
Balisaur
Arctonyx collarisF. G. Cuvier, 1825
Description
espèce de mammifères
Source : Wikidata
Indicateurs du réseau écologique
Comment lire ce graphe
Ce graphe représente les interactions écologiques documentées entre Arctonyx collaris 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
11 partenaires écologiques documentés directement dans GloBI.
Liste rouge IUCN
VU · Vulnérablecritères A2cd+3cd+4cd↘Décroissante- Évaluation
- 2024 · v3.1
- Altitude
- 0 – 2300 m
- Profondeur
- – m
État de la populationTexte officiel évaluation IUCNExpert
At least two factors might produce this heterogeneous recording pattern: (i) natural variation in densities and (ii) human-induced declines proceeding at different rates across the range. Both are probably important. Past information is rarely precise enough to assess even the coarse population trend directly. However, judging by patterns in better documented hunting-sensitive groups of ground-dwelling mammals (e.g., wild cattle Bos, Leopard Panthera pardus, Sambar Rusa unicolor), it would be reasonable to expect human pressure to have depressed densities in Lao PDR and Viet Nam more than in Thailand and Cambodia. And this indeed seems to have happened. Recent camera-trapping has recorded the species in only very few areas in Viet Nam (Willcox et al. 2014: Table SOM3, Nguyen T. pers. comm. 2014); Roberton (2007) had already drawn attention to the surprising paucity of records in the country in the 1990s and early 2000s. In Lao PDR, by contrast, all published large-scale camera-trap surveys have found the species (Nam Et–Phou Louey NPA, Johnson et al. 2009; Nakai–Nam Theun NPA, Coudrat et al. 2014; Xe Sap NPA, Gray et al. 2014b), indicating a healthier status than in Vietnam (as is typical for hunting-sensitive species). The three camera-trap survey areas are likely to hold amongst the least-depleted large mammal faunas in Lao PDR. All are in rugged mountainous areas and indeed all post-1990 Lao records of Hog Badger come from hill and montane areas; there has been none from the plains. This pattern, making due allowance for the distribution of survey effort, was already apparent in the pre-camera-trapping era by 1999, based on direct sightings and records of dead animals or their parts (Duckworth et al. 1999). By contrast, this species is commonly recorded at low altitudes, including in plains landscapes, of Thailand and Cambodia (Royan 2010, Gray et al. 2014a, Chutipong et al. 2014) and it is common in similar lowland terrain in Kaziranga NP, Assam (Choudhury 2013). This suggests strongly that the absence of recent Lao records from such terrain (where hunting is more efficient than in rugged terrain, meaning that hunting-sensitive species across a range of vertebrate taxa tend to have declined faster there) reflects steep declines (and plausibly widespread extirpation) there.
The occurrence in Myanmar is also patchy without obvious natural explanation (Than Zaw et al. 2008); thus far, the pattern of records has not been compared closely with those of species known to be sensitive to hunting. In Cambodia, while it has been recorded relatively commonly in some areas such as parts of the north-east (Gray et al. 2014a), in the 'northern plains', west of the Mekong, it was not recorded in 6,000 camera-trap nights of survey in the 2012-2013 and 2013–2014 dry seasons, and the most recent record there seems to have been in 2001 (D. H. A. Willcox pers. comm. 2014). Thus area abuts Lao PDR and this apparent range retreat corroborates the suggestion that it has been hunted out from such habitat in Lao PDR. In Thailand, it seems to remain generally common with no large landscapes of (semi-) natural habitat lacking records (when patterns in survey effort are allowed for) (Chutipong et al. 2014). In North-east India the genus, although widespread, is generally not common (Choudhury 2013). The population status in its Chinese range (part of Yunnan province) seems poorly known, even at the level of genus.
Menaces identifiées(17 menaces classées CMP-IUCN)
5_1_1Intentional use (species is the target)Rapid DeclinesMajority (50-90%)Ongoing5_1_2Unintentional effects (species is not the target)Rapid DeclinesMajority (50-90%)Ongoing1_1Housing & urban areasNegligible declinesMinority (<50%)Ongoing1_2Commercial & industrial areasNegligible declinesMinority (<50%)Ongoing2_1_1Shifting agricultureSlow, Significant DeclinesMajority (50-90%)Ongoing2_1_2Small-holder farmingSlow, Significant DeclinesMajority (50-90%)Ongoing2_1_3Agro-industry farmingSlow, Significant DeclinesMajority (50-90%)Ongoing2_2_1Small-holder plantationsSlow, Significant DeclinesMajority (50-90%)Ongoing2_2_2Agro-industry plantationsSlow, Significant DeclinesMinority (<50%)Ongoing3_2Mining & quarryingSlow, Significant DeclinesMinority (<50%)Ongoing
+ 7 menaces supplémentaires
Description complète des menacesTexte détaillé évaluation IUCNExpert
The threat which habitat change poses directly to this species is not clear. Indirectly, anything that opens up access to areas previously difficult to enter, in particular which allows vehicular removal of wildlife for sale, exacerbates the hunting threat. Almost all forms of habitat change by people co-occur with increased human access and presence, making the indirect threat from habitat change severe. Based on localities of specific records, it is unlikely that degraded and fragmented natural habitat are inherently unsuitable. These are not widely occupied probably because their higher densities of people, with concomitantly increased likelihood for badgers of lethal incidental encounters with people, prevent this. Outright conversion to entirely artificial habitat (agriculture, settlement and infrastructure) seems more likely to render an area unsuitable for Greater Hog Badger, but even this remains to be proven. Overall, the existence of large tracts of forest in the eastern parts of the species's range with at best low densities of this species indicate that there the chief threat is hunting. While perhaps this is not yet so in parts of the western range, it is increasingly likely to become so there, too.
In Kaziranga National Park, India, numbers die in the periodic inundation of this flood-plain (Choudhury 2013). While formerly such animals might have been able to move safely to higher ground, the increasing fragmentation of natural habitat probably leads to higher mortalities nowadays. Nonetheless, in total these are likely to be insignificant to overall decline rates of the species, and are only a potential threat at the most local of levels.
Hog badger hairs are used in European shaving brush manufacture (Domingo-Roura et al. 2006) but whether this species and wild populations are involved is unclear; the large farmed stock in China (Lau et al. 2010) seems a more likely origin.
Habitats préférentiels (classification IUCN)
1_6Forest - Subtropical/Tropical Moist Lowland★1_9Forest - Subtropical/Tropical Moist Montane★4_6Grassland - Subtropical/Tropical Seasonally Wet/Flooded★1_5Forest - Subtropical/Tropical Dry2_1Savanna - Dry2_2Savanna - Moist3_5Shrubland - Subtropical/Tropical Dry3_6Shrubland - Subtropical/Tropical Moist4_5Grassland - Subtropical/Tropical Dry14_6Artificial/Terrestrial - Subtropical/Tropical Heavily Degraded Former Forest
Mesures de conservation recommandéesStratégies de conservation IUCNExpert
Actions de conservation (8)Conservation Actions Classification Scheme — IUCNExpert
2_1Site/area management5_1_1International level5_1_2National level5_1_3Sub-national level5_2Policies and regulations5_4_1International level5_4_2National level5_4_3Sub-national level
Stress écologiques (26)Stresses Classification — IUCNExpert
1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation2_1Species mortality2_1Species mortality
Usage & commerce (2)Use & Trade — IUCNExpert
1Food - humansubsistance16Establishing ex-situ production *
Priorités de recherche (8)Research Needed Classification — IUCNExpert
1_2Population size, distribution & trends1_3Life history & ecology1_4Harvest, use & livelihoods1_5Threats1_6Actions3_1Population trends3_2Harvest level trends3_3Trade trends
Niche IUCN globaleRealms · Systems · LMEs · Growth forms · FAOs — biogéographie IUCNExpert
Royaumes biogéographiques
Systèmes (terrestre/eau douce/marin)
Références bibliographiques (23)Sources scientifiques de l'évaluation IUCNExpert
- IUCN. 2024. The IUCN Red List of Threatened Species. Version 2024-2. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 28 October 2024).
- 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).
- Gray, T.N.E., Thongsamouth, K. and Tilker, A. 2014b. Recent cameratrap 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- Feeroz, M.M., Hasan, M.K. and Hossain, M.K. 2012. <i>Biodiversity of protected areas of Bangladesh, Vol. 2: Dudpukuria-Dhopacharia Wildlife Sanctuary</i>. Bio Track. Arannayak Foundation, Dhaka, Bangladesh.
- 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.
- Royan, A. 2010. Significant mammal records from Botum–Sakor National Park, southwest Cambodia. <i>Cambodian Journal of Natural History</i> '2010’(1): 22–26.
- Holden, J. and Neang T. 2009. Small carnivore records from the Cardamom Mountains, southwestern Cambodia. <i>Small Carnivore Conservation</i> 40: 16–21.
- 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.
- Than Zaw, Saw Htun, Saw Htoo Tha Po, Myint Maung, Lynam, A.J., Kyaw Thinn Latt and Duckworth, J.W. 2008. Status and distribution of small carnivores in Myanmar. <i>Small Carnivore Conservation</i> 38: 2–28.
- Helgen, K.M., Lim, N.T-L. and Helgen, L.E. 2008. The hog-badger is not an edentate: systematics and evolution of the genus <i>Arctonyx</i> (Mammalia: Mustelidae). <i>Zoological Journal of the Linnean Society</i> 154: 353–385.
- Roberton, S.I. 2007. Status and conservation of small carnivores in Vietnam. University of East Anglia, Norwich, U.K. (Ph.D. thesis).
- Domingo-Roura, X., Marmi, J., Ferrando, A., López-Giráldez, J.F., Macdonald, D.W., Jansman, H.A.H. 2006. Badger hair in shaving brushes comes from protected Eurasian badgers. <i>Biological Conservation</i> 128: 425–430.
- SFNC. 2000. <i>Pù Mát: a biodiversity survey of a Vietnamese protected area</i>. SFNC Project, Vinh, Vietnam.
- Duckworth, J.W., Salter, R.E. and Khounboline, K. 1999. Wildlife in Lao PDR: 1999 Status Report. IUCN, Vientiane, Laos.
- Timmins, R.J., Do Tuoc, Trinh Viet Cuong and Hendrichsen, D.K. 1999. A preliminary assessment of the conservation importance and conservation priorities of the Phong Nha-Ke Bang proposed National Park, Quang Binh Province, Vietnam. Fauna and Flora International-Indochina Programme, Hanoi, Vietnam.
- Timmins, R.J. and Duckworth, J.W. 1999. Status and conservation of Douc Langurs (<i>Pygathrix nemaeus</i>) in Laos. <i>International Journal of Primatology</i> 20: 469 – 489.
- Duckworth, J.W. 1997. Small carnivores in Laos: a status review with notes on ecology, behaviour and conservation. <i>Small Carnivore Conservation</i> 16: 1–21.
- Pocock, R.I. 1941. <i>The Fauna of British India, including Ceylon and Burma</i>. Taylor & Francis, Ltd., London, UK.
Évaluateurs & contributeurs (3)Personnes ayant contribué à l'évaluation IUCNExpert
Duckworth, J.W., Timmins, R.J., Chutipong, W., Gray, T.N.E., Long, B., Helgen, K., Rahman, H., Choudhury, A.U. & Willcox, D.H.A. 2024. Arctonyx collaris (amended version of 2016 assessment). The IUCN Red List of Threatened Species 2024: e.T70205537A259343689. Accessed on 05 May 2026.
Traits biologiques
Morphologie(4)
Cycle de vie(1)
Voir 15 traits de plus (2 catégories)Replier
Reproduction(6)
Écologie & habitat(9)
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
Note nomenclaturale & synonymesDétails taxonomiques + synonymes CoLExpert
Note nomenclaturale
TAXREF v18 — INPN/MNHNSynonymes (6)— redirigent vers cette page
- Arctonyx annaeusThomas, 1921
- Arctonyx collaris collarisF. G. Cuvier, 1825
- Arctonyx collaris consulPocock, 1940
- Arctonyx collaris dictatorThomas, 1910
- Arctonyx collaris nemaeusPocock, 1941
- Arctonyx dictatorThomas, 1910
Sources : Catalogue of Life Cross-References (synonymes) · TAXREF v18 INPN/MNHN (commentaires FR).