
Ours Andin
Tremarctos ornatus(F. 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 Tremarctos ornatus 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
82 partenaires écologiques documentés directement dans GloBI.
Liste rouge IUCN
VU · Vulnérablecritères A3c+4c↘Décroissante- Évaluation
- 2017 · v3.1
- Altitude
- 200 – 4750 m
- Profondeur
- – m
État de la populationTexte officiel évaluation IUCNExpert
Expert knowledge, data extrapolations, genetic analysis, mark-recapture, radio tracking and sign surveys, as well as ecological modelling have been used to estimate population sizes and densities of Andean Bears (Peyton 1984, 1999; Yerena 1994; Peyton et al. 1998; Cuesta and Suárez 2001; Ruiz-García 2003; Kattan et al. 2004; Viteri 2007; Ríos-Uzeda et al. 2007; Velez-Liendo 2010; Garshelis 2011; García-Rangel 2012). Wild populations are believed to be on decline due to habitat loss and fragmentation, and illegal killing (Rodríguez et al. 2003, Kattan et al. 2004, Yerena et al. 2007, Sánchez-Mercado et al. 2008, Velez-Liendo et al. 2009, Velez-Liendo and Paisley 2010, García-Rangel 2012). National assessments applying different approaches estimated 1,100-1,600 bears in Venezuela (Ruiz-García 2003), 3,000-6,000 in Colombia (Ruiz-García 2003), 1,200-2,000 in Ecuador (Cuesta and Suárez 2001, Viteri 2007), ~5,000 bears in Peru (Peyton 1999), and ~3,000 bears in Bolivia (Velez-Liendo 2010). These rather crude countrywide estimates, yielding a range-wide estimate of 13,000-18,000 bears (5-7 bears/100 km² over its 260,000 km² range), are reasonably consistent with three empirically-derived mark-recapture (re-sight) density estimates of 3-8 bears/100 km² (Viteri 2007, Ríos-Uzeda et al. 2007, S. Molina, pers. comm). It should be cautioned, however, that all abundance and density estimates for this species have known biases, so consistency among the estimates is not verification of their accuracy (Garshelis 2011).
Menaces identifiées(14 menaces classées CMP-IUCN)
4_1Roads & railroadsRapid DeclinesMajority (50-90%)Ongoing11_2DroughtsSlow, Significant DeclinesMajority (50-90%)Ongoing11_3Temperature extremesSlow, Significant DeclinesMajority (50-90%)Ongoing11_4Storms & floodingSlow, Significant DeclinesMajority (50-90%)Ongoing2_1_1Shifting agricultureSlow, Significant DeclinesMajority (50-90%)Ongoing2_1_2Small-holder farmingSlow, Significant DeclinesMajority (50-90%)Ongoing2_1_3Agro-industry farmingSlow, Significant DeclinesMinority (<50%)Ongoing2_3_1Nomadic grazingSlow, Significant DeclinesMinority (<50%)Ongoing2_3_2Small-holder grazing, ranching or farmingSlow, Significant DeclinesMajority (50-90%)Ongoing3_1Oil & gas drillingSlow, Significant DeclinesMajority (50-90%)Ongoing
+ 4 menaces supplémentaires
Description complète des menacesTexte détaillé évaluation IUCNExpert
Habitat Loss
The Tropical Andes has been home to human communities, including the great Inca Empire, for thousands of years and, as a consequence, 90% of Andean ecosystems have been transformed in some way (Young 1998, 2009; Vina and Cavelier 1999; Ataroff and Rada 2000; Myers et al. 2000; Kattan et al. 2004; Armenteras et al. 2011). The expansion of the agricultural frontier, together with inadequate agricultural practices and land/agrarian reforms, have been the main drivers of the loss of natural ecosystems (Peyton et al. 1998, Yerena 1998, Young 1998, Vina and Cavelier 1999, Ataroff and Rada 2000, Armenteras et al. 2011, Portillo-Quintero et al. 2012). Mining and oil exploitation are becoming an increasing menace not only to bears, but to local communities due to land expropriation, loss of habitat connectivity, and contamination of water and soil (Young and León 1999, Bury 2002, Bebbington et al. 2008, Bebbington 2009). Conversion of land to coca crops and the drug trade, together with guerrilla groups in some parts of the Andes, favours a lawless land-use system that also impacts the quality of Andean Bear habitats and the bear's probability of long-term survival (Rodríguez et al. 2003, Yerena et al. 2007, Dávalos et al. 2011, García-Rangel 2012).
Illegal Killing
Illegal killing is an important, but underestimated threat for Andean Bears. Based on a review of the literature, an average of about 180 bears are known to be killed per year across its range—it is suspected that the real number is much higher, and is likely increasing. For example, recent assessments in northern Ecuador showed unprecedented numbers of cattle killed by bears (at least 320 during the period 2009-2014; Zukowski and Ormsby 2016), as more people are turning to dairy cow farming as a livelihood (Jampel 2016). Bears are killed for retaliation against crop or livestock depredations (or protection against future depredations), for cultural or medical beliefs, and for commercial trade (Orejuela and Jorgenson 1999, Peyton 1999, Rumiz and Salazar 1999, Rodríguez et al. 2003, Yerena et al. 2007, Figueroa 2008, Figueroa and Stucchi 2009, Lameda 2011, E.D. Rodríguez pers. comm. 2014, M.P. Viteri pers. comm. 2014). Since the number of bears killed is likely underestimated by a wide margin, the effects of such killing on bear populations is hard to assess, but rates of killing are high in some areas. Sanchez-Mercado et al. (2008, 2014) estimated that up to 36% of the bear’s distribution in the Cordillera de Merida in Venezuela was within an “ecological trap”, due to human threats. These authors estimated that the effects of this threat combined with habitat fragmentation could be fostering an extinction probability higher than 50% over the next 50 years across this mountain range. Bears are killed during opportunistic encounters, while sport hunting, or as retaliation after damaging crops, particularly maize, or killing livestock (Goldstein 1991, 2002; Peyton 1999, Poveda 1999, Morales Vargas 2003, Goldstein et al. 2006, Sánchez-Mercado et al. 2008, Torres 2008).
Climate Change
Global projections of effects of climate change show a general tendency towards upslope displacement of the mountain biome, suggesting that the Tropical Andes is among the most vulnerable region to climate change (Malcom et al. 2006, Urrutia and Vuille 2009, Beaumont et al. 2011). However, the heterogeneity of this hotspot shows a more complex response (Tovar et al. 2013) affecting phenological patterns and increasing species vulnerability with predictions of species loss ranging from 20-50% due to range contractions for many taxa (Cuesta-Camacho et al. 2008, Lawler et al. 2009, Aguirre et al. 2011, Graham et al. 2011, Hoffmann and Sgrò 2011, Chen et al. 2011, Velásquez-Tibatá et al. 2013, Richardson et al. 2013, Pacifici et al. 2015).
It is likely that all ecosystems associated with Andean Bears will exhibit reductions in their extension. With an increment of +0.74 C in the last century, and a projected increase of 4.3 +/- 0.7 C by 2100 (IPCC 2013), extensive changes in habitat are expected: the Tropical high altitude grasslands is the most fragile ecosystem, with an estimated loss of 30% (Tovar et al. 2013) due to the lack of upslope area for migration. Projected reduction in annual rainfall (IPCC 2013) is likely to affect species highly dependent on humidity such as epiphytic bromeliads (Colwell et al. 2008, Svenning and Condit, 2008, Tewsksbury et al. 2008). Tropical dry and moist shrublands are likely to lose 24% of their area (Tovar et al. 2013), mainly due to a significant variation in the number of dry months (IPCC 2013), while a loss of 18% in area was estimated for Tropical moist lowland and montane forests and Tropical dry forests due to upslope displacements. Furthermore, the extensive (and intensive) land use by human activities in Paramo grasslands, are likely to encroach even further, affecting not only the biodiversity associated to this ecosystem, but also the ecosystem services this biome provides to the region.
Changes in climate regimes must therefore be considered as a growing threat for Andean Bears, as they are likely to alter habitat quality as well as land-use patterns, and increase the probability of human–bear encounters and conflict (Karanth and Chellam 2009, Aguirre et al. 2011, Hoffmann and Sgrò 2011, Chen et al. 2011, Sheridan and Bickford 2011, Mysterud 2013, Ripple et al. 2014). Even more, the areas considered to be most vulnerable to climate change across the Andes are those considered important for Andean bears including: Yanachaga Chemillen National Park (NP) (Peru), Manu NP (Peru), Madidi NP (Bolivia), Apolobamba ANMI (Bolivia), Carrasco NP (Bolivia) and Amboro NP (Bolivia) (Hoffman et al. 2011).
Habitats préférentiels (classification IUCN)
1_5Forest - Subtropical/Tropical Dry★1_6Forest - Subtropical/Tropical Moist Lowland★1_9Forest - Subtropical/Tropical Moist Montane★3_5Shrubland - Subtropical/Tropical Dry★3_6Shrubland - Subtropical/Tropical Moist★3_7Shrubland - Subtropical/Tropical High Altitude★4_7Grassland - Subtropical/Tropical High Altitude★
Mesures de conservation recommandéesStratégies de conservation IUCNExpert
The Andean Bear has been listed as Vulnerable by the IUCN since 1982 and has been included in CITES Appendix I since 1975. A total of 58 protected areas have been established across the Andean Bear distribution, but threats remain within their boundaries with most of these areas being no more than “Paper Parks” lacking adequate budget and staff (Hardner 2008; Sánchez-Mercado et al. 2008; Monsalve Dam et al. 2010; García-Rangel 2011, 2012). Although efforts to establish, maintain and connect old and new protected areas along the bear’s range have been carried out (e.g., Vilcabamba-Amboro corridor between Peru and Bolivia and the interconnected system of protected areas in the Venezuela Andes), large portions of the bear’s habitat are still unprotected and poaching has not been controlled (Yerena 1994, 1998;Yerena et al. 2003, Kattan et al. 2004, Surkin et al. 2010, Yerena and García-Rangel 2010, Hoffman et al. 2011, Sánchez-Mercado et al. 2014). Recently (2007-2014), a number of important steps towards Andean Bear conservation have been undertaken across its distribution including: (1) promotion of Andean Bear conservation by local education programmes and research projects carried out by conservation groups, NGOs, zoological parks, universities, research institutes and government agencies in Bolivia, Peru and Venezuela (Figueroa and Stucchi 2009, Albarracín 2010, García-Rangel 2012). (2) The publication of national action plans for Venezuela, Colombia and Ecuador (Sánchez-Mercado 2008, Castellanos et al. 2010, Monsalve Dam et al. 2010), and a national assessment for Bolivia (Velez-Liendo, et al. 2009). Unfortunately priority actions highlighted by some of these programs have not been undertaken. Such is the case for the three key areas identified for connectivity conservation within the Venezuelan Action Plan (Yerena et al. 2007).
Knowledge regarding the species ecology has improved, with information about home range sizes, movement patterns and population sizes for some locations in Peru, Ecuador and Colombia (Rodríguez et al. 2003, Monsalve Dam et al. 2010, Sánchez-Mercado et al. 2010, García-Rangel 2012). Nevertheless, in order to develop robust conservation actions, further efforts regarding population sizes and limiting factors are required. Current and future research need to focus on populations, habitat and connectivity, human dimensions, and climate change effects on both the ecology of the species and human-bear conflict (Rodríguez et al. 2003, Jorgenson and Sandoval 2005, Yerena et al. 2007, Monsalve Dam et al. 2010, Velez-Liendo and Paisley 2010, García-Rangel 2012). Finally, it is important to encourage conservation initiatives to focus on a more holistic and creative approach where the needs of the species and the people inhabiting the Andes mountain range are jointly considered (García-Rangel 2012).
Actions de conservation (15)Conservation Actions Classification Scheme — IUCNExpert
1_1Site/area protection1_2Resource & habitat protection2_1Site/area management2_3Habitat & natural process restoration4_1Formal education4_2Training4_3Awareness & communications5_1_2National level5_1_3Sub-national level5_2Policies and regulations5_3Private sector standards & codes5_4_2National level6_1Linked enterprises & livelihood alternatives6_4Conservation payments6_5Non-monetary values
Stress écologiques (20)Stresses Classification — IUCNExpert
1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_1Ecosystem conversion1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_2Ecosystem degradation1_3Indirect ecosystem effects2_1Species mortality2_1Species mortality2_1Species mortality2_1Species mortality2_2Species disturbance2_2Species disturbance2_2Species disturbance
Usage & commerce (3)Use & Trade — IUCNExpert
1Food - humansubsistance13Pets/display animals, horticulturenational3Medicine - human & veterinarysubsistance
Priorités de recherche (8)Research Needed Classification — IUCNExpert
1_2Population size, distribution & trends1_5Threats1_6Actions2_1Species Action/Recovery Plan2_3Harvest & Trade Management Plan3_1Population trends3_3Trade trends3_4Habitat trends
Niche IUCN globaleRealms · Systems · LMEs · Growth forms · FAOs — biogéographie IUCNExpert
Royaumes biogéographiques
Systèmes (terrestre/eau douce/marin)
Références bibliographiques (30)Sources scientifiques de l'évaluation IUCNExpert
- IUCN. 2018. The IUCN Red List of Threatened Species. Version 2018-1. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 28 June 2018).
- IUCN. 2017. The IUCN Red List of Threatened Species. Version 2017-3. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 5 December 2017).
- Zukowski, B. and Ormsby, A. 2016. Andean bear livestock depredation and community perceptions in northern Ecuador. <i>Human Dimensions of Wildlife</i> 21: 111-126.
- Jampel, C. 2016. Cattle-based livelihoods, changes in the taskscape, and human–bear conflict in the Ecuadorian Andes. <i>Geoforum</i> 69: 84-93.
- Pacifici, M., Foden, W.B., Visconti, P., Watson, J.E.M., Butchart, S.H.M., Kovacs, K.M., Scheffers, B.R., Hole, D.G., Martin, T.G., Akçakaya, H.R., Corlett, R.T., Huntley, B., Bickford, D., Carr, J.A., Hoffmann, A.A., Midgley, G.F., Pearce-Kelly, P., Pearson, R.G., Williams, S.E., Willis, S.G., Young, B. and Rondinini, R. 2015. Assessing species vulnerability to climate change. <i>Nature Climate Change</i> 5(March 2015): 215-225.
- Sánchez-Mercado, A., Ferrer-Paris, J.R., García-Rangel, S., Yerena, E., Robertson, B.A., and Rodríguez-Clark, K.M. 2014. Combining threat and occurrence models to predict potential ecological traps for Andean bears in the Cordillera de Mérida, Venezuela. <i>Animal Conservation</i>.
- Velez–Liendo, X., Adriaensen, F. and Matthysen, E. 2014. Landscape assessment of habitat suitability and connectivity for Andean bears in the Bolivian Tropical Andes. <i>Ursus</i> 25(2): 172-187.
- Cosse, M., Del Moral Sachetti, J.F., Mannise, N. and Acosta, M. 2014. Genetic evidence confirms presence of Andean bears in Argentina. <i>Ursus</i> 25: 163-171.
- Ripple, W. J., J. A. Estes, R. L. Beschta, C. C. Wilmers, E. G. Ritchie, M. Hebblewhite, J. Berger, B. Elmhagen, M. Letnic, M. P. Nelson, O. J. Schmitz, D. W. Smith, A. D. Wallach, and A. J. Wirsing. 2014. Status and ecological effects of the world’s largest carnivores. <i>Science</i> 343(6167).
- Tovar C, Arnillas C.A., Cuesta F., and Buytaert, W. 2013. Diverging Responses of Tropical Andean Biomes under Future Climate Conditions. <i>PloS ONE</i> 8(5).
- Enciso, M.A. and Guimarães, M.A.B.V. 2013. Knowing the reproductive endocrinology in the female Andean bear through non-invasive methods. <i>International Bear News</i> 22: 33-34.
- Appleton, R., Tobler, M. and Van Horn, R. 2013. A Comparison of Andean Bear (<i>Tremarctos ornatus</i>) densities using camera traps at waterholes and bear trails in the tropical dry forest of Northwestern Peru. <i>International Association for Bear Research and Management, Provo, USA</i>: 38.
- Richardson, A. D., Keenan, T. F., Migliavacca, M., Ryu, Y., Sonnentag, O. and Toomey, M. 2013. Climate change, phenology, and phenological control of vegetation feedbacks to the climate system. <i>Agricultural and Forest Meteorology</i> 169: 156-173.
- Hansen, M.C., Potapov, P.V., Moore, R., Hancher, M., Turubanova, S.A., Tyukavina, A., Thau, D., Stehman, S.V., Goetz, S.J., Loveland, T.R., Kommareddy, A., Egorov, A., Chini, L., Justice, C.O. and Townshend, J.R.G. 2013. High-Resolution Global Maps of 21st-Century Forest Cover Change. Available at: <a href="http://www.earthenginepartners.appspot.com/science-2013-global-forest">http://www.earthenginepartners.appspot.com/science-2013-global-forest</a>. (Accessed: 2014).
- IPCC. 2013. Summary for Policymakers. <i>Climate Change 2013: The Physical Science Basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change</i>, Intergovernmental Panel on Climate Change. Cambridge University Press, New York.
- Mysterud, A. 2013. Ungulate migration, plant phenology, and large carnivores: The times they are a-changin’. <i>Ecology</i> 94: 1257-1261.
- Velásquez-Tibatá, J., Salaman, P. and Graham, C.H. 2012. Effects of climate change on species distribution, community structure, and conservation of birds in protected areas in Colombia. <i>Regional Environmental Change</i> 13(2): 235-248.
- García-Rangel, S. 2012. On Andean bear (<i>Tremarctos ornatus</i>) natural history and conservation. <i>Mammal Review</i> 42: 85-119.
- Portillo-Quintero, C., Larreal, J., Gonzalez, I., Sanchez, A. and Valbuena, C. 2012. Forest Cover and deforestation patterns in the northern Andes (Lake Maracaibo Basin): a synoptic assessment using MODIS and Landsat imagery. <i>Applied Geography</i> 35: 152-163.
- Castellanos, A. 2011b. Andean bear home ranges in the Intag region, Ecuador. <i>Ursus</i> 22: 65-73.
- Castellanos, A. 2011a. Do Andean Bears Attack Mountain Tapirs? <i>International Bear News</i> 20(4): 41-42.
- Hoffman, D., Oetting, I., Arnillas, C.A., and Ulloa, R. 2011. Cambio climático y áreas protegidas en los Andes Tropicales. In: S. K. Herzog, R. Martínez, P. M. Jørgensen, and H. Tiessen (eds), <i>Climate change and biodiversity in the Tropical Andes. Inter-American Institute for Global Change Research (IAI)</i>, pp. 426. Säo José dos Campos, and Scientific Committee on Problems of the Environment (SCOPE), Paris, France.
- Aguirre, L.F., Anderson, E.P., Brehm, G., Herzog, S.K., Jørgensen, P.M., Kattan, G.H., Maldonado, M., MartInez, R., Mena, J.L., Pabón, J.D., Seimon, A. and Toledo, C. 2011. Phenology and interspecific ecological interactions of Andean biota in the face of climate change. In: S.K. Herzog, R. Martínez, P.M. Jørgensen, and H. Tiessen (eds), <i>Climate change and biodiversity in the Tropical Andes. Inter-American Institute for Global Change Research (IAI)</i>, pp. 426. Säo José dos Campos, and Scientific Committee on Problems of the Environment (SCOPE), Paris, France.
- Sheridan, J.A., and Bickford, D. 2011. Shrinking body size as an ecological response to climate change. <i>Nature Climate Change</i> 1: 401–406.
- García-Rangel, S. 2011. Ecology and conservation of the Andean bear in Venezuela. University of Cambridge.
- Garshelis, D.L. 2011. Andean bear density and abundance estimates — How reliable and useful are they? <i>Ursus</i> 22: 47-64.
- Chen, I.-C., Hill, J.K., Ohlemüller, R., Roy, D.B. and Thomas, C.D. 2011. Rapid range shifts of species associated with high levels of climate warming. <i>Science</i> 333: 1024-1026.
- Lameda Camacaro, I. 2011. Etnozoología del oso andino (Tremarctos ornatus) en el noroeste de Argentina y la Cordillera Andina de Venezuela. Universidad Nacional de Salta, Salta, Argentina.
- FAO. 2011. State of the world's forests. Food and Agriculture Organization of the United Nations Rome.
- Beaumont, L.J., Pitman, A., Perkins, S., Zimmermann, N.E., Yoccoz, N.G. and Thuiller, W. 2011. Impacts of climate change on the world's most exceptional ecoregions. <i>Proceedings of the National Academy of Sciences</i> 108(6): 2306-2311.
Évaluateurs & contributeurs (3)Personnes ayant contribué à l'évaluation IUCNExpert
Velez-Liendo, X. & García-Rangel, S. 2017. Tremarctos ornatus (errata version published in 2018). The IUCN Red List of Threatened Species 2017: e.T22066A123792952. 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.
Chant
1 captation · Xeno-cantoHot-link CDN Xeno-canto. Chaque captation porte sa propre licence Creative Commons (visible quand la piste est active) et l'attribution de son auteur.
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
- Tremarctos lasalleiMaria, 1924
- Tremarctos ornatus majoriThomas, 1902
- Ursus frugilegusTschudi, 1844
- Ursus nasutusSclater, 1868
- Ursus ornatusF. G. Cuvier, 1825
- Ursus ornatus thomasiHornaday, 1911
Sources : Catalogue of Life Cross-References (synonymes) · TAXREF v18 INPN/MNHN (commentaires FR).