Ontologia
Arctictis binturong

Arctictis binturong

(Raffles, 1822)

VULR Monde (IUCN)
5 photos · Licences CC (Wikimedia Commons / iNaturalist)Click pour agrandir

Description

espèce de mammifères

Source : Wikidata

Pays · région · aire protégée · écorégion · biome
Chargement du graphe…

Indicateurs du réseau écologique

Comment lire ce graphe

Ce graphe représente les interactions écologiques documentées entre Arctictis binturong et d'autres espèces, à partir de la base GloBI (Global Biotic Interactions, agrégation mondiale de la littérature scientifique) — source principale, complétée par d'autres jeux de données d'interactions agrégés par Ontologia. Il faut le comprendre comme une carte du savoir documenté, pas une carte de la réalité écologique exhaustive.

Limites principales

  • Incomplet. La majorité des interactions écologiques en milieu naturel n'ont jamais été publiées. Une espèce sans liens visibles n'est pas isolée — elle est probablement mal étudiée.
  • Biais publication pharmaco-agronomique. La littérature des interactions est polarisée par les enjeux économiques et sanitaires : parasitism / pathogen sur-pondéré sur les mammifères (recherche zoonoses, vecteurs), herbivory sur-pondéré sur les insectes phytophages (entomologie agronomique). À l'inverse, mutualisms, commensalisms et interactions sol/microbiote sont sous-cités. Conseil de lecture : sur les hubs mammifères ou les insectes ravageurs de culture, lire les arêtes parasitism / herbivory dominantes relativement au contexte de littérature, pas comme une mesure d'intensité écologique brute. Détails §10.1.
  • Biaisé vers les espèces étudiées. Quelques espèces (oiseaux communs, abeille mellifère, espèces modèles) concentrent disproportionnellement plus d'interactions documentées. Notre score composite ajoute un malus aux hubs de littérature pour atténuer cette dominance visuelle.
  • Interactions documentées globalement. Toutes les espèces affichées sont observées en France métropolitaine (les observations sont filtrées sur le territoire métropolitain), mais les interactions entre elles proviennent de la littérature scientifique mondiale. Une interaction documentée à l'étranger peut ne pas se réaliser à l'identique sur votre territoire. Le filtre « restreindre à ma commune » tient compte de la co-occurrence spatiale locale mais ne garantit pas l'interaction effective.
  • Sans dimension temporelle. Les variations saisonnières (migration, floraison, cycle de vie) ne sont pas modélisées.
  • Force d'interaction approximative. L'épaisseur des liens reflète le nombre de fois où l'interaction a été rapportée dans la littérature, pas son importance écologique réelle.

Comment nous sélectionnons les espèces affichées

Le graphe affiche au plus 31 nœuds par fiche (1 centre + 15 bulles depth=1 + 15 partenaires depth=2). Le serveur sélectionne intelligemment :

  • Bulles famille créées si une cascade taxonomique existe ou si ≥3 espèces directement documentées partagent une même famille — les espèces sont absorbées dans la bulle (pas de doublon visuel)
  • Espèces individuelles uniquement quand <3 dans une famille (sans cascade) — relations directes documentées
  • Pas d'espèces inférées affichées en doublon — les cascades sont représentées via les bulles famille uniquement
  • Partenaires depth=2 sélectionnés via algo priorité : candidat partagé par ≥2 docs de la famille (food web central) → reliant entre bulles → top sum_obs en dernier recours
  • Sous-types GloBI traduits en français au survol de la flèche (chasse, parasite, parasitoïde, mycorhize…)

Le toggle Profondeur 1 ↔ 2 client-side cache ou affiche les partenaires depth=2 sans refetch. Filtres règne, type d'interaction, ordres/familles, patrimoniales et commune recalculent côté serveur (slow path live ~1-2 s).

Indicateurs avancés (mode expert) : Modularité Q (Newman 2006, PNAS), communautés (Louvain, Blondel et al. 2008, J. Stat. Mech.), nestedness NODF (Almeida-Neto et al. 2008, Oikos).

Source : GloBI · TAXREF v18 (INPN/MNHN) · BDC-Statuts · Wikidata

7 partenaires écologiques documentés directement dans GloBI.

Partenaires
7
Espèces avec interactions documentées
Types d'interactions
3
Prédation, pollinisation, parasitisme…
Connectance
0.095
Densité des liens dans le sous-graphe affiché
Rang animalia
71 %
Percentile vs ensemble des animalia

Liste rouge IUCN

VU · Vulnérablecritères A2cd+3cd+4cdDécroissante
Évaluation complète
Évaluation
2016 · v3.1
Altitude
03000 m
Profondeur
m
État de la populationExpert
Historically, the Binturong was often thought to be relatively common within its distribution range, but it is now mostly uncommon or rare, and is likely to be approaching national extinction in some range countries in mainland South-east Asia (including Viet Nam) and in China. Lekagul and McNeely (1977) stated that it was rare in Thailand, although Nettelbeck (1997) observed it frequently in a small and intensively watched part of Khao Yai National Park. In Lao PDR, there were only three sightings in the extensive wildlife surveys into some of the remotest parts of the country between 1992 and 1999 (Duckworth et al. 1999). Although the species is mostly arboreal, it is detectable using camera-traps, and relatively intensive post-1999 field surveys that have used this method in suitable habitat in protected areas have produced few or no records of this species in Lao PDR (Johnson et al 2009, Coudrat et al. 2014, Gray et al. 2014b), Cambodia (Gray et al. 2014a) and Viet Nam (Willcox et al. 2014: SOM T3), indicating apparently severe declines in these countries. There are very few camera-trap records from Cambodia, although live animals are relatively frequently confiscated from the wildlife trade there (N. Marx per J. Holden pers. comm. 2015). Thailand might be expected to hold one of the healthiest populations in mainland South-east Asia, but declines are suspected there as well (Chutipong et al. 2014). In Myanmar, Than Zaw et al. (2008) confirmed camera-trap records from six survey areas (from Kachin state in the north to Tenasserim in the south), and the species has since been detected in most of the few recent (post-2013) camera-trap surveys in the country, with records from Karen state, Tanintharyi division, and from Tamanthi Wildlife Reserve in Sagaing division (WCS, NWCD, KWCI unpublished data per T.N.E. Gray 2015), suggesting that it might rival Thailand as a core country for the species’s conservation in mainland South-east Asia. There are very few records from Bangladesh, but a camera-trap photograph of an adult with young from the Chittagong Hill Tracts (Chakma 2015), suggests that there is a breeding population at least at this site. In North-east India, it is becoming rarer because of habitat loss, because it seems to prefer mature forest, and is mostly restricted to protected areas in Arunachal Pradesh, Assam, Manipur, Medhalya, Nagaland, Tirupura and Sikkim (Choudhury 2013). It is approaching national extinction in China (Lau et al. 2010).

Binturong was detected by camera-traps in forest surveys across Sabah, Malaysian Borneo, including logged areas, but where logging activities were recent, detections were fewer than in both adjacent primary forest and older logged forest, suggesting a decline in population in logged areas, at least initially (A.J. Hearn, J. Ross and D.W. Macdonald, unpublished data). In Sumatra (Indonesia), the species is probably still widespread in the remaining lowlands in Aceh province and upland forests throughout Sumatra; it is relatively frequently observed and camera-trapped in the Batang Toru forest in North Sumatra, up to 1,000 m a.s.l. (G. Fredriksson unpublished data 2015). Binturong is thought to be relatively common in Kerinci, West Sumatra (Holden 2006, J. Holden pers. comm. 2015). The bones of a Binturong were collected from a snare-trap set for Serow Capricornis sumatrensis at 2,500 m a.s.l. in Kerinci, West Sumatra (Holden 2006). In the Philippines, the species is localized and uncommon (Heaney et al. 1998): populations are thought to be decreasing as a result of collection for the pet trade.

Menaces identifiées(8 menaces classées CMP-IUCN)

  • 2_2_2
    Agro-industry plantations
    Rapid DeclinesMajority (50-90%)Ongoing
  • 5_1_1
    Intentional use (species is the target)
    Rapid DeclinesWhole (>90%)Ongoing
  • 1_1
    Housing & urban areas
    Negligible declinesMinority (<50%)Ongoing
  • 2_1_2
    Small-holder farming
    Negligible declinesMinority (<50%)Ongoing
  • 2_1_3
    Agro-industry farming
    Slow, Significant DeclinesMinority (<50%)Ongoing
  • 2_2_1
    Small-holder plantations
    Slow, Significant DeclinesMajority (50-90%)Ongoing
  • 5_3_3
    Unintentional effects: (subsistence/small scale) [harvest]
    Slow, Significant DeclinesWhole (>90%)Ongoing
  • 5_3_4
    Unintentional effects: (large scale) [harvest]
    Slow, Significant DeclinesMajority (50-90%)Ongoing
Description complète des menacesExpert
Habitat loss and degradation are major threats to the Binturong (Schreiber et al. 1989) as is fragmentation, particularly in those parts of the range where hunting is heavy. Throughout this species's range, there has been loss and degradation of forests through logging and conversion of forests to non-forest land-uses (Sodhi et al. 2010; WWF 2013, 2015; Gaveau et al. 2014). Forest conversion has been extremely high in the lower-altitude parts of its Sundaic range in the last 20 years (e.g. Holmes 2000, BirdLife International 2001, Jepson et al. 2001, McMorrow and Talip 2001, Lambert and Collar 2002, Kinnaird et al. 2003, Curran et al. 2004, Fuller 2004, Eames et al. 2005, Aratrakorn et al. 2006, Gaveau et al. 2014, Margono et al. 2014, Stibig et al. 2014). Protected areas are not exempt from deforestation; 40% of the forest lost in Indonesia during 2000–2012 was lost in areas where logging is restricted (national parks and protected forests; Rode-Margano et al. 2014), and in Kalimantan specifically, 56% of protected lowland forests were cleared from 1985 to 2001 (Curran et al. 2004). Lowland deforestation is now also a growing threat to populations in mainland South-east Asia (e.g. Chutipong et al. 2014, Donald et al. 2015). Choudhury (1997) noted that large-scale deforestation in Indian portions of the species’s range could be contributing to its increased rarity, because many former records come from areas where forests are now being degraded. In China, rampant deforestation and opportunistic logging have fragmented suitable habitat or eliminated sites altogether (Pu et al. 2007).

Throughout South-east Asia, Binturong is hunted for its meat, for traditional medicines and as pets (Corlett 2007, Roberton 2007, Datta et al. 2008, Shepherd 2008, Shepherd and Shepherd 2010, Naniwadekar et al. 2013). In the Philippines, this species is harvested for the pet trade, and in the south of its range it is also taken for human consumption (GMA Philippines 2006). In Lao PDR, this species is among the most frequently displayed caged live carnivores and skins are traded frequently in at least Vientiane (R.J. Tizard pers. comm. to Duckworth et al. 1999, T.N.E. Gray pers. comm. 2015). Considered a delicacy in parts of Lao PDR, the Binturong is taken for food and is also traded as a food item to Viet Nam (I. Johnson pers. comm. to Duckworth et al. 1999). There is a large demand for civet meat, including Binturong, in China and Viet Nam (Bell et al. 2004, Roberton 2007).

Recent camera-trapping evidence across the species’s range has made clear that the Binturong descends to the ground more frequently than had previously been thought; therefore, the threat of snaring to this species is likely to be more serious than had been assumed. Non-specific hunting of large mammals is very high across most of the species's mainland range, with industrial level cable-snaring especially prevalent in parts of northern South-east Asia. Given that the Binturong is relatively unafraid of people and is sometimes active during the day, it is often conspicuous both to surveyors (suggesting that the few encounters reflect a low population) and to hunters (thus exposing it to elevated risk) (Duckworth et al. 1999); this is supported by verbal reports from wildlife hunters in North-east India (see Naniwadekar et al. 2013). A number of national-, landscape- and survey-area-level reviews of small carnivore records in mainland South-east Asia have found Binturong to be infrequently recorded, and sometimes not at all, in relatively intensive camera-trap surveys (i.e. more than 1,000 effective camera-trap-nights) (e.g. Chutipong et al. 2014; Coudrat et al. 2014; Gray et al. 2014a, 2014b; Willcox et al. 2014: SOM T3). Although the species’s arboreality may in part explain the paucity of records, the large number of camera-trap surveys, some of which were targeted at species found in similar habitats e.g. Mainland Clouded Leopard Neofelis nebulosa, and the hunting-pressures in this region that have caused the declines in a large range of animal species, suggests that the current infrequency of Binturong records from the mainland South-east Asia portion of its range may be a genuine indication of its rarity there and that this reflects recent decline.

Habitats préférentiels (classification IUCN)

  • 1_6Forest - Subtropical/Tropical Moist Lowland
  • 1_9Forest - Subtropical/Tropical Moist Montane
  • 14_6Artificial/Terrestrial - Subtropical/Tropical Heavily Degraded Former Forest
  • 1_8Forest - Subtropical/Tropical Swamp
Mesures de conservation recommandéesExpert
Stricter enforcement of legislation against poaching, wildlife trade, habitat degradation and deforestation is required to conserve Binturong. In India it has been on CITES Appendix III since 1989 (CITES 2015). It has also been listed under Schedule I of The Wild Life (Protection) Act of India; this gives the highest conservation status to any species. In Borneo, it is included on Schedule 2 of Sabah’s Wildlife Conservation Enactment 1997, under which hunting and collection is allowed with appropriate license issued by the Sabah Wildlife Department, on Part II of the First Schedule of the Sarawak Wildlife Protection Ordinance 1998, and on Indonesia’s Government Regulation No 7. In Brunei, however, the Binturong is not legally protected. In Bangladesh it has complete protection under wildlife protection law of 2012. It is protected in Malaysia, Thailand (under WARPA 2003), and in Viet Nam (Appendix 1B; Decree 32/2006). In the Philippines, the Environmental Legal Assistance Center has been involved in controlling and enforcing wildlife laws. The species is listed as Critically Endangered on the China Red List.

Binturong occurs in many protected areas spread across its current range; however, the effectiveness of these reserves at protecting this species is highly variable: it has not been targeted as a conservation focus, or indeed even surveyed for, in many protected areas, and most of the confirmed records are from general surveys or by-catch from surveys aimed at other species. Detailed radio-tracking studies, combined with watching to pay particular attention to ground-level use, would aid, greatly, understanding of this species’s ecology and therefore (i) a far more confident assessment of whether the lack of camera-trap records from some areas is a genuine reflection of decline/absence, and not of ineffective camera-trap placement, and (ii) more effectively targeted conservation.
Actions de conservation (11)Expert
  • 1_2Resource & habitat protection
  • 2_1Site/area management
  • 3_1_1Harvest management
  • 3_1_2Trade management
  • 4_2Training
  • 4_3Awareness & communications
  • 5_1_2National level
  • 5_1_3Sub-national level
  • 5_2Policies and regulations
  • 5_4_2National level
  • 5_4_3Sub-national level
Stress écologiques (13)Expert
  • 1_1Ecosystem conversion
  • 1_1Ecosystem conversion
  • 1_1Ecosystem conversion
  • 1_1Ecosystem conversion
  • 1_1Ecosystem conversion
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 2_1Species mortality
Usage & commerce (3)Expert
  • 1Food - human
    nationalsubsistance
  • 10Wearing apparel, accessories
    nationalsubsistance
  • 13Pets/display animals, horticulture
    nationalsubsistance
Priorités de recherche (11)Expert
  • 1_1Taxonomy
  • 1_2Population size, distribution & trends
  • 1_3Life history & ecology
  • 1_4Harvest, use & livelihoods
  • 1_5Threats
  • 1_6Actions
  • 2_1Species Action/Recovery Plan
  • 3_1Population trends
  • 3_2Harvest level trends
  • 3_3Trade trends
  • 3_4Habitat trends
Niche IUCN globaleExpert

Royaumes biogéographiques

Indomalayan

Systèmes (terrestre/eau douce/marin)

Terrestrial
Références bibliographiques (30)Expert
  1. IUCN. 2016. The IUCN Red List of Threatened Species. Version 2016-1. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 30 June 2016).
  2. Donald, P.F., Round, P.D., Thiri Dai'We'Aung, Grindley, M., Steinmetz, R., Nay Myo Shwe and Buchanan, G.M. 2015. Social reform and a growing crisis for southern Myanmar’s unique forests. <i>Conservation Biology</i> 29: 1485–1488.
  3. Chakma, S. 2015. Assessment of large mammals of the Chittagong Hill Tracts of Bangladesh with emphasis on Tiger (<i>Panthera tigris</i>). PhD dissertation. University of Dhaka.
  4. WWF. 2015. Saving forests at risk. WWF living forests report: Chapter 5. In: Taylor, R. (ed.), WWF living forests report. WWF, Gland.
  5. Gray, T.N.E., Thongsamouth, K. and Tilker, A. 2014b. Recent camera-trap records of Owston’s Civet <i>Chrotogale owstoni</i> and other small carnivores from Xe Sap National Protected Area, southern Lao PDR. <i>Small Carnivore Conservation</i> 51: 29–33.
  6. Gray, T.N.E., Pin C., Phan C., Crouthers, R., Kamler, J.F. and Prum S. 2014a. Camera-trap records of small carnivores from eastern Cambodia, 1999–2013. <i>Small Carnivore Conservation</i> 50: 20–24.
  7. Stibig, H.-J., Achard, F., Carboni, S., Raši, R. and Miettinen, J. 2014. Change in tropical forest cover of Southeast Asia from 1990 to 2010. <i>Biogeosciences</i> 11: 247–258.
  8. Rode-Margono, E.J., Voskamp, A., Spaan, D., Lehtinen, J.K., Roberts, P.D., Nijman, V. and Nekaris, K.A.I. 2014. Records of small carnivores and of medium-sized nocturnal mammals on Java, Indonesia. <i>Small Carnivore Conservation</i> 50: 1–11.
  9. Gaveau, D.L.A., Sloan, S., Molidena, E., Yaen, H., Sheil, D., Abram, N.K., Ancrenaz, M., Nasi, R., Quinones, M., Wielaard., N. and Meijaard, E. 2014. Four decades of forest persistence, clearance and logging on Borneo. <i>PLoS One</i> 9(7): e101654.
  10. Margono, B.A., Potapov, P.V., Turubanova, S.A., Stolle, F., Hansen, M.C. and Stole, F. 2014. Primary forest cover loss in Indonesia over 2000–2012. <i>Nature Climate Change</i> 4: 730–735.
  11. Willcox, D.H.A., Tran Q.P., Hoang M.D. and Nguyen T.T.A. 2014. The decline of non-<i>Panthera</i> cat species in Vietnam. <i>Cat News </i> Special Issue 8: 53–61.
  12. Chutipong, W., Tantipisanuh, N., Ngoprasert, D., Lynam, A.J., Steinmetz, R., Jenks, K.E., Grassman Jr., L.I., Tewes, M., Kitamura, S., Baker, M.C., McShea, W., Bhumpakphan, N., Sukmasuang, R., Gale, G.A., Harich, F.K., Treydte, A.C., Cutter, P., Cutter, P.B., Suwanrat, S., Siripattaranukul, K., Hala-Bala Wildlife Research Station, Wildlife Research Division and Duckworth, J.W. 2014. Current distribution and conservation status of small carnivores in Thailand: a baseline review. <i>Small Carnivore Conservation</i> 51: 96–136.
  13. Coudrat, C.N.Z., Nanthavong, C., Sayavong, S., Johnson, A., Johnston, J.B. and Robichaud, W.G. 2014. Conservation importance of Nakai-Nam Theun National Protected Area, Laos, for small carnivores based on camera trap data. <i>Raffles Bulletin of Zoology</i> 62: 31–49.
  14. WWF. 2013. Ecosystems in the Greater Mekong: Past Trends, Current Status, Possible Futures. WWF Greater Mekong Programme, [town not given].
  15. Naniwadekar, R., Shukla, U., Viswanathan, A. and Datta, A. 2013. Records of small carnivores from in and around Namdapha Tiger Reserve, Arunachal Pradesh, India. <i>Small Carnivore Conservation</i> 49: 1–8.
  16. Choudhury, A. 2013. <i>The mammals of North east India</i>. Gibbon Books and the Rhino Foundation for Nature in NE India, Guwahati, Assam, India.
  17. Murali, K.C., Kumar, A., Ray, P.C. and Sarma, K. 2013. Feeding observations of a Binturong <i>Arctictis binturong</i> group in Namdapha National Park, Arunachal Pradesh, India. <i>Small Carnivore Conservation</i> 49: 28–30.
  18. Samejima, H., Ong, R., Lagan, P. and Kitayama, K. 2012. Camera-trapping rates of mammals and birds in a Bornean tropical rainforest under sustainable forest management. <i>Forest Ecology and Management</i> 270: 248–256.
  19. Chua, M.A.H., Lim, K.K.P. and Low, C.H.S. 2012. The diversity and status of the civets (Viverridae) of Singapore. <i>Small Carnivore Conservation</i> 47: 1–10.
  20. Margono, B.A., Turubanova, S., Zhuravleva, I., Potapov, P., Tyukavina, A., Baccini, A., Goetz, S. and Hansen, M.C. 2012. Mapping and monitoring deforestation and forest degradation in Sumatra (Indonesia) using Landsat time series data sets from 1990 to 2010. <i>Environmental Research Letters</i> 7: 1-16.
  21. Miettinen, J., Shi, C. and Liew, S.C. 2011. Deforestation rates in insular Southeast Asia between 2000 and 2010. <i>Global Change Biology</i> 17(7): 2261-2270. DOI:10.111/j.1365-2486.2011.02398.x.
  22. Tempa, T., Norbu, N., Dhendup, P. and Nidup, T. 2011. Results from A Camera Trapping Exercise for Estimating Tiger Population Size in the Lower Foothills of Royal Manas National Park. UWICE and RMNP, Royal Government of Bhutan, Lamai Gompa, Bumtang, Bhutan.
  23. Low, C.H.S. 2011. Observations of civets, linsangs, mongooses and non-lutrine mustelids from Peninsular Malaysia. <i>Small Carnivore Conservation</i> 45: 8–13.
  24. Mathai, J., Hon, J., Juat, N., Peter, A. and Gumal, M. 2010. Small carnivores in a logging concession in the Upper Baram, Sarawak, Borneo. <i>Small Carnivore Conservation</i> 42: 1–9.
  25. Shepherd, C.R. and Shepherd, L.A. 2010. The trade in Viverridae and Prionodontidae in Peninsular Malaysia with notes on conservation and legislation. <i>Small Carnivore Conservation</i> 42: 27–29.
  26. Sodhi, N.S., Posa, M.R.C., Lee, T.M., Bickford, D., Koh, L.P. and Brook, B.W. 2010. The state and conservation of Southeast Asian biodiversity. <i>Biodiversity and Conservation</i> 19: 317-328.
  27. Lau, M.W.N., Fellowes, J.R. and Chan, B.P.L. 2010. Carnivores (Mammalia: Carnivora) in South China: a status review with notes on the commercial trade. <i>Mammal Review</i> 42: 247–292.
  28. Johnson, A., Vongkhamheng, C. and Saithongdam, T. 2009. The diversity, status and conservation of small carnivores in a montane tropical forest in northern Laos. <i>Oryx</i> 43: 626–633.
  29. Shepherd, C.R. 2008. Civets in trade in Medan, North Sumatra, Indonesia (1997-2001) with notes on legal protection. <i>Small Carnivore Conservation</i> 38: 34–36.
  30. Meijaard, E., Sheil, D., Marshall, A.J. and Nasi, R. 2008. Phylogenetic age is positively correlated with sensitivity to timber harvest in Bornean mammals. <i>Biotropica</i> 40: 76–85.
Évaluateurs & contributeurs (3)Expert
assessor
Willcox, D.H.A., Chutipong, W., Gray, T.N.E., Cheyne, S., Semiadi, G., Rahman, H., Coudrat, C.N.Z., Jennings, A., Ghimirey, Y., Ross, J., Fredriksson, G. & Tilker, A.
contributor
Holden, J., Choudhury, A., Thapa, S., Widmann, P. & de Leon, J.
evaluator
Duckworth, J.W.

Willcox, D.H.A., Chutipong, W., Gray, T.N.E., Cheyne, S., Semiadi, G., Rahman, H., Coudrat, C.N.Z., Jennings, A., Ghimirey, Y., Ross, J., Fredriksson, G. & Tilker, A. 2016. Arctictis binturong. The IUCN Red List of Threatened Species 2016: e.T41690A45217088. Accessed on 05 May 2026.

Traits biologiques

23 valeurs · 8 sources

Morphologie(5)

Masse adulte
14 kg
AnAge
Masse cerveau
42 g
AnimalTraits
Masse naissance
318 g
AnAge
Masse au sevrage
2,1 kg
AnAge
Longueur
78,5 cm
PanTHERIA

Cycle de vie(1)

Longévité max
27 ans
AnAge
Voir 17 traits de plus (3 catégories)

Reproduction(6)

Sevrage
2,6 mois
AnAge
Taille de portée
2
AnAge
Maturité sexuelle
2,3 ans
AnAge
Portées par an
2
AnAge
Gestation
3 mois
AnAge
Intervalle naissances
11,4 mois
AnAge

Écologie & habitat(9)

Invertébrés (%)
0 %
elton_mammals
Graines (%)
0 %
elton_mammals
Fruits (%)
30 %
elton_mammals
Nectar (%)
0 %
elton_mammals
Charognard (%)
10 %
elton_mammals
Poissons (%)
30 %
elton_mammals
Autre végétal (%)
20 %
elton_mammals
Vert. ectothermes (%)
0 %
elton_mammals
Vert. endothermes (%)
10 %
elton_mammals

Divers(2)

Taux métabolique
12.75 W
AnAge
Température corporelle
36,7 °C
AnAge

Sources priorisées par qualité scientifique (peer-reviewed spécialisées → Wikidata fallback). Unités auto-converties, valeur max retenue en cas de mesures multiples. Méthodologie · Citations.

Répartition mondiale

Aucune observation géoréférencée avec précision suffisante (<10 km) dans GBIF pour cette espèce.

Consulter sur les bases externes

Observations & statuts

Cartographie

Bibliographie

Note nomenclaturale & synonymesExpert

Note nomenclaturale

TAXREF v18 — INPN/MNHN

Synonymes (1)— redirigent vers cette page

  • Viverra binturongRaffles, 1822

Sources : Catalogue of Life Cross-References (synonymes) · TAXREF v18 INPN/MNHN (commentaires FR).