Ontologia
Otarie a fourrure

Otarie a fourrure

Callorhinus ursinus(Linnaeus, 1758)

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

40 partenaires écologiques documentés directement dans GloBI.

Partenaires
40
Espèces avec interactions documentées
Types d'interactions
7
Prédation, pollinisation, parasitisme…
Connectance
0.069
Densité des liens dans le sous-graphe affiché
Rang animalia
91 %
Percentile vs ensemble des animalia

Liste rouge IUCN

VU · Vulnérablecritères A2bDécroissante
Évaluation complète
Évaluation
2015 · v3.1
Altitude
10 m
Profondeur
207 m
État de la populationExpert
The population history for Northern Fur Seals throughout the North Pacific and Bering Seas has been tied to the harvest of seals for their pelts (Kuzin 1999, NMFS 2007). Between the mid 1700s and early 1800s, Russian sealers used Aleut labour to harvest an average of 100,000 Fur Seals, mostly pups, annually in Alaskan waters (Roppel 1984). The commercial harvest of Fur Seals on the Pribilof Islands continued with periodic modifications to the sex/age classes of focus until and after the United States purchase of Alaska in 1867. In the late 1800s and early 1900s commercial harvests on land and pelagic sealing continued unregulated until the Fur Seal act of 1911 was signed by Japan, Russia, Great Britain (for Canada) and the United States. This treaty prohibited pelagic sealing and reduced the take on land which at its peak in 1868 had harvested 240,000 seals in a single year (Roppel and Davey 1965, NMFS 2007).

In the early 1900s the Pribilof stock continued to grow in abundance despite commercial harvest. Between 40,000 and 126,000 seals were harvested each year during 1943-1968 (NMFS 2007). A new harvest regime was followed in the early 1960s which allowed for annual harvests of approximately 300,000 adult females and 30,000-96,000 subadult males (York and Hartley 1981). The population did not increase as anticipated after this new regime and ultimately commercial harvest of Fur Seals was terminated on St. George Island in 1973 and on St. Paul Island in 1983. Subsistence harvest of subadult males has continued on both islands since that time (NMFS 2007). In 2014, subsistence harvest rules were changed to allow the annual take of up to 150 male pups on St. George Island during a new autumn harvest season. This harvest occurred for the first time in the autumn of 2014.

Contrasting to the Northern Fur Seal abundance trend on the Pribilof Islands is Bogoslof Island, a small volcanic island in the eastern Aleutian Islands of Alaska. Northern Fur Seals were first reported on Bogoslof in 1976 with the first breeding seals noted in 1980 (Lloyd et al. 1981, Loughlin and Miller 1989). Subsequent surveys revealed an exponential growth rate during the 1990s and early 2000s with the estimated number of pups increasing at a rate of 48.5% annually between the time pups were first observed in 1980 and 2005. This rate then dropped to approximately 10% annually between 2005-2011, the last time the island was surveyed. Such a dramatic growth rate can only be explained by a combination of recruitment and immigration from other sites (Ream et al. 1999). Recent studies suggest that the recent slowing in growth rate coupled with increases in foraging trip duration and distance may represent a typical density dependent response to a limited resource (Kuhn et al. 2014). The Northern Fur Seal population on Bogoslof has increased to the point that it is the second largest Northern Fur Seal rookery in the United States, surpassing St. George Island. This growth has served to ameliorate the overall decline of the population.

Northern Fur Seal rookeries in Russia have not been counted since 2006-2009 depending on the site. However, basic trends until that time are documented. Overharvesting in the 19th century eradicated the population on the Kuril Islands where Northern Fur Seals were considered extinct until the mid 1950s. Pup production grew rapidly on the Kurils during 1962-1977 (19.9% annual increase). The population stabilized around 1978 and trend became slightly negative (-0.8%) during 1978-1988. Pup production in the Kuril Islands has increased 82.4% since 1988 (+3.8% annually) and is now comparable to the Tuleny (Robben) Island population. During the last count in 2006, approximately 27,090 pups were counted. Total abundance of Fur Seals in the Kuril Islands currently exceeds 100,000 individuals (Kuzin 1999).

In 1999, A. Kuzin published a detailed description of the biology and history of Northern Fur Seals in Russia with special emphasis on Tuleny Island. He reported that the population at Tuleny at the time of its discovery in 1852 was approximately 120,000. Subsequent unregulated harvest reduced the population to as low as a few thousand animals in the late 1890s. Tuleny Island then underwent a series of population highs and low during various periods of harvest. The maximum population was approximately 180,000 individuals in the late 1960s (Kuzin 1999). The most recent estimate was 140,000 individuals including 42,200 pups in 2009 (Kuzin 2010).

The San Miguel stock of Northern Fur Seals breeds primarily on San Miguel Island, California, at the southern extent of the breeding range. This population has increased or been stable since its discovery in 1968 (Caretta et al. 2013). The trend in pup births includes a steady increase followed by a sharp decline that has been shown to be directly tied to El Niño events; pup production in 1997-1998 declined 81% due to the redistribution of prey caused by the event. Overwinter satellite telemetry studies have shown that Northern Fur Seals from all of the US breeding sites use similar foraging grounds along the west coast of Southeast Alaska, British Columbia, Washington and Oregon (Lea et al. 2009, Ream et al. 2005, Sterling and Ream 2004). The overlap is not limited to foraging habitat as genetic studies indicate that there is very little differentiation between animals throughout the range (Dickerson et al. 2010).

Population estimates for Northern Fur Seals are generally derived by multiplying pup counts by a correction factor of 4.4747 to include all non-pups. A global abundance estimate was generated from the most recently available count and estimate data for all subpopulations in the range using the agTrend model (Johnson and Fritz 2014). The 2014 estimate for localities other than the Pribilofs is a projected number based on the trends at each site. The modelled population estimate used all of the data available since 1966 to project the estimates reported above. The most recent actual count and estimated numbers used in the model are shown below.

Pribilof Islands, 2014

St. Paul Island: 91,737 pups x 4.4747 = 410,496 (Towell et al. 2014)

St. George Island: 18,937 pups x 4.474 = 84,737 (Towell et al. 2014)

Sea Lion Rock: 5,250 pups x 4.4747 = 23,492 (Towell et al. 2014)

Commander Islands, 2006: 59,805 x 4.4747 = 267,609 (Burkanov and Calkins 2007)

Tuleny Island, 2009: 42,200 x 4.4747 = 188,832 (Kuzin 2010)

Kuril Islands, 2006: 25,164 pups x 4.4747 = 112,601(Burkanov et al. 2007)

Bogoslof Island, 2011: 22,905 pups x 4.4747 = 102,493 (Towell et al. 2012)

San Miguel Island, 2014 (not including Castle Rock): 2,327 x 4.4747 = 10,412 (A. Orr, NMFS pers. comm.)

Farallon Islands, 2014: 656 pups x 4.4747 = 2,935 (R. Berger, Point Blue Conservation Science pers. comm.)

The global population of Northern Fur Seals is estimated to be approximately 1.29 million in 2014, a decline of approximately 658,000 since 1976. Note that this number is different than the sum of abundances given above because most were projected forward to 2014 in the model. Using the agTrend model to project the population reduction at all sites over the past three generations (1972-2014) gives an estimated reduction of 30.1% (95% CI -47.1% to 14.5%). Annual abundance estimates for the entire range do not exist as there are no consistent monitoring strategies in place. Although abundance is declining, the overall decline is not proportional across all sites. The greatest decreases are occurring in the Pribilof Islands, while populations in the Kuril Islands and Tuleny Island in Russia, and on Bogoslof Island in Alaska have increased.

The decline described above understates the total reduction of the Northern Fur Seal population in historic times. It is estimated that the population numbered up to 2.5 million animals in the 1950s, and it may have been considerably larger than that when there were many more active rookeries before the onset of human exploitation.

To date the only population viability analysis conducted for Northern Fur Seals was described in a report from the Canadian Science Advisory Secretariat, Department of Fisheries and Oceans, Canada (Olesiuk 2012). This analysis concluded that all subpopulations are presently secure with little risk (0.00%-0.42%) of extirpation within the next century.

Menaces identifiées(5 menaces classées CMP-IUCN)

  • 5_4_2
    Intentional use: (large scale) [harvest]
    Causing/Could cause fluctuationsMajority (50-90%)Past, Unlikely to Return
  • 5_4_4
    Unintentional effects: (large scale) [harvest]
    Causing/Could cause fluctuationsMajority (50-90%)Ongoing
  • 9_2_1
    Oil spills
    Causing/Could cause fluctuationsMinority (<50%)Future
  • 11_1
    Habitat shifting & alteration
    Slow, Significant DeclinesWhole (>90%)Future
  • 5_4_1
    Intentional use: (subsistence/small scale) [harvest]
    No declineMinority (<50%)Ongoing
Description complète des menacesExpert
Northern Fur Seals have one of the longest and most complex histories of commercial harvesting, which began when the main breeding colonies were discovered in the late 18th century; exploitation continued through until 1984. Numerous international treaties and agreements were put in force over time in efforts to manage this species, and they are no longer harvested commercially. Small numbers are taken annually by Alaska Natives in a subsistence harvest on the Pribilof Islands. Harvest levels are declining and are unlikely to be affecting the status of the Fur Seal population.

Northern Fur Seals compete for Walleye Pollock with one of the largest commercial fisheries world. Measurable annual mortality, especially for juveniles and subadults, is caused by entanglements in derelict and discarded fishing gear, marine debris and direct interactions with commercial fisheries. This mortality was highest during the period of active high seas drift net fishing in the North Pacific in the 1980s, but entanglement in debris is an ongoing problem. Long-term ecosystem regime change in the North Pacific and possible changes in the foraging patterns of a key predator (the Killer Whale), may be working synergistically with the fisheries related issues to cause the current population decline.

Like all fur seals, Northern Fur Seals are vulnerable to oil spills because of their dependence on their thick pelage for thermoregulation. The small colonies at San Miguel Island in the California Channel Islands and on the Farallon Island may be at greatest risk due to proximity to major harbours, shipping lanes and offshore oil extraction facilities.

The effect of global climate change on Northern Fur Seals is uncertain. However, any further negative disruption of their ecosystem should be considered a threat.

Habitats préférentiels (classification IUCN)

  • 10_1Marine Oceanic - Epipelagic (0-200m)
  • 12_1Marine Intertidal - Rocky Shoreline
  • 13_1Marine Coastal/Supratidal - Sea Cliffs and Rocky Offshore Islands
  • 9_1Marine Neritic - Pelagic
Mesures de conservation recommandéesExpert
Following the termination of the Interim Convention on the Conservation of the North Pacific Fur Seal in 1984, the Northern Fur Seal is now managed on land independently by the Russian Commonwealth of Independent States and the United States. The eastern north Pacific stock of the Northern Fur Seal was listed as depleted under the U.S. Marine Mammal Protection Act in 1988, and a final conservation plan was completed in December 2007.
Actions de conservation (1)Expert
  • 2_1Site/area management
Stress écologiques (6)Expert
  • 1_2Ecosystem degradation
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_2Species disturbance
Usage & commerce (2)Expert
  • 1Food - human
    subsistance
  • 10Wearing apparel, accessories
    subsistance
Priorités de recherche (6)Expert
  • 1_2Population size, distribution & trends
  • 1_3Life history & ecology
  • 1_4Harvest, use & livelihoods
  • 1_5Threats
  • 1_6Actions
  • 3_1Population trends
Niche IUCN globaleExpert

Royaumes biogéographiques

NearcticPalearctic

Systèmes (terrestre/eau douce/marin)

TerrestrialMarine

Large Marine Ecosystems (LMEs)

Beaufort SeaChukchi SeaEastern Bering SeaWestern Bering SeaKuroshio CurrentOyashio CurrentGulf of AlaskaEast China SeaCalifornia CurrentSea of JapanSea of Okhotsk

Zones de pêche FAO

Pacific - northwestPacific - northeastPacific - eastern central
Références bibliographiques (30)Expert
  1. IUCN. 2015. The IUCN Red List of Threatened Species. Version 2015-4. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 19 November 2015).
  2. Sterling, J.T., Springer, A.M., Iverson, S.J., Johnson, S.P., Pelland, N.A., Johnson D.S., Lea, M.A. and Bond, N.A. 2014. The Sun, Moon, Wind, and Biological Imperative–Shaping Contrasting Wintertime Migration and Foraging Strategies of Adult Male and Female northern fur seals (<i>Callorhinus ursinus</i>). <i>PLoS ONE</i> 9(4): e93068.
  3. Johnson, D.S. and Fritz, L. 2014. agTrend: a Bayesian approach for estimating trends of aggregated abundance. <i>Methods in Ecology and Evolution</i> 5: 1110-1115.
  4. Allen, B.M. and Angliss R.P. 2014. Alaska marine mammal stock assessments, 2013. U.S Department of Commerce National Marine Fisheries Service Technical Memorandum NMFSAFSC-277.
  5. Kuhn, C.E., Baker, J.D., Towell, R.G. and Ream, R.R. 2014. Evidence of localized resource depletion following a natural colonization event by a large marine predator. <i>Journal of Animal Ecology</i> doi: 10.1111/1365-2656.12202.
  6. Towell, R., Ream, R., Bengtson, J. and Sterling, J. 2014. 2014 northern fur seal pup production and adult male counts on the Pribilof Islands, Alaska. Memo to the record. Available at: <a href="http://www.afsc.noaa.gov/nmml/PDF/2014-nfs-pup-counts-pribs.pdf">http://www.afsc.noaa.gov/nmml/PDF/2014-nfs-pup-counts-pribs.pdf</a>.
  7. Pacifici, M., Santini, L., Di Marco, M., Baisero, D., Francucci, L., Grottolo Marasini, G., Visconti, P. and Rondinini, C. 2013. Generation length for mammals. <i>Nature Conservation</i> 5: 87–94.
  8. Towell, R. and Ream, R. 2012. 2011 northern fur seal pup production estimates on Bogoslof Island, Alaska. Memo to the record. Available at: <a href="http://www.afsc.noaa.gov/nmml/PDF/BogPupMem11_final.pdf">http://www.afsc.noaa.gov/nmml/PDF/BogPupMem11_final.pdf</a>.
  9. Olesiuk, P.F. 2012. Population viability analysis for northern fur seals (<i>Callorhinus ursinus</i>) in Canada. Department of Fisheries and Oceans Canada Canadian Science Advisory Secretariat Research Document 2012/041.
  10. Zeppelin, T.K. and Orr, A.J. 2010. Stable isotope and scat analyses indicate diet and habitat partitioning in northern fur seals <i>Callorhinus ursinus</i> across the eastern Pacific. <i>Marine Ecology Progress Series</i> 409: 241-253.
  11. Kuzin, A.E. 2010. The intrapopulation structure of the northern fur seal <i>(Callorhinus ursinus</i> L.) on Tyuleniy Island during the post-depression years (1993–2009). <i>Russian Journal of Marine Biology</i> 36: 507-517.
  12. Dickerson, B.R., Ream, R.R., Vignieri, S.N. and Bentzen, P. 2010. Population structure as revealed by mtDNA and microsatellites in northern fur seals, <i>Callorhinus ursinus</i>, throughout their range. <i>PLoS ONE</i> 5(5): e10671.
  13. Angliss, R.P. and Allen, B.M. 2009. Alaska marine mammal stock assessments, 2008. U.S. Department of Commerce, NOAA Technical Memorandum NMFS-AFSC-193.
  14. Lea, M.A., Johnson, D., Ream, R., Sterling, J., Melin, S. and Gelatt T. 2009. Extreme weather events influence dispersal of naive northern fur seals. <i>Biological Letters</i> 5: 252-257.
  15. National Marine Fisheries Service. 2007. Conservation plan for the Eastern Pacific stock of northern fur seal (<i>Callorhinus ursinus</i>). National Marine Fisheries Service, Juneau, Alaska.
  16. Burkanov, V., Altukhov, A., Andrews, R., et al. 2007. Northern fur seal (<i>Callorhinus ursinus</i>) pup production in the Kuril Islands, 2005-2006. 17th Biennial Conference on the Biology of Marine Mammals. Cape Town, South Africa.
  17. Burkanov, V. and Calkins, D. 2007. Overview of abundance and trends of northern fur seal (<i>Callorhinus ursinus</i>) in Commander Islands, 1958-2006, caveats and conclusions. Alaska Marine Science Symposium. Anchorage, Alaska.
  18. Ream, R.R., Sterling, J.T. and Loughlin, T.R. 2005. Oceanographic features related to northern fur seal migratory movements. <i>Deep-Sea Research II</i> 52: 823-843.
  19. Sterling J.T. and Ream, R.R. 2004. At-sea behavior of juvenile male fur seals (<i>Callorhinus ursinus</i>). <i>Canadian Journal of Zoology</i> 82: 1621-1637.
  20. Ream, R.R., Baker, J.D. and Towell, R.G. 1999. Bogoslof Island Studies, 1997. In: E.H. Sinclair and B.W. Robson (eds), Fur Seal Investigations, 1997. U.S. Department of Commerce, NOAA Technical Memorandum NMFS-AFSC-106..
  21. Kuzin, A..E. 1999. The northern fur seal. Russian Marine Mammal Council Pacific Fishery and Oceanography Research Center .
  22. Rice, D.W. 1998. <i>Marine Mammals of the World: Systematics and Distribution</i>. Society for Marine Mammalogy, Special Publication Number 4, Lawrence, Kansas.
  23. Gentry, R. L. 1998. <i>Behavior and ecology of the northern fur seal</i>. Princeton University Press, Princeton, New Jersey, USA.
  24. York, A.E. and Scheffer, V.B. 1997. Timing of implantation in the northern fur seal, <i>Callorhinus ursinus</i>. <i>Journal of Mammalogy</i> 78: 675-683.
  25. Loughlin, T.R., Antonelis, G.A., Baker, J.D., York, A.E., Fowler, C.W., DeLong, R.L. and Braham, H.W. 1994. Status of the northern fur seal population in the United States during 1992. In: E.H. Sinclair (ed.), Fur Seal Investigations, 1992. U.S. Department of Commerce, NOAA Technical Memorandum NMFS-AFSC-45:9-28.
  26. Loughlin, T.R. and Miller, R.V. 1989. Growth of the northern fur seal colony on Bogoslof Island, Alaska. <i>Arctic</i> 42: 368-372.
  27. Roppel, A.Y. 1984. Management of northern fur seals on the Pribilof Islands, Alaska, 1786-1981. U.S. Department of Commerce, NOAA Technical Report NMFS-4.
  28. Lloyd, D.S., McRoy, C.P. and Day, R.H. 1981. Discovery of northern fur se<i>als (Callorhinus ursinus</i>) breeding on Bogoslof Island, Southeastern Bering Sea. <i>Arctic</i> 34: 316-320.
  29. York, A.E. and Hartley, J.R. 1981. On the estimation of numbers of northern fur seal, <i>Callorhinus ursinus</i>, pups born on St. Paul Island, 1980-86. <i>Fishery Bulletin</i> 85: 367-375.
  30. Roppel, A.Y. and Davey, S.P. 1965. Evolution of fur seal management on the Pribilof Islands. <i>Journal of Wildlife Management</i> 29: 448-463.
Évaluateurs & contributeurs (3)Expert
assessor
Gelatt, T., Ream, R. & Johnson, D.
evaluator
Lowry, L.
facilitators
Lowry, L., Ahonen, H., Pollock, C.M., Chiozza, F. & Battistoni, A.

Gelatt, T., Ream, R. & Johnson, D. 2015. Callorhinus ursinus. The IUCN Red List of Threatened Species 2015: e.T3590A45224953. Accessed on 05 May 2026.

Traits biologiques

21 valeurs · 8 sources

Morphologie(5)

Masse adulte
166 kg
AnAge
Masse cerveau
319 g
AnimalTraits
Masse naissance
5,3 kg
AnAge
Masse au sevrage
12,9 kg
AnAge
Longueur
1,7 m
PanTHERIA

Cycle de vie(1)

Longévité max
35 ans
PanTHERIA
Voir 15 traits de plus (2 catégories)

Reproduction(6)

Sevrage
3,5 mois
AnAge
Taille de portée
1
AnAge
Maturité sexuelle
5,5 ans
AnAge
Portées par an
1
AnAge
Gestation
7,9 mois
AnAge
Intervalle naissances
1 ans
AnAge

Écologie & habitat(9)

Invertébrés (%)
40 %
elton_mammals
Graines (%)
0 %
elton_mammals
Fruits (%)
0 %
elton_mammals
Nectar (%)
0 %
elton_mammals
Charognard (%)
0 %
elton_mammals
Poissons (%)
60 %
elton_mammals
Autre végétal (%)
0 %
elton_mammals
Vert. ectothermes (%)
0 %
elton_mammals
Vert. endothermes (%)
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

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

Consulter sur les bases externes

Observations & statuts

Cartographie

Bibliographie

Note nomenclaturale & synonymesExpert

Note nomenclaturale

TAXREF v18 — INPN/MNHN

Synonymes (11)— redirigent vers cette page

  • Arctocephalus californianusGray, 1866
  • Arctocephalus ursinusLinnaeus, 1758
  • Callorhinus alascanusJordan & Clark, 1898
  • Callorhinus curilensisJordan & Clark, 1899
  • Otaria krachenninikowiiLesson, 1828
  • Otoes ursinusKuroda, 1938
  • Otoes ursinus curilensisEllerman & Morrison-Scott, 1951
  • Phoca minimaTilesius, 1835
  • Phoca nigraPallas, 1811
  • Phoca ursinaLinnaeus, 1758
  • Siren cynocephalaWalbaum, 1792

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