Ontologia

Chien Des Buissons

Speothos venaticus(Lund, 1842)

NTLR Monde (IUCN)
  1. Animal
  2. Chordata
  3. Mammalia
  4. Carnivora
  5. Canidae
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 Speothos venaticus 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

28 partenaires écologiques documentés directement dans GloBI.

Partenaires
28
Espèces avec interactions documentées
Types d'interactions
7
Prédation, pollinisation, parasitisme…
Connectance
0.067
Densité des liens dans le sous-graphe affiché
Rang animalia
89 %
Percentile vs ensemble des animalia

Liste rouge IUCN

NT · Quasi menacéeDécroissante
Évaluation complète
Évaluation
2011 · v3.1
Altitude
1500 m
Profondeur
m
État de la populationExpert

Despite its large distributional range and occurrence in a variety of habitats, Bush Dogs seem to be naturally rare throughout their range. In a recent survey by DeMatteo (2008), the majority of countries in the Bush Dog’s distribution reported the status of the species as rare or unknown  (rare: Ecuador; rare or unknown: Argentina, Bolivia, Brazil, French Guiana, Paraguay; unknown: Panama and Venezuela) and only two countries reported it as common (Guyana and Peru). The species is seldom recorded with camera traps; however, caution should be taken when interpreting the lack of detection, as this may actually be associated with the species actively avoiding features associated with this technique (e.g., placement of traps along animal trails used by other carnivores) or assumptions on animal movement (e.g., placement along roads assumes the animal will walk along the road versus cross over the road).

Demographic data for Bush Dogs are lacking throughout their range and population estimates have been reported only for a few areas: <100 in Misiones Argentina (DeMatteo 2008), >1,000 in Bolivia (DeMatteo 2008), > 1,000 in 4,022 km² or one individual/4 km² in Cusco Peru within the Camisea River region (DeMatteo 2008), 0.04 individuals/km² (B. Beisiegel pers. comm.) in Brazil, 0.025 individuals/km² in partially fragmented cerrado in Mato Grosso Brazil (E.S. Lima, K.E. DeMatteo, R.S.P. Jorge, M.L.S.P. Jorge, J. Dalponte, H.S. Lima, and S. Klorfine, pers. obs.), 15.8 individuals/394 km² or 0.04 individuals/km² in the Pantanal in Brazil (Lima, Jorge et al. 2009), and 0.001 individuals/km² in fragmented southern Amazonia Brazil (Michalski 2010). A suitable area of approximately 11,000,000km² (DeMatteo and Loiselle 2008), and an average population density of ca. 0.01 individuals/km², would predict an estimated population of 110,000 individuals, approximately half of which would be mature; however, the effects of fragmentation, degree of protection, and variability across their broad distribution would suggest that this is an over-estimate.

Across the Bush Dog’s distribution, population trends are reported as unknown in two countries (Guyana and Panama), declining in two (Paraguay and Venezuela), unknown or stable in one (French Guiana), and stable in two (Ecuador and Peru, specifically Cusco Peru) (DeMatteo 2008). Across the entire range, increasing levels of habitat fragmentation (urbanization and agriculture), threats to prey populations with illegal poaching, and exposure to potentially lethal candid-related diseases, mean that the probability that the trend is stable or increasing is highly unlikely.

Menaces identifiées(13 menaces classées CMP-IUCN)

  • 1_1
    Housing & urban areas
    Ongoing
  • 2_1_3
    Agro-industry farming
    Ongoing
  • 2_2_2
    Agro-industry plantations
    Ongoing
  • 2_3_2
    Small-holder grazing, ranching or farming
    Ongoing
  • 2_3_3
    Agro-industry grazing, ranching or farming
    Ongoing
  • 5_1_2
    Unintentional effects (species is not the target)
    Ongoing
  • 8_1_1
    Unspecified species
    Ongoing
  • 8_1_2
    Named species
    Ongoing
  • 8_1_2
    Named species
    Ongoing
  • 8_1_2
    Named species
    Ongoing

+ 3 menaces supplémentaires

Description complète des menacesExpert

There are several serious perceived threats, including: 1) human encroachment and loss of intact habitat due to large-scale agriculture (e.g., soybean), conversion of land to pasture, and large-scale plantations of monoculture trees (e.g., eucalyptus, pine); 2) reduction in prey abundance due to illegal poaching and domestic dog predation; and 3) increased risk of contracting lethal diseases from domestic dogs (proximity to human populations and hunting dogs (DeMatteo 2008).

Canid-related diseases are a threat not previously identified for Bush Dogs. However, field evidence supports that pathogens may be transmitted by domestic dogs, and the effects can be potentially devastating, mainly due to the species’ group living (Mann et al. 1980, Steinel et al. 2001, Leite Pitman, Nieto et al. 2003, Jorge, Morato et al. 2007, Jorge, Nunes, et al. 2007, DeMatteo 2008, Jorge et al. 2008, E.S. Lima, K.E. DeMatteo, R.S.P. Jorge, M.L.S.P. Jorge, J. Dalponte, H.S. Lima, and S. Klorfine, pers. obs.). E.S. Lima, K.E. DeMatteo, R.S.P. Jorge, M.L.S.P. Jorge, J. Dalponte, H.S. Lima, and S. Klorfine (pers. obs.) observed this effect when a generalized hair loss, suspected to be a type of mange, gradually spread through a group of wild Bush Dogs, eventually killing all individuals. In addition to mange, parvovirus and rabies are diseases reported as negatively effecting wild populations (Mann et al. 1980, DeMatteo 2008).  The species has been identified to be susceptible to both Dioctophyma renale and Amphimerus interruptus (museum collections - Vierira et al. 2008), Lagochilascaris sp. (Volcán and Medrano 1991), and as a host for Echinococcus vogeli (Cestoda: Taeniidae) (Rausch and Bernstein 1972). Captive animals have been identified as susceptible to a variety of diseases and parasites, including parvovirus (Janssen et al. 1982), vaccine-induced canine distemper (McInnes et al. 1992), leishmania (Lima, Fattori et al. 2009), Spirocerca lupi (Rinas et al. 2009), Toxoplasma gondii (Sedlak and Bartova 2006), and Campylobacter (L. Saboia pers. comm.). With the latter, 13 of 15 individuals in a large family group suddenly died from severe haemorrhagic enteritis when they contracted Campylobacter from an infected Coati that they were inadvertently fed (L. Saboia pers. comm.). This loss of multiple animals in a short period emphasizes both the species sensitivity to various diseases and the susceptibility of group living species to pathogens. With increasing proximity to human areas and intrusion into protected areas with hunting dogs, the risk of exposure to disease is potentially high. Exposure to disease may also result from feral or semi-feral, non-vaccinated, domestic dogs that regularly hunt prey independent of humans (K. DeMatteo pers. obs.). DeMatteo (2008) noted that in Brazil more problem interactions were noted to occur between Bush Dogs and domestic dogs than with livestock, which only emphasizes the threat of disease to the species.  

Habitats préférentiels (classification IUCN)

  • 14_2Artificial/Terrestrial - Pastureland
  • 1_5Forest - Subtropical/Tropical Dry
  • 1_6Forest - Subtropical/Tropical Moist Lowland
  • 1_8Forest - Subtropical/Tropical Swamp
  • 1_9Forest - Subtropical/Tropical Moist Montane
  • 2_1Savanna - Dry
  • 2_2Savanna - Moist
  • 3_5Shrubland - Subtropical/Tropical Dry
  • 4_4Grassland - Temperate
Mesures de conservation recommandéesExpert

This species occurs in several protected areas throughout its range, but it has a patchy distribution and occurs at very low densities. Hunting is prohibited in Colombia (Law Number 848:1973), Ecuador (Law Number 74:1981), French Guiana (Law Number JO19860625:1986), Panama (Law Number 2-80:1980), Paraguay (Law Number 18796:1975) and Peru (Law Number 5056:1970). Hunting and trade is regulated in Argentina (Law Number 22.421:1981), Bolivia (Law Number 12301:1975), Brazil (Law Number 5197:191967), and Venezuela (Law Number 276:1970). There is no Information for Guyana and Suriname. Unfortunately, in many parts of its range, resources are inadequate to manage designated protected areas and enforce existing wildlife laws.

Included in CITES on Appendix I.

Bush Dogs occur in captivity and are part of a successful international breeding programme (Buck 2009), which includes Asia (Japan), Europe, Brazil, and North America. There have been no known attempts at reintroduction.

Population estimates and demographic data for Bush Dogs is still little known across its range. This extends to an understanding of the social dynamics of individual groups, especially in terms of dispersal of young and area of use relative to other groups (overlapping or separate home ranges). Habitat associations are not clearly understood – the species was once thought to be dependent on forests but is now increasingly observed in open and fragmented habitats; however there is no data on population viability in such areas. While preliminary data on diet supports a primarily carnivorous diet, seasonal changes and geographical variation in diet needs to be evaluated. Determining how the impact of disease, especially transmission dynamics from domestic dogs, can be managed or minimized in wild populations needs to be addressed. Interspecific relationships with sympatric carnivores needs to be further evaluated.

Locating evidence of species presence using standard survey techniques, including camera traps and transect surveys, has proven difficult (Beisiegel 2009, DeMatteo et al. 2009, Michalski 2010). The use of artificial scent lures, which can increase attraction to a specific location, have been unsuccessful with wild Bush Dogs (Zuercher et al. 1999). However, there are several methodological adjustments that may increase the effectiveness of these techniques with the species, including adjusting the height of camera placement, increasing trapping effort, and concurrent use of long-call vocalization playbacks and conspecific urine (DeMatteo et al. 2004). Limited field trials in partially fragmented cerrado (2004-2005) with playbacks, urine, and leg-hold traps were unsuccessful (K. DeMatteo unpubl. data). However, additional trials are needed to determine how species density, habitat variability (forest versus cerrado), and prey density alters technique effectiveness. 

Preliminary and ongoing research using a combination of three non-invasive techniques (scent-detection dogs, faecal DNA screening, GIS technology) has been shown to be successful for the species (DeMatteo et al. 2009, unpubl. data) and should be expanded to additional regions and habitat. This suite of techniques eliminates the need to attract the species to a specific location and allows insight into many ecological variables including habitat use (intact and fragmented), population status, minimum area of use, and niche overlap/separation with other carnivores.

Actions de conservation (3)Expert
  • 2_1Site/area management
  • 2_2Invasive/problematic species control
  • 5_4_2National level
Stress écologiques (25)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
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_3_7Reduced reproductive success
  • 2_3_8Other
Usage & commerce (2)Expert
  • 1Food - human
    subsistance
  • 15Sport hunting/specimen collecting
    subsistance
Priorités de recherche (2)Expert
  • 1_2Population size, distribution & trends
  • 1_3Life history & ecology
Niche IUCN globaleExpert

Royaumes biogéographiques

Neotropical

Systèmes (terrestre/eau douce/marin)

Terrestrial
Références bibliographiques (30)Expert
  1. IUCN. 2011. IUCN Red List of Threatened Species (ver. 2011.2). Available at: <a href="http://www.iucnredlist.org">http://www.iucnredlist.org</a>. (Accessed: 10 November 2011).
  2. Michalski, F. 2010. The bush dog Speothos venaticus and short-eared dog Atelocynus microtis in a fragmented landscape in southern Amazonia. <i>Oryx</i> 44: 300-303.
  3. Beisiegel, B. M. 2009. First camera trap record of bush dogs in the state of São Paulo, Brazil. <i>Canid News</i> 12.5.
  4. Lima, E. S., Jorge, R. S. P. and Dalponte, J. C. 2009. Habitat use and diet of bush dogs, Speothos venaticus, in the Northern Pantanal, Mato Grosso Brazil. <i>Mammalia</i> 73: 13-19.
  5. Oliveira, T. G. 2009. Distribution, habitat utilization and conservation of the Vulnerable bush dog Speothos venaticus in northern Brazil. <i>Oryx</i> 43: 247-253.
  6. Buck, N. 2009. <i>International Studbook for the bush dog Speothos venaticus (Lund, 1842).</i> The Aspinall Wild Animal Experience/World Association of Zoos and Aquariums (WAZA), Port Lympne.
  7. DeMatteo, K. E., Rinas, M. A., Sede, M. M., Davenport, B., Argüelles, C., Lovett, K. and Parker, P.G. 2009. Detector dogs: an effective technique for bush dog (Speothos venaticus) surveys. <i>Journal of Wildlife Management</i> 73: 1436-1440.
  8. Lima, V. M. F., Fattori, K. R., Michelin, A. de F., Nogueira, F. S. and Souza, L. de O. 2009. Evidence of Leishmania spp. Antibodies and DNA in bush dogs (Speothos venaticus) in Brazil. <i>Journal of Wildlife Medicine</i> 40: 91-94.
  9. Rinas, M. A., Nesnek, R., Kinsella, M. and DeMatteo, K. E. 2009. Fatal aortic aneurysm and rupture in a neotropical bush dog (Speothos venaticus) cause by Spirocerca lupi. <i>Veterinary Parasitology</i> 164: 347-349.
  10. Vierira, F.M., Luque, J.L., and Muniz-Pereira, L.C. 2008. Checklist of helminth parasites in wild carnivore mammals from Brazil. <i>Zootaxa</i> 1721: 1-23.
  11. DeMatteo, K. E. 2008. Using a survey of carnivore conservationists to gain insight into the ecology and conservation status of the bush dog. <i>Canid News</i> 11.3.
  12. DeMatteo, K. E. and Loiselle, B. A. 2008. New data on the status and distribution of the bush dog (Speothos venaticus): evaluating its quality of protection and directing research efforts. <i>Biological Conservation</i> 141: 2494-2505.
  13. Jorge, R. S. P., Nunes, C. M., Trinconi, C. M., Paula, H. B., Dias, A. K. K. and Ferreira, F. 2007. Leishmania spp. in wild carnivores captured in the Pantanal, Brazil. 56th Annual Wildlife Disease Association Conference: 42. Estes Park, Colorado.
  14. Jorge, R. S. P., Morato, R. G., Pereira, M., Lima, E. S., Scheffer, K., Carnieli Jr., P., Kotait, I. and Ferreira, F. 2007. Rabies antibodies in a bush dog captured in the Pantanal, Brazil. 56th Annual Wildlife Disease Association Conference: 94. Estes Park, Colorado.
  15. Sedlak, K. And Bartova, E. 2006. Seroprevalences of antibodies to Neospora caninum and Toxoplasma gondii in zoo animals. <i>Veterinary Parasitology</i> 136: 223-231.
  16. Zuercher, G. L., Gipson, P. S. and Carrillo, O. 2005. Diet and habitat associations of bush dogs Speothos venaticus in the Interior Atlantic Forest of eastern Paraguay. <i>Oryx</i> 39: 86-89.
  17. Beisiegel, B. M. and Zuercher, G.L. 2005. Speothos venaticus. <i>Mammalian Species 783: 1-6</i> 783: 1-6.
  18. Michalski, F. and Peres, C. A. 2005. Anthropogenic determinants of primate and carnivore local extinctions in a fragmented forest landscape of southern Amazonia. <i>Biological Conservation</i> 124: 383-396.
  19. Beisiegel, B. M. and Ades, C. 2004. The bush dog <i>Speothos venaticus</i> (Lund, 1842) at Parque Estadual Carlos Botelho, Southeastern Brazil. <i>Mammalia</i> 68: 65-68.
  20. DeMatteo, K. E., Carrillo, O., Zuercher, G. L., Ramírez, S., Smith, K. and Porton, I. J. 2004. A technique for attracting bush dogs (Speothos venaticus) in the wild. <i>Canid News</i> 7.6: 1-12.
  21. Sillero-Zubiri, C., Hoffmann, M. and Macdonald, D.W. (eds). 2004. <i>Canids: Foxes, Wolves, Jackals and Dogs. Status Survey and Conservation Action Plan</i>. IUCN/SSC Canid Specialist Group, IUCN, Gland, Switzerland and Cambridge, UK.
  22. Leite Pitman, M.R.P., Nieto, F.V. and Davenport, L. 2003. Amenaza de enfermedades epidémicas a la conservación de carnívoros silvestres en la Amazonía peruan. In: M.R.P. Leite Pitman, N.C.A. Pitman and P.C. Alvarez (eds), <i>Alto Purús: Biodiversidad, Conservación y Manejo</i>, pp. 227-231. Center for Tropical Conservation and INRENA.
  23. Leite Pitman, M.R.P., Beck, H. and Velazco, P. 2003. Mamíferos terrestres y arbóreos de la selva baja de la Amazonía peruana entre los ríos Manu y Alto Purú. In: M.R.P. Leite Pitman, N.C.A. Pitman and P.C. Alvarez (eds), <i>Alto Purús: Biodiversidad, Conservación y Manejo</i>, pp. 109-122. Center for Tropical Conservation and INRENA.
  24. Zuercher, G. L. and Villalba, R. D. 2002. Records of <i>Speothos venaticus</i> Lund, 1842 (Carnivora, Canidae) in eastern Paraguay. <i>Mammalian Biology</i> 67: 185-187.
  25. Steinel A., Parrish, C.R., Bloom, M.E., Truyen, U. 2001. Parvovirus Infections in Wild Carnivores. <i>Journal of Wildlife Diseases</i> 37: 594-607.
  26. de la Rosa, C.L. and Nocke, C.C. 2000. <i>A Guide to the Carnivores of Central America: Natural History, Ecology, and Conservation</i>. University of Texas Press, Austin, TX, USA.
  27. Farias, V. 2000. Gray fox distribution in southern California: detecting the effects of intraguild predation. M.Sc. Thesis, University of Massachusetts.
  28. Beisiegel, B. M. 1999. Contribuição ao estudo da história natural do cachorro do mato, Cerdocyon thous, e do cachorro vinagre, Speothos venaticus. Instituto de Psicologia, Universidade de São Paulo.
  29. Silveira, L., Jácomo, A. T. A., Rodrigues, F. H. G. and Diniz-Filho, J. A. F. 1998. Bush dogs (<i>Speothos venaticus</i>), in Emas National Park, Central Brazil. <i>Mammalia</i> 62: 446-449.
  30. Emmons, L. H. 1998. Mammal fauna of Parque Nacional Noel Kempff Mercado. In: T. Killeen and T. Schulemberg (eds), <i>A biological assesment of Parque Nacional Noel Kempff Mercado, Bolivia, RAP Working Papers 10</i>, pp. 129-135. Conservation International, Washington, DC, USA.
Évaluateurs & contributeurs (3)Expert
assessor
DeMatteo, K., Michalski , F. & Leite-Pitman, M.R.P.
contributor
Zuercher , G., Swarner, M., Silveira, L. & Carrillo, O.
evaluator
Sillero-Zubiri, C. & Hoffmann, M.

DeMatteo, K., Michalski , F. & Leite-Pitman, M.R.P. 2011. Speothos venaticus. The IUCN Red List of Threatened Species 2011: e.T20468A9203243. Accessed on 05 May 2026.

Traits biologiques

20 valeurs · 6 sources

Morphologie(4)

Masse adulte
6 kg
AnAge
Masse naissance
160 g
AnAge
Longueur
62,5 cm
PanTHERIA
Masse au sevrage
-999000 mg
PanTHERIA

Cycle de vie(1)

Longévité max
14 ans
AnAge
Voir 15 traits de plus (2 catégories)

Reproduction(6)

Sevrage
3,3 mois
AnAge
Taille de portée
4
AnAge
Maturité sexuelle
1 ans
AnAge
Portées par an
2
AnAge
Gestation
2,2 mois
AnAge
Intervalle naissances
8,2 mois
AnAge

Écologie & habitat(9)

Invertébrés (%)
0 %
elton_mammals
Graines (%)
0 %
elton_mammals
Fruits (%)
0 %
elton_mammals
Nectar (%)
0 %
elton_mammals
Charognard (%)
0 %
elton_mammals
Poissons (%)
0 %
elton_mammals
Autre végétal (%)
0 %
elton_mammals
Vert. ectothermes (%)
0 %
elton_mammals
Vert. endothermes (%)
100 %
elton_mammals

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

Bibliographie

Note nomenclaturale & synonymesExpert

Note nomenclaturale

TAXREF v18 — INPN/MNHN

Synonymes (1)— redirigent vers cette page

  • Cynogale venaticaLund, 1842

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