frugivores. Finally, germination rates of Ficus spp. seeds ingested by both lutungs and macaques were lower than that of the control seeds. These results imply that the dispersal effectiveness of lutungs would be lower than that of the sympatric primate frugivores. However, at a population level, lutungs could play a significant role as seed dispersers for the small-seeded species, and therefore, more research into their frugivorous habits is warranted.
Data from: Neglected seed dispersers: endozoochory by Javan lutungs (Trachypithecus auratus) in Indonesia
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Figure 8 in Ecological conditions of Javan langur (Trachypithecus auratus É. Geoffroy Saint-Hilaire, 1812) in Sokokembang Forest (Central Java, Indonesia) through distribution and food preferences
Figure 8. Grooming activities of Javan langurs in Sokokembang forest. Photo by Y.M. Putra.
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