Ontologia
Renard de Darwin

Renard de Darwin

Lycalopex fulvipes(Martin, 1837)

ENLR Monde (IUCN)
  1. Animal
  2. Chordata
  3. Mammalia
  4. Carnivora
  5. Canidae
1 photo · Licences CC (Wikimedia Commons / iNaturalist)Click pour agrandir

Description

espèce de mammifères

Source : Wikidata

Pays · région · aire protégée · écorégion · biome

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Calcul du tissu écologique de Lycalopex fulvipes.

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Liste rouge IUCN

EN · En dangercritères C1Décroissante
Évaluation complète
Évaluation
2016 · v3.1
Altitude
01400 m
Profondeur
m
État de la populationExpert

In Ahuenco, Chiloé, Jiménez (2007) estimated a density of 0.92 foxes/km² in an area that seems to be prime for the species. In Nahuelbuta, D. Moreira et al. (pers. obs.) have recently found that foxes are patchily distributed across the landscape reaching densities of c. 0.75 foxes/km² in areas with less disturbed native forest. Foxes are described as common in Chiloé, except for the northern and eastern areas of the island (Jiménez and McMahon 2004). The presence of foxes seems to be largely explained by native forest (Moreira-Arce et al. 2015a). Farías and Jaksic (2011) report for north-eastern Chiloé (likely among the less suitable area for foxes in the island, Jiménez and McMahon 2004) that occupancy was associated with fragment size, with larger fragments mostly occupied. Moreira-Arce et al. (2015a) report occupancy of 32% for Nahuelbuta (around 10% of cameras with detections). Preliminary data from the Valdivian Coastal Reserve and Alerce Costero National Park (E. A. Silva-Rodríguez et al. pers. obs., A. Farías and Svensson pers. obs.) suggests similar detection rates than for Nahuelbuta. Genetic variability is extremely low for both populations, and despite its presumed larger population size, is lower in Chiloé than in mainland (J. Cabello et al. pers. obs.). Polymorphism in animals from Chiloé is lower than in other species (Cabello and Dávila 2014).

Jiménez and McMahon (2004) estimated that the extant Darwin’s Fox population was 78 individuals for Nahuelbuta National Park (and less than 100 for the Nahuelbuta range) and around 500 in Chiloé. For the purpose of this account a conservative approach was used to obtain an educated guess of the minimum population size of the Darwin’s Fox. Foxes were assumed to occupy 32% of the areas defined in the geographic range (see above). This number derives from the study in Nahuelbuta mentioned above (Moreira-Arce et al. 2015a), and is considered conservative especially when applied to Chiloé for three reasons. First, occupancy was not modelled at the home-range scale, but rather based on camera trap points; it is expected that increasing grain to the home range scale will also increase occupancy estimates. Second, Nahuelbuta is the northern limit of the distribution and the condition of the habitat is less favourable than in other areas such as Chiloé (J. Jiménez and D. Moreira pers. obs.), thus lower densities are expected in Nahuelbuta. Third, Nahuelbuta is located in an area that has been severely affected by land conversion (see Miranda et al. 2015), likely representing the most disturbed area within the current distribution of this fox. We then assumed that in occupied areas the density of mature foxes was 0.2 foxes/km². This number was calculated (1/488) from the largest home range (488 ha) reported in Jiménez (2007) and assumes that mature foxes do not have overlapping home ranges, an assumption that is extremely conservative as Jiménez (2007) showed high home range overlap (and a density of 0.92 foxes/km²). This procedure was equivalent to applying a density of 6.6 foxes/100 km². We did not attempt to estimate an upper limit of the population size. As a result we estimated a minimum of 412 mature individuals for Chiloé and 227 mature individuals for the areas in mainland where the fox is known to be present. If considering the areas where the fox is potentially extant, the minimum population size in mainland would approach 489 individuals.

Menaces identifiées(4 menaces classées CMP-IUCN)

  • 2_2_2
    Agro-industry plantations
    Negligible declinesMajority (50-90%)Ongoing
  • 8_1_2
    Named species
    Slow, Significant DeclinesMajority (50-90%)Ongoing
  • 5_1_3
    Persecution/control
    No declineMinority (<50%)Ongoing
  • 8_5_2
    Named species
    Very Rapid DeclinesMinority (<50%)Ongoing
Description complète des menacesExpert

Domestic dogs and associated diseases are likely the main threats for Darwin’s Foxes (Jiménez and McMahon 2004). Dogs are a common problem in Chilean protected areas, including each of those where the Darwin’s Fox is present. Domestic dogs would represent a risk for foxes through intra-guild killing, as well as through disease transmission (Jiménez and McMahon 2004, Cabello et al. 2013a,b). The death of Darwin’s Foxes due to dog attacks has been reported both on the mainland (D’Elia et al. 2013) and in Chiloé (Espinosa 2011, J. Jiménez pers. obs.). Moreira-Arce et al. (2015a) found a negative correlation between the areas used by dogs and foxes in Nahuelbuta. Accordingly, in Chiloé Island, Darwin’s Foxes are rare or absent from old-growth forests frequently visited by dogs, while they are frequently recorded at camera traps in scrublands when dogs are absent (A. Farías pers. obs.), suggesting spatial displacement. It is important to note that the dog problem that affects Darwin’s Foxes, is caused in most, if not all, cases by poorly managed free-ranging dogs and not feral dogs (D. Moreira pers. obs., E.A. Silva-Rodríguez et al. pers. obs.).

The risk of disease spillover from dogs (mainly Canine Distemper Virus, CDV) is considered a major threat for Darwin’s Fox populations (e.g., Jiménez and McMahon 2004, Silva-Rodríguez et al. 2015). Exposure of dogs to CDV has been shown in the proximity of Nahuelbuta National Park (Acosta-Jamett et al. 2015b) and Valdivian Coastal Reserve-Alerce Costero National Park (Sepúlveda et al. 2014). Furthermore, exposure to CDV has been reported for invasive American minks (Neovison vison) in areas were the Darwin’s Fox is present (Sepúlveda et al. 2014), as well as for Chilla (Lycalopex griseus) and Culpeo (Lycalopex culpaeus) in other regions (Acosta-Jamett et al. 2015a). Additionally, Jiménez et al. (2012) reported the death of three radio-collared foxes in Chiloé in sympatry with free-ranging dogs, suggesting that mortality could have been caused by CDV, although conclusive evidence was not available. CDV epizootics in canids have been reported worldwide (e.g., Goller et al. 2010, Di Sabatino et al. 2014), and CDV was implicated in a major decline in the population of the Island Fox (Urocyon littoralis) in Santa Catalina Island (Timm et al. 2009). In South America, Megid et al. (2009, 2010) reported CDV-related mortalities in wild canids in Brazil, and in Chile, Moreira and Stutzin (2005) reported the death of 27 Chilla and Culpeo foxes due to CDV in Coquimbo Region. The lack of conclusive evidence of declines due to CDV in the Darwin’s Fox may be well explained by lack of information, rather than by the absence of outbreaks.

Darwin’s Foxes can also be subject to human-caused mortality. According to J. Jiménez (pers. obs.) and Espinosa (2011), local people in Chiloé reported killing foxes because they attack domestic animals and to obtain their fur. Foxes rescued from traps as well as captured and translocated after predation on poultry have also been reported in Chiloé (J. Cabello pers. obs.). Stowhas (2012) also indicated that local people reported killing foxes (undetermined species) in an area that included the surroundings of Oncol Park, Alerce Costero National Park, and Valdivian Coastal Reserve, as a response to predation on poultry. In Nahuelbuta range, foxes (without distinguishing to the level of species) are often considered as problem animals (Sánchez et al. 2014). However, Darwin’s Fox is not commonly persecuted or killed by local people (but see McMahon et al. 1999) and its conservation would show a high social support (D. Moreira pers. obs.).

Forest loss is an important threat. The highest rates of forest loss occur in the coastal range of the Araucanía Region, where Nahuelbuta is located. There, the annual loss rate observed for the 1999-2008 period reached 4.8%, the second highest reported for Chilean temperate forest (Miranda et al. 2015). For the Valdivian Coastal Range, the net forest loss between 1985 and 2011 was 5.1% (and the gross loss reached 30%), but the loss rate was higher for the 1985-1999 period than for the 1999-2011 period (Zamorano-Elgueta et al. 2015). In northern Chiloé and Maullín, the annual rates of forest loss was close to 1% (1985-2007), although in the case of Chiloé this rate rose to 1.4% for the 1999-2007 period (Echeverría et al. 2012). Both in the Araucanía and Valdivian cases, cleared native forest was frequently converted to forestry plantations (Miranda et al. 2015, Zamorano-Elgueta et al. 2015). Although Darwin’s Fox has been recorded in plantations (Farías et al. 2014, J. Jiménez pers. obs.), evidence from the population in Nahuelbuta shows that foxes select for native forest (Moreira-Arce et al. 2015a). However, if managed through an increase of native understory cover, commercial plantations may provide complementary habitats and food resources for this species (Moreira-Arce et al. 2015b). Human-induced fires are an always-latent threat, especially for the Nahuelbuta range (D. Moreira pers. obs.). On the other hand, deforestation may favour other (larger sized) fox species (i.e. Lycalopex griseus and L. culpaeus), better adapted to open areas (e.g., Silva-Rodríguez et al. 2010), which can displace Darwin’s Foxes (Jiménez et al. 1991). The indirect effects of changes in land cover through alteration of interaction webs are still insufficiently known.

Indirect threats that need to be considered include the construction of bridges, highways and roads. Of major concern is the projected construction of the bridge connecting Chiloé to the mainland. This bridge, if barriers are not implemented, may facilitate the invasion of the island by other species such as congeneric foxes and Pumas (Puma concolor), with unknown, but potentially serious consequences for these populations. Road construction and improvement is an additional concern, given that they facilitate dog (Moreira-Arce et al. 2015a, Sepúlveda et al. 2015) and human movement, and can lead to land cover change (Wilson et al. 2005). Existing roads, as well as the construction of new roads and/or the improvement of existing public roads, is a concern for Nahuelbuta (Sánchez et al. 2014), the Valdivian Coastal Range (Silva-Rodríguez et al. 2015) and for Chiloé (J. Cabello pers. obs.).

Other threats that need to be taken into account include the translocation of rescued and problem animals (J. Cabello pers. obs.) and illegal tenure of foxes as pets (J. Jiménez pers. obs.).

Habitats préférentiels (classification IUCN)

  • 1_4Forest - Temperate
  • 3_4Shrubland - Temperate
  • 14_2Artificial/Terrestrial - Pastureland
  • 14_3Artificial/Terrestrial - Plantations
Mesures de conservation recommandéesExpert

Legislation
Included on CITES - Appendix II. Protected by Chilean law since 1929 (Iriarte and Jaksic 1986). Darwin’s Fox is listed as endangered in Chile (DS 151/2007 MINSEGPRES). Since 2012, the Ministry of the Environment is working in the elaboration of the Recovery, Conservation and Management plan for the species (RECOGE for its Spanish acronym), but this plan is not in effect yet.

Presence in protected areas
The Darwin’s Fox occurs in the following public protected areas: Nahuelbuta National Park (Araucanía Administrative Region), Alerce Costero National Park (Los Ríos Administrative Region), and Chiloé National Park (Los Lagos Administrative Region). In addition, the species is found in the following private protected areas: Caramávida Reserve (Biobío Administrative Region), Oncol Park and Valdivian Coastal Reserve (Los Ríos Administrative Region), and Tantauco, Ahuenco and Tepuhueico Parks (Los Lagos Administrative Region). Some of these protected areas are targeting the species through monitoring, supporting research or attempting to address the dog problem (e.g., Sánchez et al. 2014, Silva-Rodríguez et al. 2015). The Darwin’s Fox is one of the conservation targets (Darwin’s Fox, guigna and pudu) of the Valdivian Coastal Reserve (Silva-Rodríguez et al. 2015). Following the criteria by Simonetti and Mella (1997), and the densities reported by Jiménez (2007), it is possible to assume that good quality areas of around 550 km² in size could sustain ~500 individuals (Silva-Rodríguez et al. 2015). Tantauco Park in Chiloé, and the area protected by the Valdivian Coastal Reserve and Alerce Costero National Park as a whole, are the only protected areas that meet this criterion, although this does not guarantee the existence of such a number of foxes, as they appear to be scarcer in the Valdivian population (E. A. Silva-Rodríguez and A. Farías, pers. obs.), and the density of foxes in Ahuenco could be much higher than in other areas (Jiménez 2007).

Species-based measures
Vaccination of dogs against CDV has been conducted around some of the above-mentioned protected areas with the aim of preventing disease outbreaks that could affect Darwin’s Foxes (e.g., Sánchez et al. 2014, Silva-Rodríguez et al. pers. obs.). Current efforts to understand problems related to disease and its management in this species include the project ”Saving Darwin’s Fox: A Conservation Medicine Approach” led by Buin Zoo and several local organizations including among them Chiloé Silvestre and Parque Tantauco, as well as several universities.

Environmental education efforts are being conducted by several stakeholders. These include efforts by the Ministry of Environment, CONAF (Chile’s Forest Service), as well as private organizations such as the Committee for the Rescue of Nahuelbuta, Tantauco and The Nature Conservancy.

Presence in captivity
Currently, the only known captive Darwin’s Foxes are kept by Fauna Andina near Villarrica, where successful reproduction has been achieved in two consecutive years. These animals have been rescued from dog attacks and illegal ownership from Chiloé (F. Vidal pers. comm.).

Gaps in knowledge
Most known populations are currently being studied by researchers from multiple institutions. Key topics under study include genetics (J. Cabello pers. obs.), disease (E. Hidalgo pers. comm.), occupancy and habitat use (Silva-Rodríguez et al. pers. obs.). The later topic still deserves clarification regarding (1) the presence of the species between the Bueno and Maullín rivers (i.e. coastal mountain range of Osorno Province), (2) its potential presence in the Andes and lowlands between the Andes and the Coastal Range, and (3) under-explored areas in continental Chiloé. Furthermore, accurate information is needed regarding the abundance of the species in each of these populations.

Key issues that need to be addressed include the management of domestic dogs. Irresponsible ownership is the rule rather than the exception in Chile. Despite long legislative discussion, no serious solution is in place for this problem. Effective enforcement of responsible ownership is absolutely necessary to address this problem. Recently CONAF passed some rules that limit the entrance of dogs to protected areas (CONAF 2015), but these measures need to be supported by a coherent legislation.

The adequate management of exotic plantations is an important priority. Recent studies suggest that several forest species can use forest plantations if they have dense native understory (Simonetti et al. 2013). Thus, leaving understory in exotic tree plantations may be key to maintain connectivity in Darwin’s Fox populations, especially in Nahuelbuta (Moreira-Arce et al. 2016). The challenge is to implement these recommendations.

Actions de conservation (3)Expert
  • 1_1Site/area protection
  • 2_1Site/area management
  • 5_4_2National level
Stress écologiques (6)Expert
  • 1_1Ecosystem conversion
  • 1_2Ecosystem degradation
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_2Species disturbance
Usage & commerce (2)Expert
  • 10Wearing apparel, accessories
    subsistance
  • 13Pets/display animals, horticulture
    subsistance
Priorités de recherche (2)Expert
  • 1_2Population size, distribution & trends
  • 1_5Threats
Niche IUCN globaleExpert

Royaumes biogéographiques

Neotropical

Systèmes (terrestre/eau douce/marin)

Terrestrial
Références bibliographiques (30)Expert
  1. IUCN. 2016. The IUCN Red List of Threatened Species. Version 2016-3. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 07 December 2016).
  2. 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).
  3. Moreira-Arce, D., Vergara, P.M., Boutin, S., Carrasco G., Briones, R., Soto, G.E. and Jiménez. J.E. 2016. Mesocarnivores respond to fine-grain habitat structure in a mosaic landscape comprised by commercial forest plantations in Southern Chile. <i>Forest Ecology and Management</i> 369: 135-143.
  4. Moreira-Arce, D., Vergara, P.M., Boutin, S., Simonetti, J.A., Briceño, C. and Acosta-Jamett, G. 2015b. Native forest replacement by exotic plantations triggers changes in prey selection of mesocarnivores. <i>Biological Conservation</i> 192: 258-267.
  5. Acosta-Jamett, G., Surot, D., Cortés, M., Marambio, V., Valenzuela, C., Vallverdu, A. and Ward, M. P. 2015b. Epidemiology of canine distemper and canine parvovirus in domestic dogs in urban and rural areas of the Araucanía region in Chile. <i>Veterinary Microbiology</i> 178: 260-264.
  6. Moreira-Arce, D., Vergara, P.M. and Boutin S. 2015a. Diurnal human activity and introduced species affect occurrence of carnivores in a human-dominated landscape. <i>PLoS ONE</i> 10(9): e0137854.
  7. Acosta-Jamett, G., Cunningham, A.A. and Cleaveland, S. 2015a. Serosurvey of canine distemper virus and canine parvovirus in wild canids and domestic dogs at the rural interface in the Coquimbo Region, Chile. <i>European Journal of Wildlife Research </i> 61: 329-332.
  8. Sepúlveda, M., Pelican, K., Cross, P., Eguren, A. and Singer, R. 2015. Fine-scale movements of rural free-ranging dogs in conservation areas in the temperate rainforest of the coastal range of southern Chile. . <i>Mammalian Biology </i> 80: 290-297.
  9. Silva-Rodríguez, E.A., Sepúlveda, M.A., Duarte, C., Stowhas, P., García-Vera, C., Cruz. E., Travieso, G., Zorondo-Rodríguez, F., Alfonso, A., Godoy, M., Andrade, A., Osman, L., Pezoa, L., Zamorano, S., Poveda, P. and Almonacid, A. 2015. Plan de Conservación de Área, Reserva Costera Valdiviana. The Nature Conservancy, Valdivia, Chile.
  10. Miranda, A., Altamirano, A., Cayuela, L., Pincheira, F. and Lara, A. 2015. Different times, same story: Native forest loss and landscape homogenization in three physiographical areas of south-central of Chile. <i>Applied Geography</i> 60: 20-28.
  11. CONAF. 2015. Normativa para el manejo de perros y otras mascotas en las areas silvestres protegidas administradas por CONAF. Corporación Nacional Forestal (CONAF), Ministerio de Agricultura, Chile. Santiago.
  12. Zamorano-Elgueta, C., Benayas, J.M.R., Cayuela, L., Hantson, S. and Armenteras, D. 2015. Native forest replacement by exotic plantations in southern Chile (1985–2011) and partial compensation by natural regeneration. <i>Forest Ecology and Management</i> 345: 10-20.
  13. Farías, A.A., Sepúlveda, M.A., Silva-Rodríguez, E.A., Eguren, A., González, D., Jordán, N. I., Ovando, E., Stowhas, P. and Svensson, G.L. 2014. A new population of Darwin’s Fox (<i>Lycalopex fulvipes</i>) in the Valdivian Coastal Range. <i>Revista Chilena de Historia Natural</i> 87: 1-3.
  14. Sánchez, P., Guiñez, P., Cárcamo, J. and Rojas, C. 2014. Conservación de zorro de Darwin (<i>Lycalopex fulvipes</i>) implementando medidas de mitigación a sus principales amenazas en el Parque Nacional Nahuelbuta, Región de La Araucanía. <i>Biodiversidata </i> 2: 83-88.
  15. Di Sabatino, D., Lorusso, A., Di Francesco, C.E., Gentile, L., Di Pirro, V., Bellacicco, A.L., Giovannini, A., Di Francesco, G., Marruchella, D., Marsilio, F. and Savini, G. 2014. Arctic Lineage-Canine Distemper Virus as a Cause of Death in Apennine Wolves (<italic>Canis lupus</italic>) in Italy. <i>PLOS One</i> 9(1): e82356.
  16. Cabello, J.E. and Dávila, J.A. 2014. Isolation and characterization of microsatellite loci in Darwin’s fox (<i>Lycalopex fulvipes</i>) and cross-amplification in other canid species. <i>Conservation Genetics Resources</i> 6: 759-761.
  17. Sepúlveda, M.A., Singer, R.S., Silva-Rodríguez, E., Eguren, A., Stowhas, P. and Pelican, K. 2014. Invasive American mink: linking pathogen risk between domestic and endangered carnivores. <i>EcoHealth</i> 11: 409-419.
  18. Cabello, J.E., Altet, L., Napolitano, C., Sastre, N., Hidalgo, E., Dávila, J.A. and Millán, J. 2013b. Survey of infectious agents in the endangered Darwin's fox (<i>Lycalopex fulvipes</i>): High prevalence and diversity of hemotrophic mycoplasmas. <i>Veterinary Microbiology</i> 167: 448-454.
  19. Cabello, J.E., Esperón, F., Napolitano, C., Hidalgo, E., Dávila, J.A. and Millan, J. 2013a. Molecular identification of a novel gammaherpesvirus in the endangered Darwin’s fox (<i>Lycalopex fulvipes</i>). <i>Journal of General Virology</i> 94: 2745-2749.
  20. Simonetti, J.A., Grez, A.A. and Estades C.F. 2013. Providing habitat for native mammals through understory enhancement in forestry plantations. <i>Conservation Biology</i> 27: 1117-1121.
  21. Austin, J.J., Soubrier, J., Prevosti, F.J., Prates, L., Trejo, V., Mena, F. and Cooper, A. 2013. The origins of the enigmatic Falkland Islands wolf. <i>Nature Communications</i> 4: 1552.
  22. D'Elía, G., Ortloff, A., Sánchez, P., Guíñez, B. and Varas, V. 2013. A new geographic record of the endangered Darwin’s Fox <i>Lycalopex fulvipes</i> (Carnivora: Canidae): filling the distributional gap . <i>Revista Chilena de Historia Natural</i> 86: 485-488.
  23. Stowhas, P. 2012. Conflicto Entre Carnívoros Silvestres y Campesinos en el sur de Chile. DVM thesis. Universidad Mayor, Santiago, Chile.
  24. Echeverría, C., Newton, A., Nahuelhual, L., Coomes, D. and Rey-Benayas, J. M. 2012. How landscapes change: Integration of spatial patterns and human processes in temperate landscapes of southern Chile. <i>Applied Geography</i> 32: 822-831.
  25. Jiménez, J.E., Briceño, C., Alcaíno, H., Vásquez, P., Funk, S. and González-Acuña, D. 2012. Coprologic survey of endoparasites from Darwin’s Fox (<i>Pseudalopex fulvipes</i>) in Chiloé, Chile. <i>Archivos de Medicina Veterinaria</i> 44: 93-97.
  26. Espinosa, M.I. 2011. Dieta y uso de hábitat del huillín (<i>Lontra provocax</i>) en ambientes de agua dulce y su relación con comunidades locales en el bosque templado lluvioso, Isla Grande de Chiloé, Chile . DVM thesis, Universidad Mayor, Santiago .
  27. Farías, A.A. and Jaksic, F.M. 2011. Low functional richness and redundancy of a predator assemblage in native forest fragments of Chiloé Island, Chile. <i>Journal of Animal Ecology</i> 80: 809-817.
  28. Perini, F.A., Russo, C.A.M. and Schrago, C.G. 2010. The evolution of South American endemic canids: a history of rapid diversification and morphological parallelism. <i>Journal of Evolutionary Biology</i> 23: 311-322.
  29. Goller, K.V., Fyumagwa, R.D., Nikolin, V., East, M.L., Kilewo, M., Speck, S., Müller, T., Matzke, M. and Wibbelt, G. 2010. Fatal canine distemper infection in a pack of African wild dogs in the Serengeti ecosystem, Tanzania. <i>Veterinary Microbiology </i> 146: 245–252.
  30. Megid, J., Teixeira, C.R., Amorin, R.L., Cortez, A., Heinemann, M.B., de Paula Antunes, J.M., da Costa, L.F., Fornazari, F., Cipriano, J.R., Cremasco, A. and Richtzenhain, L.J. 2010. First identification of canine distemper virus in hoary fox (<i>Lycalopex vetulus</i>): pathologic aspects and virus phylogeny. <i>Journal of Wildlife Diseases</i> 46: 303-305.
Évaluateurs & contributeurs (3)Expert
assessor
Silva-Rodríguez, E, Farias, A., Moreira-Arce, D., Cabello, J., Hidalgo-Hermoso, E., Lucherini, M. & Jiménez, J.
evaluator
Hoffmann, M. & Sillero-Zubiri, C.
facilitators
Hoffmann, M. & Thresher, S.
1 erratum publié après l'évaluation.

Silva-Rodríguez, E, Farias, A., Moreira-Arce, D., Cabello, J., Hidalgo-Hermoso, E., Lucherini, M. & Jiménez, J. 2016. Lycalopex fulvipes (errata version published in 2016). The IUCN Red List of Threatened Species 2016: e.T41586A107263066. Accessed on 05 May 2026.

Traits biologiques

20 valeurs · 4 sources

Morphologie(4)

Masse adulte
-999000 mg
PanTHERIA
Longueur
-999 mm
PanTHERIA
Masse naissance
-999000 mg
PanTHERIA
Masse au sevrage
-999000 mg
PanTHERIA

Cycle de vie(1)

Longévité max
-999 mois
PanTHERIA
Voir 15 traits de plus (2 catégories)

Reproduction(6)

Gestation
-999 j
PanTHERIA
Intervalle naissances
-999 j
PanTHERIA
Taille de portée
-999
PanTHERIA
Portées par an
-999
PanTHERIA
Maturité sexuelle
-999 j
PanTHERIA
Sevrage
-999 j
PanTHERIA

Écologie & habitat(9)

Fruits (%)
20 %
elton_mammals
Invertébrés (%)
20 %
elton_mammals
Nectar (%)
0 %
elton_mammals
Autre végétal (%)
0 %
elton_mammals
Charognard (%)
0 %
elton_mammals
Graines (%)
0 %
elton_mammals
Vert. ectothermes (%)
20 %
elton_mammals
Vert. endothermes (%)
40 %
elton_mammals
Poissons (%)
0 %
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 (heatmap GBIF)Construction en cours

0 obs · 0 cellules
Construction par partitions temporelles GBIF0%

Source : GBIF — observations agrégées par hexagones 0.2° × 0.2° (~22km). Filtre qualité : précision coordonnée < 10 km. Coloration quantile (q50/70/90/99). Fond carte : OpenFreeMap · © OpenStreetMap.

Distribution mondiale

Calcul de la distribution GBIF· ~10–60 s

Phénologie

Calcul du calendrier d'apparition· ~5–30 s

Consulter sur les bases externes

Observations & statuts

Cartographie

Bibliographie

Note nomenclaturale & synonymesExpert

Note nomenclaturale

TAXREF v18 — INPN/MNHN

Synonymes (2)— redirigent vers cette page

  • Pseudalopex fulvipes(Martin, 1837)
  • Vulpes fulvipesMartin, 1837

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