
Otarie a fourrure
Callorhinus ursinus(Linnaeus, 1758)
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.
Liste rouge IUCN
VU · Vulnérablecritères A2b↘Décroissante- Évaluation
- 2015 · v3.1
- Altitude
- – 10 m
- Profondeur
- 207 – m
État de la populationTexte officiel évaluation IUCNExpert
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_2Intentional use: (large scale) [harvest]Causing/Could cause fluctuationsMajority (50-90%)Past, Unlikely to Return5_4_4Unintentional effects: (large scale) [harvest]Causing/Could cause fluctuationsMajority (50-90%)Ongoing9_2_1Oil spillsCausing/Could cause fluctuationsMinority (<50%)Future11_1Habitat shifting & alterationSlow, Significant DeclinesWhole (>90%)Future5_4_1Intentional use: (subsistence/small scale) [harvest]No declineMinority (<50%)Ongoing
Description complète des menacesTexte détaillé évaluation IUCNExpert
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 recommandéesStratégies de conservation IUCNExpert
Actions de conservation (1)Conservation Actions Classification Scheme — IUCNExpert
2_1Site/area management
Stress écologiques (6)Stresses Classification — IUCNExpert
1_2Ecosystem degradation2_1Species mortality2_1Species mortality2_1Species mortality2_1Species mortality2_2Species disturbance
Usage & commerce (2)Use & Trade — IUCNExpert
1Food - humansubsistance10Wearing apparel, accessoriessubsistance
Priorités de recherche (6)Research Needed Classification — IUCNExpert
1_2Population size, distribution & trends1_3Life history & ecology1_4Harvest, use & livelihoods1_5Threats1_6Actions3_1Population trends
Niche IUCN globaleRealms · Systems · LMEs · Growth forms · FAOs — biogéographie IUCNExpert
Royaumes biogéographiques
Systèmes (terrestre/eau douce/marin)
Large Marine Ecosystems (LMEs)
Zones de pêche FAO
Références bibliographiques (30)Sources scientifiques de l'évaluation IUCNExpert
- 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).
- 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.
- 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.
- 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.
- 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.
- 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>.
- 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.
- 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>.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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..
- Kuzin, A..E. 1999. The northern fur seal. Russian Marine Mammal Council Pacific Fishery and Oceanography Research Center .
- Rice, D.W. 1998. <i>Marine Mammals of the World: Systematics and Distribution</i>. Society for Marine Mammalogy, Special Publication Number 4, Lawrence, Kansas.
- Gentry, R. L. 1998. <i>Behavior and ecology of the northern fur seal</i>. Princeton University Press, Princeton, New Jersey, USA.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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)Personnes ayant contribué à l'évaluation IUCNExpert
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
Morphologie(5)
Cycle de vie(1)
Voir 15 traits de plus (2 catégories)Replier
Reproduction(6)
Écologie & habitat(9)
Sources priorisées par qualité scientifique (peer-reviewed spécialisées → Wikidata fallback). Unités auto-converties, valeur max retenue en cas de mesures multiples. Méthodologie · Citations.
Répartition mondiale
Aucune observation géoréférencée avec précision suffisante (<10 km) dans GBIF pour cette espèce.
Consulter sur les bases externes
Observations & statuts
Cartographie
Note nomenclaturale & synonymesDétails taxonomiques + synonymes CoLExpert
Note nomenclaturale
TAXREF v18 — INPN/MNHNSynonymes (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).