Ontologia
Phogue du Groenland

Phogue du Groenland

Pagophilus groenlandicus(Erxleben, 1777)

NTLR Monde (IUCN)
  1. Animal
  2. Chordata
  3. Mammalia
  4. Carnivora
  5. Phocidae
1 photo · 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 Pagophilus groenlandicus 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

99 partenaires écologiques documentés directement dans GloBI.

Partenaires
99
Espèces avec interactions documentées
Types d'interactions
8
Prédation, pollinisation, parasitisme…
Connectance
0.077
Densité des liens dans le sous-graphe affiché
Rang animalia
97 %
Percentile vs ensemble des animalia

Liste rouge IUCN

NT · Quasi menacéecritères A3cDécroissante
Évaluation complète
Évaluation
2025 · v3.1
Altitude
0 m
Profondeur
4000 m
État de la populationExpert
All three Harp Seal populations have been assessed recently (although new surveys are not available for the White Sea). Recent pup production surveys have been carried out in the Greenland Sea in 2012, 2018 and 2022. A total of 54,181 (95% CI: 36,078–72,284) pups were estimated to have been born in 2018 and 92,769 (CV 20.2) in 2022, returning to a level similar to the 2012 survey (89,590, CV 0 13.7%; ICES 2023). These estimates are significantly lower than estimates obtained in similar surveys in 2002 and 2007. The estimated population size according to the 2018 survey was 426,800 (95% CI 313,000 – 540,600; ICES 2019). Model fitting issues and uncertainty about the available reproductive data did not allow for a new estimate to be created with the most recent data, so the current trend for this population is unknown (ICES 2023). The White Sea/Barents Sea Harp Seal population has not been surveyed since 2013. However, abundance-based upon the existing time series of pup production estimates, fecundity and removals suggest a population size of 1,497,000 (95% CI 1,293,000–1,701,000), which suggests a stable trend (ICES 2019, 2023).

The Northwest Atlantic population was assessed in 2023 based on pup production surveys carried out in 2017 (ICES 2023). Pup production was estimated to be 746,500 (95% CI 572,000 - 922,500), which is the lowest since 1994, although not significantly different from the previous survey in 2012 (Stenson et al. 2020). The total Northwest Atlantic population was estimated to be 7.6 million (95% CI 6.6 – 8.8 million) in 2019 (Hammill et al. 2021) and the trend is either stable or increasing slightly (ICES 2023).

A small whelping patch was found near South Greenland in 2007 (Rosing-Asvid 2008), but the source of these animals and the inter-annual stability of this group is not known. However, this finding is particularly interesting in light of climate change.

Menaces identifiées(5 menaces classées CMP-IUCN)

  • 11_1
    Habitat shifting & alteration
    Rapid DeclinesWhole (>90%)Ongoing
  • 11_5
    Other impacts
    Rapid DeclinesWhole (>90%)Ongoing
  • 5_4_2
    Intentional use: (large scale) [harvest]
    Rapid DeclinesMajority (50-90%)Past, Unlikely to Return
  • 5_4_1
    Intentional use: (subsistence/small scale) [harvest]
    Negligible declinesWhole (>90%)Ongoing
  • 5_4_4
    Unintentional effects: (large scale) [harvest]
    Slow, Significant DeclinesUnknownOngoing
Description complète des menacesExpert
Harp Seals have been harvested for thousands of years by native peoples of the North Atlantic, including coastal Northern Europeans historically when the species occurred in the Baltic (Stora and Ericson 2004). Basque whalers began taking Harp Seals in more northerly waters in the 1500s. By the mid-1600s, French settlers began the hunt in the Gulf of St Lawrence, developing land-based netting techniques on the St Lawrence River in the 1700s. By the 1800s, schooner-based sealing developed, and the number of seals harvested rose dramatically in the Northwest Atlantic; from 1803-1816 the average annual was 117,000 specimens. The peak of sealing in the Northwest Atlantic occurred between 1818 and 1862, when 500,000 seals per year were harvested in many years, reaching maximum peeks of 640,000-740,000 in single years. During that time, it is estimated that 18.3 million harp seals, mostly whitecoats, were killed for oil. There was also early commercial harvesting in the Northeast Atlantic, though at somewhat lower levels. At Jan Mayen, the catch began falling in the late 1850s, likely due to overharvesting and population depression. From 1860 to 1900, an estimated 12.8 million seals were harvested from the West Ice (Lavigne and Kovacs 1988).

The 20th century saw the advent of steel-hulled ships, and the hunt continued, though Harp Seals became more valued for their pelts than their oil. The size of all three Harp Seal populations has fluctuated through time, driven largely by the size of the commercial harvests (Sergeant 1976). In 1983, the European Economic Community imposed an import ban on seal products, because of public reactions to the white-coat harvest and the average annual commercial harvests fell precipitously. Indigenous groups lobbied the EU parliament successfully and in 2009 exemptions were made for subsistence harvest products. Greenlandic subsistence catches of Harp Seals vastly outnumber commercial harvests in recent decades. Greenland took 50,000-100,00 Harp Seals annually in the 1990s and 2000s (https://nammco.no/catch-database). Harvests in the last decade average some 40,000. Norwegian catches for the West Ice are generally under 10,000 animals per year and little hunting occurs in the White Sea.

Capelin collapses in the Barents Region in the 1980s resulted in Harp Seals shifting their distribution southward and foraging along the coast of Norway, resulting in several major mortality events in shore-based net fisheries. Bycatch mortality from nets was estimated to be 56,647 (perhaps up to 100,000) in 1987, and 21,474 in 1988 though it is thought that actually mortalities might have exceeded 100,000 in each of these years (Haug et al. 1991). These events demonstrated the potential risk that fisheries represent to Harp Seals. A major assessment of fisheries catches vs marine mammal consumption suggests that there is strong potential for direct competition between fisheries and pinnipeds (and other marine mammals) in the Greenland Sea, while competition in the Barents Sea is likely not currently an issue (Skern-Mauritzen et al. 2022).

A major threat to Harp Seals is climate warming (Laidre et al. 2008, 2015, Kovacs et al. 2011, 2012, 2021) which is already impacting all populations through reductions in their drift ice breeding habitats and likely via indirect impacts on their prey populations as well. Recently there have been years with very high pup mortalities because of low ice availability and great variability and generally low survivorship seem to be the new norm (Johnston et al. 2005, Bajzak et al. 2011, Stenson and Hammill 2014, Hammill et al. 2015, 2021, Stenson et al. 2020). In North America, years with high stranding numbers are correlated with environmental conditions, including warm temperatures and little sea ice (Haverkamp et al. 2023). Shifts have occurred in the location of whelping locations in the Greenland Sea and in the Northwest Atlantic during years when ice conditions have been extremely poor (Rosing-Asvid 2008, Stenson et al. 2016, 2020). When pupping occurs outside the traditional areas, the young may be exposed to ice that is less stable and to different prey fields during the period when they are first learning to find food. In the Greenland Sea and in areas off Newfoundland, increased predation from Polar Bears which travel great distances to seek out the pupping concentrations (Peacock et al. 2013) might become a significant survivorship issue. Other changes include shifts in abundance and distribution of many key prey species for Harp Seals which has negatively impacted body condition and reproductive rates in all populations (Øigård et al. 2013, Stenson et al. 2020). Large Atlantic cod stocks in the Northeast Atlantic are likely competing with Harp Seals for prey (Bogstad et al. 2015, Stenson et al. 2020) and the overall borealisation and base-line nutrient shifts in the Barents Sea is likely to continue to negatively impact Harp Seal’s traditional Arctic fish and invertebrate prey populations (Fossheim et al. 2015, de la Vega et al. 2022).

Habitats préférentiels (classification IUCN)

  • 9Marine Neritic
Mesures de conservation recommandéesExpert
In the Northeast Atlantic, quotas for Harp Seals are set by the Joint Norwegian/Russian Commission, based on recommendations made by the International Council for Exploration of the Sea (see ICES 2019, 2023). White-coated pups are protected in Norway and Russia. However, there are no quotas in Greenland.

Further research into the population trend of this species is recommended.
Actions de conservation (1)Expert
  • 1_1Site/area protection
Stress écologiques (10)Expert
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_2Species disturbance
  • 2_3_7Reduced reproductive success
  • 2_3_8Other
Usage & commerce (1)Expert
  • 17Other (free text)
    internationalnationalsubsistance
Priorités de recherche (1)Expert
  • 1_2Population size, distribution & trends
Niche IUCN globaleExpert

Royaumes biogéographiques

Palearctic

Systèmes (terrestre/eau douce/marin)

Marine

Zones de pêche FAO

Arctic SeaAtlantic - northwestAtlantic - northeast
Références bibliographiques (30)Expert
  1. IUCN. 2025. The IUCN Red List of Threatened Species. Version 2025-1. Available at: <a href="www.iucnredlist.org">www.iucnredlist.org</a>. (Accessed: 27 March 2025).
  2. Haverkamp, H., Chang, H.Y., Newcomb, E., Doughty, L., Walk, D., Seton, R., Jones, L.S., Todd, S. and Cammen, K.M. 2023. A retrospective socio-ecological analysis of seal strandings in the Gulf of Maine. <i>Marine Mammal Science</i> 39: 232-250.
  3. ICES. 2023. Report of the Joint ICES/NAFO/NAMMCO Working Group on Harp and Hooded Seals (WGHARP). <i>ICES Scientific Reports</i> 5(96): 1-75 pp. https://doi.org/10.17895/ices.pub.24306100
  4. de la Vega, C., Buchanan, P.J., Tagliabue, A., Hopkins, J.E., Jeffreys, R.M., Frie, A.K., Biuw, M., Kershaw, J., Grecian, J., Norman, L., Smout, S., Haug, T. and Mahaffey, C. 2022. Multi-decadal environmental change in the Barents Sea recorded by seal teeth. <i>Global Change Biology</i> 28: 3054-3065.
  5. Skern-Mauritzen, M., Lindstrøm, U., Biuw, M., Elvarsson, B., Gunnlaugsson, T., Haug, T., Kovacs, K.M., Lydersen, C., McBride, M.M., Mikkelsen, B., Øien N. and Víkingsson, G. 2022. Marine mammal consumption and fisheries removals in the Nordic and Barents seas. <i>ICES Journal of Marine Sciences</i> 79: 1583-1603.
  6. Hamilton, C.D., Lydersen, C., Aars, J., Biuw, M., Boltunov, A.N., Born, E.W., Dietz, R., Folkow, L.P., Glazov, D.M., Haug, T., Heide-Jørgensen, M.P., Kettemer, L.E., Laidre, K.L., Øien, N., Nordøy, E.S., Rikardsen, A.H., Rosing-Asvid, A., Semenova, V., Shpak, O.V., Svegaard, S., Ugarte, F., Wiig, Ø. and Kovacs, K.M. 2021. Marine mammal hotspots in the Greenland and Barents Seas. <i>Marine Ecology Progress Series </i> 659: 3-28.
  7. Hammill, M.O., Stenson, G.B., Mosnier, A. and Doniol-Valcroze, T. 2021. Trends in abundance of harp seal, <i>Pagophilus groenlandicus</i>, in the Northwest Atlantic, 1952-2019. DFO Can. Sci. Advis. Sec. Research Document 2021/006.
  8. Kovacs, K.M., Belikov, S., Boveng, P., Desportes, G., Ferguson, S., Hansen, R., Laidre, K., Stenson, G., Thomas, P., Ugarte, F. and Vongraven, D. 2021. 2021 State of the Arctic Marine Biodiversity Report (SAMBR) Update: 2021. Technical Report. Conservation of Arctic Flora and Fauna International Secretariat. Akureyri, Iceland.
  9. Stenson, G.B., Haug, T. and Hammill, M.O. 2020. Harp seals: monitors of change in differing ecosystems. <i>Frontiers in Marine Science</i> 7: https://doi.org/10.3389/fmars.2020.569258
  10. ICES. 2019. ICES/NAFO/NAMMCO Working Group on Harp and Hooded Seals (WGHARP). ICES Scientific Reports 1:72. International Council for the Exploration of the Sea (ICES).
  11. Enoksen, S., Haug, T., Lindstrøm, U. and Nilssen, K.T. 2017. Recent summer diet of hooded <i>Cystophora cristata</i> and harp <i>Pagophilus groenlandicus</i> seals in the drift ice of the Greenland Sea. <i>Polar Biology</i> 40: 931-937.
  12. Stenson, G.B., Buren, A.D. and Koen-Alonso, M. 2016. The impact of changing climate and abundance on reproduction in an ice-dependent species, the Northwest Atlantic harp seal, <i>Pagophilus groenlandicus</i>. <i>ICES Journal of Marine Sciences</i> 73: 250-262.
  13. Hammill, M.O., Stenson, G.B., Doniol-Valcroze, T. and Mosnier, A. 2015. Conservation of Northwest Atlantic harp seals: past success, future uncertainty. <i>Biological Conservation</i> 192: 181-191.
  14. Carr, S.M., Duggan, A.T., Stenson, G.B. and Marshall, H.D. 2015. Quantitative phylogenomics of within-species mitogenome variation: Monte Carlo and non-parametric analysis of phylogeographic structure among discrete transatlantic breeding areas of harp seals (<i>Pagophilus groenlandicus</i>). <i>PLOS ONE</i> 10(8): https://doi.org/10.1371/journal.pone.0134207
  15. Bogstad, B., Gjøsæter, H., Haug, T. and Lindstrøm, U. 2015. A review of the battle for food in the Barents Sea: cod vs marine mammals. <i>Frontiers in Ecology and Evolution</i> 3(29): https://doi.org/10.3389/fevo.2015.00029
  16. Fossheim, M., Primicderio, R., Johannesen, E., Ingvaldsen, R.B., Aschan, M.M. and Dolgov, A.V. 2015. Recent warming leads to a rapid borealization of fish communities in the Arctic. <i>Nature Climate Change</i> doi:10.1038/NCLIMATE2647.
  17. Laidre, K.L., Stern, H., Kovacs, K.M., Lowry, L., Moore, S.E., Regehr, E.R., Ferguson, S.H., Wiig, Ø., Boveng, P., Angliss, R.P., Born, E.W., Litovka, D., Quakenbush, L., Lydersen, C., Vongraven, D. and Ugarte, F. 2015. Arctic marine mammal population status, sea ice habitat loss, and conservation recommendations for the 21st century. <i>Conservation Biology</i> 29: 724-737.
  18. Øigård, T.A., Haug, T. and Nilssen, K.T. 2014. From pup production to quotas: current status of harp seals in the Greenland Sea. <i>ICES Journal of Marine Science</i> 71: 537-545.
  19. Stenson, G.B. and Hammill, M.O. 2014. Can ice breeding seals adapt to habitat loss in a time of climate change? <i>ICES Journal of Marine Science</i> 71: 1977-1986.
  20. Peacock, E., Taylor, M.K., Laake, J. and Stirling, I. 2013. Population ecology of polar bears in Davis Strait, Canada and Greenland. <i>Journal of Wildlife Management</i> 77: 463-476.
  21. Øigård, T.A., Lindstrom, U., Haug, T., Nilssen, K.T. and Smout, S. 2013. Functional relationship between harp seal body condition and available prey in the Barents Sea. <i>Marine Ecology Progress Series</i> 484: 287-307.
  22. Lindstrom, U., Nilssen K.T., Pettersen L.M.S. and Haug, T. 2013. Harp seal foraging behaviour during summer around Svalbard in the northern Barents Sea: diet composition and the selection of prey. <i>Polar Biology</i> 36(305-320).
  23. Kovacs, K.M., Aguilar, A., Aurioles, D., Burkanov, V., Campagna, C., Gales, N.J., Gelatt, T., Goldsworthy, S.D., Goodman, S.J., Hofmeyr, G.J.G., Härkönen, T., Lowry, L., Lydersen, L., Schipper, J., Sipilä, T., Southwell, C., Thompson, D. and Trillmich, F. 2012. Global threats to pinnipeds. <i>Marine Mammal Science</i> 28: 414-436.
  24. Berta, A. and Churchill, M. 2011. Pinniped taxonomy: review of currently recognized species and subspecies, and evidence used for their description. <i>Mammal Review</i> 42: 207-234.
  25. Bajzak, C.E., Hammill, M.O., Stenson, G.B. and Prinseenberg, S. 2011. Drifting away: Implications of changes in ice conditions for a pack-ice breeding phocid, the harp seal (<i>Pagophilus groenlandicus</i>). <i>Canadian Journal of Zoology</i> 89: 1050-1062.
  26. Kovacs, K.M., Moore, S., Overland, J.E. and Lydersen, C. 2011. Impacts of changing sea-ice conditions on Arctic marine mammals. <i>Marine Biodiversity</i> 41: 181-194.
  27. Nordøy, E.S., Folkov, L.P., Potelov, V. and Prischemikhin, V. 2008. Seasonal distribution and dive behaviour of harp seals (<i>Pagophilus groenlandicus</i>) of the White Sea- Barents Sea stock. <i>Polar Biology</i> 31: 1119-1135. https://doi.org/10.1007/s00300-008-0453-9
  28. Rosing-Asvid, A. 2008. A new harp seal whelping ground near South Greenland. <i>Marine Mammal Science</i> 24: 730-736.
  29. Laidre, K.L., Stirling, I., Lowry, L.F., Wiig, Ø., Heide-Jørgensen, M.P. and Ferguson, S.H. 2008. Quantifying the sensitivity of Arctic marine mammals to climate‐induced habitat change. <i>Ecological Applications</i> 18: 97-125.
  30. Anon. Fisheries and Oceans Canada (DFO). 2005. <i>Atlantic Seal Hunt 2003 Management Plan, at http://www.dfo-mpo.gc.ca/seal-phoque/reports-rapports/mgtplan-plangest2003/mgtplan-plangest2003_e.htm.</i>.
Évaluateurs & contributeurs (2)Expert
assessor
Kovacs, K.M.
evaluator
Stenson, G. & Bellotto, V.

Kovacs, K.M. 2025. Pagophilus groenlandicus (Europe assessment). The IUCN Red List of Threatened Species 2025: e.T41671A212940648. Accessed on 05 May 2026.

Traits biologiques

22 valeurs · 7 sources

Morphologie(5)

Masse adulte
180 kg
AnAge
Masse cerveau
275 g
AnimalTraits
Masse naissance
8,7 kg
AnAge
Masse au sevrage
34,6 kg
AnAge
Longueur
1,7 m
PanTHERIA

Cycle de vie(1)

Longévité max
42 ans
PanTHERIA
Voir 16 traits de plus (3 catégories)

Reproduction(6)

Sevrage
1,7 sem.
AnAge
Taille de portée
1
AnAge
Maturité sexuelle
5 ans
AnAge
Portées par an
-999
PanTHERIA
Gestation
7,5 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

Divers(1)

Température corporelle
36,3 °C
AnAge

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 (9)— redirigent vers cette page

  • Pagophilus groenlandicus groenlandicus(Erxleben, 1777)
  • Pagophilus groenlandicus oceanicus(Lepechin, 1778)
  • Phoca albicaudaDesmarest, 1822
  • Phoca albiniAlessandrini, 1851
  • Phoca groenlandicaErxleben, 1777
  • Phoca groenlica
  • Phoca leucoplaThienemann, 1824
  • Phoca oceanicaLepechin, 1778
  • Phoca semilunarisBoddaert, 1785

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